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1. Paster EV, Villines KA, Hickman DL: Endpoints for mouse abdominal tumor models: refinement of current criteria. Comp Med; 2009 Jun;59(3):234-41

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Endpoints for mouse abdominal tumor models: refinement of current criteria.
  • Accurate, rapid, and noninvasive health assessments are required to establish more appropriate endpoints in mouse cancer models where tumor size is not easily measured.
  • We evaluated potential endpoints in mice with experimentally induced peritoneal lymphoma, an abdominal tumor model, by comparing body weight, body condition, and behavior with those of a control group of mice not developing lymphoma.
  • Our hypothesis was that body weight would increase or plateau, whereas body condition and behavioral scores would decrease, as disease progressed.
  • Our results support the use of body condition and behavioral scoring as adjunctive assessment methods for mice involved in abdominal lymphoma tumor studies in which health may decline despite an increase or plateau in body weight.
  • [MeSH-major] Behavior, Animal. Body Constitution. Disease Models, Animal. Endpoint Determination. Lymphoma, T-Cell / pathology. Peritoneal Neoplasms / pathology

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  • (PMID = 19619413.001).
  • [ISSN] 1532-0820
  • [Journal-full-title] Comparative medicine
  • [ISO-abbreviation] Comp. Med.
  • [Language] eng
  • [Publication-type] Evaluation Studies; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC2733284
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2. Cissé M, Konaté I, Dieng M, Ka O, Dia A, Touré CT: [Giant leiomyoma of fallopian tube: a rare aetiology of abdominal tumor]. J Gynecol Obstet Biol Reprod (Paris); 2008 Dec;37(8):799-801

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Giant leiomyoma of fallopian tube: a rare aetiology of abdominal tumor].
  • [Transliterated title] Léiomyome géant de la trompe utérine: une cause rare de tumeur abdominale.
  • We report a revealed case by a voluminous-abdominal mass in a 35-year-old woman.
  • Neither the tomodensitometry nor, even, the laparoscopy did not permit specifying the tubal origin of the tumor.
  • [MeSH-major] Fallopian Tube Neoplasms / diagnosis. Leiomyoma / diagnosis
  • [MeSH-minor] Abdomen. Adult. Diagnosis, Differential. Female. Humans. Treatment Outcome

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  • (PMID = 18805654.001).
  • [ISSN] 0368-2315
  • [Journal-full-title] Journal de gynécologie, obstétrique et biologie de la reproduction
  • [ISO-abbreviation] J Gynecol Obstet Biol Reprod (Paris)
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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3. Kosugi S, Mizumachi S, Kitajima A, Igarashi T, Hamada T, Kaya H, Kurihara K, Ogasawara K, Sakata H, Yamamoto M, Nagamine M, Yamazaki H: Prostate cancer with supraclavicular lymphadenopathy and bulky abdominal tumor. Intern Med; 2007;46(14):1135-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Prostate cancer with supraclavicular lymphadenopathy and bulky abdominal tumor.
  • A 73-year-old man with suspected lymphoproliferative disorder was introduced to our hospital.
  • The patient demonstrated palpable hard masses in the abdomen.
  • Enhanced computed tomography of the abdomen and pelvis revealed a bulky mass of para-aortic lymph nodes.
  • Serum tumor markers were examined, revealing prostate-specific antigen (PSA) levels of 3,354.0 ng/ml.
  • [MeSH-major] Abdominal Neoplasms / secondary. Adenocarcinoma / secondary. Prostatic Neoplasms / pathology

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  • (PMID = 17634715.001).
  • [ISSN] 1349-7235
  • [Journal-full-title] Internal medicine (Tokyo, Japan)
  • [ISO-abbreviation] Intern. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] EC 3.4.21.77 / Prostate-Specific Antigen
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4. Dedeken P, Louw V, Vandooren AK, Verstegen G, Goossens W, Dubois B: Plumbism or lead intoxication mimicking an abdominal tumor. J Gen Intern Med; 2006 Jun;21(6):C1-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Plumbism or lead intoxication mimicking an abdominal tumor.
  • In this case report, the diagnosis was finally made when bilateral wrist drop developed on top of abdominal cramps and anemia.
  • Before, ascites raised the suspicion of a tumor.
  • Therefore, each element of the triad of unexplained anemia, abdominal cramps, and bilateral wrist (or foot) drop should lead any physician to consider the diagnosis of lead intoxication.
  • [MeSH-major] Abdominal Neoplasms / diagnosis. Lead Poisoning / diagnosis. Lead Poisoning, Nervous System / diagnosis

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  • (PMID = 16808730.001).
  • [ISSN] 1525-1497
  • [Journal-full-title] Journal of general internal medicine
  • [ISO-abbreviation] J Gen Intern Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Chelating Agents; 0 / Protoporphyrins; DX1U2629QE / Succimer
  • [Other-IDs] NLM/ PMC1924641
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5. Ueda S, Yamada Y, Tsuji Y, Kawaguchi R, Haruta S, Shigetomi H, Kanayama S, Yoshida S, Sakata M, Sado T, Kitanaka K, Kobayashi H: Giant abdominal tumor of the ovary. J Obstet Gynaecol Res; 2008 Feb;34(1):108-11
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Giant abdominal tumor of the ovary.
  • A giant abdominal tumor can exert a mass effect on surrounding structures.
  • We report here a 34-year-old single female who presented with an increased abdominal girth and was subsequently found to have a giant abdominal mass.
  • [MeSH-major] Cystadenoma, Serous / diagnosis. Hypotension / prevention & control. Ovarian Neoplasms / diagnosis

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  • (PMID = 18226141.001).
  • [ISSN] 1341-8076
  • [Journal-full-title] The journal of obstetrics and gynaecology research
  • [ISO-abbreviation] J. Obstet. Gynaecol. Res.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Japan
  • [Number-of-references] 12
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6. Poilblanc M, Coquaz S, Welschbillig K, Arnaud JP, Hamy A: [A case report of stromal tumor in the ligamentum teres hepatis]. Gastroenterol Clin Biol; 2006 Mar;30(3):469-70

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [A case report of stromal tumor in the ligamentum teres hepatis].
  • [Transliterated title] Tumeur stromale du ligament rond hépatique. A propos d'un cas.
  • This case report relates to a 73-year old man presenting a large susmesocolic abdominal tumor whose analysis demonstrated to be a stromal tumour of the ligamentum teres hepatis.
  • [MeSH-major] Gastrointestinal Stromal Tumors. Ligaments. Liver

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  • (PMID = 16633315.001).
  • [ISSN] 0399-8320
  • [Journal-full-title] Gastroentérologie clinique et biologique
  • [ISO-abbreviation] Gastroenterol. Clin. Biol.
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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7. Kalapurakal JA, Li SM, Breslow NE, Beckwith JB, Ritchey ML, Shamberger RC, Haase GM, Thomas PR, Grundy P, Green DM, D'Angio GJ: Intraoperative spillage of favorable histology wilms tumor cells: influence of irradiation and chemotherapy regimens on abdominal recurrence. A report from the National Wilms Tumor Study Group. Int J Radiat Oncol Biol Phys; 2010 Jan 1;76(1):201-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Intraoperative spillage of favorable histology wilms tumor cells: influence of irradiation and chemotherapy regimens on abdominal recurrence. A report from the National Wilms Tumor Study Group.
  • PURPOSE: We undertook this study to determine (1) the frequency with which spilled tumor cells of favorable histology produced intra-abdominal disease in patients treated with differing chemotherapy regimens and abdominal radiation therapy (RT) and (2) the patterns of relapse and outcomes in such patients.
  • METHODS AND MATERIALS: The influence of RT dose (0, 10, and 20 Gy), RT fields (flank, whole abdomen), and chemotherapy with dactinomycin and vincristine (2 drugs) vs. added doxorubicin (three drugs) on intra-abdominal tumor recurrence rates was analyzed by logistic regression in 450 patients.
  • CONCLUSIONS: Irradiation (10 Gy or 20 Gy) reduced abdominal tumor recurrence rates after tumor spillage.
  • Tumor spillage in Stage II patients reduced relapse-free survival and overall survival, but only the latter was of statistical significance.
  • These data provide a basis for assessing the risks vs. benefits when considering treatment for children with favorable histology Wilms tumor and surgical spillage.

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  • (PMID = 19395185.001).
  • [ISSN] 1879-355X
  • [Journal-full-title] International journal of radiation oncology, biology, physics
  • [ISO-abbreviation] Int. J. Radiat. Oncol. Biol. Phys.
  • [Language] ENG
  • [Grant] United States / NCI NIH HHS / CA / CA054498-13; United States / NCI NIH HHS / CA / R01 CA054498; United States / NCI NIH HHS / CA / R01 CA054498-13
  • [Publication-type] Journal Article; Randomized Controlled Trial
  • [Publication-country] United States
  • [Chemical-registry-number] 1CC1JFE158 / Dactinomycin; 5J49Q6B70F / Vincristine; 80168379AG / Doxorubicin
  • [Other-IDs] NLM/ NIHMS167454; NLM/ PMC2843421
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8. Cissé M, Konaté I, Ka O, Dieng M, Dia A, Touré CT: Giant splenic pseudocyst, a rare aetiology of abdominal tumor: a case report. Cases J; 2010;3:16

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Giant splenic pseudocyst, a rare aetiology of abdominal tumor: a case report.
  • CASE PRESENTATION: A twenty-year old Senegalese woman, was admitted with a three-month history of spontaneous abdominal mass associated with a pain.

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  • (PMID = 20148140.001).
  • [ISSN] 1757-1626
  • [Journal-full-title] Cases journal
  • [ISO-abbreviation] Cases J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2820005
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9. Günther P, Tröger J, Holland-Cunz S, Behnisch W, Hinz U, Romero P, Schenk JP: Surgical complications in abdominal tumor surgery in children. Experiences at a single oncological center. Eur J Pediatr Surg; 2009 Oct;19(5):297-303
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Surgical complications in abdominal tumor surgery in children. Experiences at a single oncological center.
  • INTRODUCTION: Surgical complications after tumor operations are frequent in children, with rates of up to 30% cited in the literature.
  • In a retrospective analysis, we evaluated the complications associated with tumor surgery.
  • The distribution of the various tumors, the type of surgery, and complications were evaluated.
  • RESULTS: A total of 145 operations for abdominal tumors were performed in 123 patients.
  • The three most common diseases were neuroblastoma (36%), nephroblastoma (26%), and ovarian tumor (19%).
  • In 68% of patients complete resection and in 19% of cases partial resection of the tumor was carried out; open biopsy was performed in 13%.
  • A significant increase in the risk of complications could be seen with an increase in SRFs (p=0.0267) and with disease stages 2 and 3 (p=0.016).
  • Tumor reduction surgery was also associated with an increase in complications (p=0.086).
  • CONCLUSIONS: In summary, tumor surgery is associated with considerable risks in children.
  • [MeSH-major] Abdominal Neoplasms / surgery. Imaging, Three-Dimensional. Postoperative Complications / prevention & control. Preoperative Care. Surgery, Computer-Assisted

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  • [Copyright] (c) Georg Thieme Verlag KG Stuttgart - New York.
  • (PMID = 19449285.001).
  • [ISSN] 1439-359X
  • [Journal-full-title] European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift für Kinderchirurgie
  • [ISO-abbreviation] Eur J Pediatr Surg
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] Germany
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10. Hesseling P, McCormick P, Kouya F, Soh F, Katayi T, Noglik G, Kidd M, Kenyu E, Ngam I, Tata G: Burkitt lymphoma: residual abdominal tumor volume after induction therapy correlates with outcome. Pediatr Blood Cancer; 2010 Oct;55(4):761-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Burkitt lymphoma: residual abdominal tumor volume after induction therapy correlates with outcome.
  • Staging investigations in the Malawi 2003 BL protocol included abdominal ultrasonography.
  • This sometimes demonstrated tumor that was not palpable.
  • Patients with no palpable tumor following induction with three courses of cyclophosphamide were considered to be in remission, although residual intraabdominal tumor was documented in some by chance.
  • We repeated ultrasonography on day 29 on 22 new patients with non-palpable abdominal BL following induction.
  • The relapse rate after 1 year correlated with the largest residual tumor volume, and was 17% for tumors 0-35 ml, and 75% for tumors > or = 35 ml in volume.
  • [MeSH-major] Abdominal Neoplasms / drug therapy. Burkitt Lymphoma / drug therapy
  • [MeSH-minor] Adolescent. Child. Child, Preschool. Female. Humans. Male. Neoplasm Recurrence, Local. Prospective Studies

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  • [Copyright] Copyright 2010 Wiley-Liss, Inc.
  • (PMID = 20589655.001).
  • [ISSN] 1545-5017
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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11. Bode HH, Schimana W, Swai B, Bode U: Sexual precocity associated with an abdominal tumor in an African boy. J Pediatr Endocrinol Metab; 2008 Mar;21(3):275-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Sexual precocity associated with an abdominal tumor in an African boy.
  • We report a 3 year-old boy in Tanzania with an abdominal mass and isosexual precocity due to an hCG-secreting hepatoblastoma.
  • [MeSH-major] Hepatoblastoma / pathology. Liver Neoplasms / pathology. Puberty, Precocious / etiology

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  • (PMID = 18540255.001).
  • [ISSN] 0334-018X
  • [Journal-full-title] Journal of pediatric endocrinology & metabolism : JPEM
  • [ISO-abbreviation] J. Pediatr. Endocrinol. Metab.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Chorionic Gonadotropin; 0 / alpha-Fetoproteins; 0 / beta Catenin; 6PLQ3CP4P3 / Etoposide; Q20Q21Q62J / Cisplatin
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12. Wandeler-Meyer K, Bremerich J, Christ M: [Abdominal tumor after persistent coughing and uncontrolled anticoagulation]. Praxis (Bern 1994); 2010 Jan 6;99(1):55-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Abdominal tumor after persistent coughing and uncontrolled anticoagulation].
  • [Transliterated title] Abdominaler Tumor nach anhaltendem Husten und entgleister Antikoagulation.
  • The patient presented with progressive pain in the left lower abdomen associated with a palpable mass and anaemia.
  • Abdominal sonography and computed tomography revealed a rectus sheath hematoma.
  • [MeSH-major] Abdomen, Acute / etiology. Anticoagulants / adverse effects. Atrial Fibrillation / drug therapy. Cough / complications. Hematoma / chemically induced. Intracranial Embolism / drug therapy

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  • (PMID = 20052640.001).
  • [ISSN] 1661-8157
  • [Journal-full-title] Praxis
  • [ISO-abbreviation] Praxis (Bern 1994)
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Switzerland
  • [Chemical-registry-number] 0 / Anticoagulants; A74586SNO7 / clopidogrel; OM90ZUW7M1 / Ticlopidine; Q08SIO485D / Phenprocoumon; R16CO5Y76E / Aspirin; S79O08V79F / Dalteparin
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13. Jakob J, Moesta KT, Rau B: [Increasing abdominal pain caused by abdominal tumor in a 21-year-old female]. Chirurg; 2005 Feb;76(2):175-8
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  • [Title] [Increasing abdominal pain caused by abdominal tumor in a 21-year-old female].
  • We present a case of mesenteric cystic lymphangioma in a young woman who was admitted to hospital with a history of increasing abdominal pain.
  • We discuss diagnostic means, differential diagnosis, and therapeutic management of the disease.
  • [MeSH-major] Abdominal Pain / etiology. Lymphangioma, Cystic. Mesentery. Peritoneal Neoplasms
  • [MeSH-minor] Adult. Biopsy. Diagnosis, Differential. Female. Humans. Laparoscopy. Radiography, Abdominal. Tomography, X-Ray Computed

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  • (PMID = 15551011.001).
  • [ISSN] 0009-4722
  • [Journal-full-title] Der Chirurg; Zeitschrift für alle Gebiete der operativen Medizen
  • [ISO-abbreviation] Chirurg
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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14. Spreafico F, Piva L, D'Angelo P, Terenziani M, Collini P, Gandola L, Bianchi M, Tamburini A, Provenzi M, Fossati Bellani F: Are all stage III Wilms tumors the same? Data from the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP). J Clin Oncol; 2009 May 20;27(15_suppl):10030

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Are all stage III Wilms tumors the same? Data from the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP).
  • : 10030 Background: Criteria to classifying Wilms tumor (WT) as stage III are much heterogeneous, including factors referring both to tumor biology and surgical skills.
  • Main therapy differences across the trials were the timing of abdominal radiotherapy (RT) (anticipated to 2<sup>nd</sup> week from nephrectomy) and doxorubicin cumulative dose reduction from 360 mg/m<sup>2</sup> to 240 in TW2003.
  • Reasons for stage III as follows: lymph nodes (LN) 40 cases (alone 28 cases, combined with other factors 12); cava vein tumor thrombus 7, peritoneum involvement 8, post-operative gross or microscopic tumor remains 24, pre-operative rupture 9, surgical rupture 17.
  • For 29 patients (27%) information on regional LN were missing.
  • Adjuvant therapy consisted of 8-months vincristine/dactinomycin/doxorubicin + flank 1440 cGy RT (whole abdominal 15 Gy in case of diffuse peritoneal contamination).
  • Overall 16 tumor failure occurred (2 in anaplastic tumors): abdominal relapse 8 (combined to other extra-abdominal site 3), lung 5, tumor progression 2, metacronous tumor 1.
  • Overall, RFS was 75% ±7 in patients with at least LN involvement compared to 89% ±4 in patients classified as stage III for the remaining criteria, including those without LN sampling (Logrank p.09).
  • 1440 cGy flank RT warranted satisfactory local tumor control.
  • The worse outcome reported in LN-positive patients deserves further attention.

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  • (PMID = 27962574.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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15. Santoro J, Yorke E, Rosenzweig K, Goodman K, McNamara J, Pham H, Mageras G: Abstracts. Med Phys; 2010 Jun;37(6Part12):3090-3469

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • PURPOSE: This study compares respiration-correlated kV cone beam CT (RC-kVCBCT) image guidance to standard (uncorrelated) kVCBCT for target localization in radiation treatment of thoracic and abdominal tumors.
  • METHOD AND MATERIALS: In an IRB-approved study, 9 stage II-IV non-small cell lung cancer (NSCLC) patients and 1 stage III stomach tumor patient with fiducials received a respiration-correlated planning CT (RCCT) at simulation and five RC-CBCTs during the first week of treatment.
  • The tumor in each phase of the RC-CBCT is registered to the end-expiration (EE) phase image to obtain the respiration-averaged tumor displacement relative to its EE position.
  • The RCCT and RC-CBCT images at EE are registered to obtain the tumor displacement at the EE position.
  • A vector sum of the three displacements yields the correction to the respiration-averaged tumor position.
  • CONCLUSION: Our preliminary results suggest that for many thoracic and abdominal tumors, position corrections using uncorrelated, respiration-averaged 3D imaging are consistent with those from respiration-correlated imaging; however, respiration-correlated imaging may be indicated for cases of large tumor motion.

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  • [Copyright] © 2010 American Association of Physicists in Medicine.
  • (PMID = 28512987.001).
  • [ISSN] 2473-4209
  • [Journal-full-title] Medical physics
  • [ISO-abbreviation] Med Phys
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Keywords] NOTNLM ; Cancer / Computed tomography / Cone beam computed tomography / Image reconstruction / Lungs / Medical image reconstruction / Medical imaging / Pneumodynamics / Radiation therapy / Radiation treatment
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16. de León DC, Pérez-Montiel D, Bandera A, Villegas C, Gonzalez-Conde E, Vilchis JC: Perivascular epithelioid cell tumor of abdominal origin. Ann Diagn Pathol; 2010 Jun;14(3):173-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Perivascular epithelioid cell tumor of abdominal origin.
  • Perivascular epithelioid tumor is not a common disease; therefore, large series are not available in the literature, and most are case reports.
  • Histologic characteristics of these neoplasms are positivity to melanogenic (HMB-45) and muscle stains.
  • All these neoplasms have the characteristic perivascular epithelioid cell or "PEC," but the term myomelanocyte tumor has been proposed because of the immunohistochemistry expression.
  • We report 3 cases of abdominal PEComa, 1 of them with benign clinical outcome and 2 with an aggressive behavior.
  • [MeSH-major] Epithelioid Cells / pathology. Pelvic Neoplasms / pathology. Perivascular Epithelioid Cell Neoplasms / secondary
  • [MeSH-minor] Adult. Aged. Biomarkers, Tumor / metabolism. Combined Modality Therapy. Fatal Outcome. Female. Humans. Immunohistochemistry. Tomography, X-Ray Computed

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  • (PMID = 20471562.001).
  • [ISSN] 1532-8198
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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17. Saab R, Khoury JD, Krasin M, Davidoff AM, Navid F: Desmoplastic small round cell tumor in childhood: the St. Jude Children's Research Hospital experience. Pediatr Blood Cancer; 2007 Sep;49(3):274-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Desmoplastic small round cell tumor in childhood: the St. Jude Children's Research Hospital experience.
  • BACKGROUND: Desmoplastic small round cell tumor (DSRCT) is a rare, primarily intra-abdominal tumor that has a poor outcome with current therapies.
  • PROCEDURE: We retrospectively reviewed patient characteristics, presenting symptoms, tumor pathology, treatment, and outcome of 11 pediatric patients with DSRCT at our institution.
  • In eight (73%) patients, the primary tumor was abdominal or pelvic, and in one patient each, it was submental, mediastinal, and paratesticular.
  • Nine (82%) patients had metastatic disease.
  • All tumors showed polyphenotypic differentiation by immunohistochemistry.
  • The EWS-WT1 transcript was detected in six of seven tumors tested.
  • One tumor showed rhabdomyoblastic differentiation after therapy.
  • Two died of treatment-related toxicity, six died of disease.
  • Patients with localized extra-abdominal disease have a better prognosis, most likely due to increased feasibility of resection.
  • [MeSH-major] Abdominal Neoplasms / pathology. Abdominal Neoplasms / therapy. Neoplasms, Complex and Mixed / pathology. Neoplasms, Complex and Mixed / therapy

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  • [Copyright] Copyright (c) 2006 Wiley-Liss, Inc.
  • (PMID = 16685737.001).
  • [ISSN] 1545-5009
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / CA 21765
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / EWS1-WT1 fusion protein, human; 0 / Oncogene Proteins, Fusion
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18. Yamagami Y, Ueshima S, Mizutani S, Uchikoshi F, Ohyama T, Yoshidome K, Tori M, Hiraoka K, Takahashi H, Sueyoshi K, Taira M, Kido T, Sakamaki Y, Yasukawa M, Oka K, Tsujimoto M, Nakahara M, Nakao K: [An autopsied case of giant small cell carcinoma of the pancreas]. Gan To Kagaku Ryoho; 2009 Jan;36(1):123-5
MedlinePlus Health Information. consumer health - Pancreatic Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • A 58-year-old man who complained of an abdominal tumor was admitted to our hospital.
  • Abdominal CT scan showed that a 15-cm tumor occupied the entire right upper abdomen and that there were ascites and liver metastases.
  • The liver biopsy showed a small cell carcinoma pattern, but no definitive origin of the tumor was determined.
  • Considering the extensive peritoneal invasion and multiple liver metastases, he received 2 / courses of cisplatin/etoposide chemotherapy, but his tumor became larger with concomitant abdominal pain and nausea.
  • The patient suddenly died due to multiple organ failure caused by tumor necrosis.
  • [MeSH-major] Carcinoma, Giant Cell / pathology. Carcinoma, Small Cell / pathology. Pancreatic Neoplasms / pathology
  • [MeSH-minor] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Autopsy. Fatal Outcome. Humans. Male. Middle Aged. Neoplasm Metastasis / pathology. Neoplasm Metastasis / radiography

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  • (PMID = 19151577.001).
  • [ISSN] 0385-0684
  • [Journal-full-title] Gan to kagaku ryoho. Cancer & chemotherapy
  • [ISO-abbreviation] Gan To Kagaku Ryoho
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
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19. de Lagausie P, Bonnard A, Berrebi D, Lepretre O, Statopoulos L, Delarue A, Guys JM: Abdominal lymphangiomas in children: interest of the laparoscopic approach. Surg Endosc; 2007 Jul;21(7):1153-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Abdominal lymphangiomas in children: interest of the laparoscopic approach.
  • The most common symptoms are abdominal tumor or "acute abdomen" in children.
  • CONCLUSION: The laparoscopy procedure could be used successfully for abdominal lymphangioma, even in an emergency.
  • [MeSH-major] Abdominal Neoplasms / surgery. Laparoscopy / methods. Lymphangioma / surgery
  • [MeSH-minor] Adolescent. Child. Child, Preschool. Cohort Studies. Female. Follow-Up Studies. Forecasting. Humans. Infant. Laparotomy / methods. Laparotomy / trends. Lymphangioma, Cystic / diagnosis. Lymphangioma, Cystic / surgery. Male. Minimally Invasive Surgical Procedures / methods. Minimally Invasive Surgical Procedures / trends. Neoplasm Staging. Retrospective Studies. Tomography, X-Ray Computed. Treatment Outcome. Ultrasonography, Doppler

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  • (PMID = 17177082.001).
  • [ISSN] 1432-2218
  • [Journal-full-title] Surgical endoscopy
  • [ISO-abbreviation] Surg Endosc
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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20. Tori M, Akamatsu H, Mizutani S, Yoshidome K, Oyama T, Ueshima S, Tsujimoto M, Nakahara M: Multiple benign metastasizing leiomyomas in the pelvic lymph nodes and biceps muscle: report of a case. Surg Today; 2008;38(5):432-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • A 47-year-old woman with an earlier history of uterine leiomyoma suffered from multiple recurrent tumors in the retroperitoneal lymph nodes and biceps muscle of the right upper arm.
  • The woman with a right lower abdominal tumor was referred to our hospital.
  • An abdominal computed tomography scan revealed two round nodules with well-defined margins in the retroperitoneum in the pelvis, and echography revealed a similar nodule in the biceps of the right upper arm.
  • A biopsy of the abdominal retroperitoneal tumor demonstrated benign metastasizing leiomyoma (BML).
  • An extirpation of the abdominal tumors was therefore performed.
  • [MeSH-major] Leiomyoma / pathology. Lymph Nodes / pathology. Muscle Neoplasms / pathology. Uterine Neoplasms / pathology

  • MedlinePlus Health Information. consumer health - Uterine Cancer.
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  • (PMID = 18560966.001).
  • [ISSN] 0941-1291
  • [Journal-full-title] Surgery today
  • [ISO-abbreviation] Surg. Today
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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21. Sehouli J, Senyuva F, Fotopoulou C, Neumann U, Denkert C, Werner L, Gülten OO: Intra-abdominal tumor dissemination pattern and surgical outcome in 214 patients with primary ovarian cancer. J Surg Oncol; 2009 Jun 1;99(7):424-7
MedlinePlus Health Information. consumer health - Ovarian Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Intra-abdominal tumor dissemination pattern and surgical outcome in 214 patients with primary ovarian cancer.
  • INTRODUCTION: We performed a systematic evaluation of tumor pattern and surgical outcome in 214 consecutive patients with primary ovarian cancer.
  • METHODS: Based on the surgical and histological reports we retrospectively analyzed tumor localizations, surgical and clinical outcome.
  • Cox-regression analysis was performed to identify independent predictors of complete tumor resection and mortality.
  • Upper abdominal tumor involvement was associated with a significantly higher rate of lymph node metastasis and a significantly lower rate of complete surgical tumor resection, when compared to patients with tumor limited to the lower abdomen.
  • Median overall survival was 56; 61 and 27 months for patients with tumor load in the upper, lower and whole abdomen respectively (P < 0.05).
  • CONCLUSIONS: The intraoperative tumor dissemination pattern and the post-operative tumor residuals are decisive for the prognosis in primary ovarian cancer.
  • There is an urgent need to use a systematic and standardized tumor documentation protocols to define the predictive and prognostic role of specific tumor pattern and to compare the surgical outcomes of different tumor centers.
  • [MeSH-major] Neoplasm Invasiveness. Ovarian Neoplasms / pathology. Ovarian Neoplasms / surgery
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Female. Humans. Middle Aged. Neoplasm Metastasis. Prognosis. Retrospective Studies. Survival Analysis. Treatment Outcome

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  • (PMID = 19365809.001).
  • [ISSN] 1096-9098
  • [Journal-full-title] Journal of surgical oncology
  • [ISO-abbreviation] J Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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22. Hashiguchi N, Tsuruta N, Ise S, Higuchi K: [A case of disseminated actinomycosis which extended from the thoracic cavity]. Nihon Kokyuki Gakkai Zasshi; 2010 Sep;48(9):683-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • A 74-year-old man was referred to our hospital with a high grade fever, a left abdominal tumor and bloody sputum since the beginning of April 2006.
  • We made an incision of the abdominal tumor, and the Gram-stain smear demonstrated Gram-positive rods.
  • [MeSH-minor] Abdominal Cavity / microbiology. Aged. Humans. Lung Diseases / microbiology. Male

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  • (PMID = 20954371.001).
  • [ISSN] 1343-3490
  • [Journal-full-title] Nihon Kokyūki Gakkai zasshi = the journal of the Japanese Respiratory Society
  • [ISO-abbreviation] Nihon Kokyuki Gakkai Zasshi
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
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23. Halpin VJ, Underwood RA, Ye D, Cooper DH, Wright M, Hickerson SM, Connett WC, Connett JM, Fleshman JW: Pneumoperitoneum does not influence trocar site implantation during tumor manipulation in a solid tumor model. Surg Endosc; 2005 Dec;19(12):1636-40
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Pneumoperitoneum does not influence trocar site implantation during tumor manipulation in a solid tumor model.
  • BACKGROUND: The purpose of this study was to assess tumor implantation at abdominal wound sites following manipulation of a solid abdominal tumor.
  • At 2 weeks, an omental tumor was harvested and animals were randomized to bivalve (A), crush (B), strip (C), or excision (D), with or without pneumoperitoneum.
  • Four 5-mm trocars were inserted into the abdomen, and the tumor was reinserted through the midline, swept through four quadrants, and removed.
  • Tumor implantation at wound sites was documented at 7 weeks.
  • CONCLUSIONS: Tumor implantation at trocar sites is due to spillage of tumor during manipulation and not to pneumoperitoneum.
  • [MeSH-major] Colonic Neoplasms / secondary. Colonic Neoplasms / surgery. Laparoscopy / adverse effects. Neoplasm Seeding. Pneumoperitoneum, Artificial / adverse effects
  • [MeSH-minor] Animals. Cell Line, Tumor. Cricetinae. Humans. Laparoscopes. Male. Mesocricetus. Neoplasm Transplantation

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  • (PMID = 16211435.001).
  • [ISSN] 1432-2218
  • [Journal-full-title] Surgical endoscopy
  • [ISO-abbreviation] Surg Endosc
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
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24. Louzi A, Rifki SE, Benamar Y, Attari M, Kafih M, Zerouali NO: [Colonic actinomycosis: report of a case and review of the literature]. Ann Chir; 2005 Feb;130(2):101-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Transliterated title] Actinomycose colique: à propos d'un cas et revue de la littérature.
  • Abdominal localizations are rare and simulated a malignant process.
  • We report a colonic actinomycosis case of a 62-year-old woman with a abdominal tumor and diagnosed after surgical resection.
  • [MeSH-minor] Colonic Neoplasms / diagnosis. Diagnosis, Differential. Diagnostic Errors. Female. Humans. Middle Aged

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  • (PMID = 15737322.001).
  • [ISSN] 0003-3944
  • [Journal-full-title] Annales de chirurgie
  • [ISO-abbreviation] Ann Chir
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] France
  • [Number-of-references] 17
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25. Yoshimura N, Ohara H, Miyabe K, Ban T, Sano H, Naitoh I, Hayashi K, Ando T, Nakazawa T, Joh T: A case of gastrointestinal stromal tumor with spontaneous rupture in the greater omentum. Int Semin Surg Oncol; 2008;5:19

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A case of gastrointestinal stromal tumor with spontaneous rupture in the greater omentum.
  • BACKGROUND: Although GIST generally occurs in the digestive tract, such as the stomach, and small and small intestine primarily, Omental GIST tumours are very rare.
  • CASE PRESENTATION: A 63-year-old male patient, who recognized an abdominal tumor 1 year before admission, had a slight expansion of the tumor, reduction of the body and malaise, was consulted to our hospital.
  • Abdominal CT and MRI revealed a cystic lesion of 26 cm in diameter with a clear boundary from immediately below the interseptum to the pelvic cavity, and imaged the septum and cystic wall.
  • We considered that the patient had a cystic tumor in the abdomen, of which the primary lesion was unknown, and scheduled surgery.
  • The patient unfortunately deteriorated with shock and sudden pain in the abdomen.
  • Wediagnosed tumor rapture, and emergency surgery was performed.
  • The tumor, weighing 3,600 g, was mostly cystic, and filled with sanguinous fluid and clot.
  • Histologically, the tumor was composed of spindle cells, and was positive for c-KIT (CD117), slightly positive for alpha-smooth muscle actin (SMA), and S-100 protein positive.
  • Based on these findings, the tumor was diagnosed as GIST primarily occurring in the greater omentum.

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  • [Cites] Am J Surg Pathol. 1999 Sep;23(9):1109-18 [10478672.001]
  • [Cites] Ann Surg. 2000 Jan;231(1):51-8 [10636102.001]
  • [Cites] Pathol Int. 2001 Jul;51(7):524-31 [11472565.001]
  • [Cites] Science. 1998 Jan 23;279(5350):577-80 [9438854.001]
  • (PMID = 18664259.001).
  • [ISSN] 1477-7800
  • [Journal-full-title] International seminars in surgical oncology : ISSO
  • [ISO-abbreviation] Int Semin Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2515846
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26. Saredi G, Di Pietro C, Spasciani R, De Stefani S, Sighinolfi MC, Micali S, Bianchi G: Tumor seeding after open nephroureterectomy for ureteral transitional cell carcinoma. Tumori; 2008 Jul-Aug;94(4):600-1
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  • [Title] Tumor seeding after open nephroureterectomy for ureteral transitional cell carcinoma.
  • Few cases of abdominal wall metastasis have been reported in the literature and attributed to tumor seeding after laparoscopic surgery or percutaneous nephrostomy.
  • We report a case of abdominal tumor seeding after open nephroureterectomy managed by means of a surgical and medical approach.
  • [MeSH-major] Abdominal Neoplasms / etiology. Carcinoma, Transitional Cell / surgery. Neoplasm Seeding. Ureteral Neoplasms / surgery. Urologic Surgical Procedures / adverse effects

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  • (PMID = 18822702.001).
  • [ISSN] 0300-8916
  • [Journal-full-title] Tumori
  • [ISO-abbreviation] Tumori
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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27. Barreda Bolaños F, Liu Bejarano H, Sánchez Lihon J, Landeo Aliaga I, Sánchez Rodríguez Z: [Survival factors in 152 patients with gastrointestinal stromal tumors]. Rev Gastroenterol Peru; 2010 Oct-Dec;30(4):305-23
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Survival factors in 152 patients with gastrointestinal stromal tumors].
  • [Transliterated title] Factores de sobrevida en 152 pacientes con tumores estromales gastrointestinales.
  • INTRODUCTION: The gastrointestinal stromal tumor (GIST) is the designation for a specific type of mesenchymal tumor of the digestive tract that is origin in the interstitial cells of Cajal (ICC) or its precursor multipotentials, its presentation is rare and therefore its best knowledge must affect a proper diagnosis and treatment.
  • OBJECTIVES: To evaluate the clinical characteristics and to identify factors influencing survival of patients with gastrointestinal stromal tumor.
  • The study has been performed in 152 patients with gastrointestinal stromal tumor who were treated at the National Institute of Neoplastic Diseases (INEN), Lima, Peru, from January 1999 through December 2009.
  • The initial presentation was with localized disease to 79 patients (52%) and primary metastases in 73 patients (48%), with an average time of disease 14 months.
  • The prevalence of GIST tumor in the different organs was as follows: stomach with 77 patients (50.65%), jejunum with 21 patients (13.82%), retroperitoneum with 17 patients (11.18%), duodenum 11 patients (7.24%), colon 11 patients (7.24%), ileum 8 patients (5.26%),pancreas, 3 patients (1.97%), rectum, 3 patients (1.97%) and esophagus with 1 patient (0.66%).
  • The most common symptoms of GIST tumors in general were gastrointestinal bleeding, abdominal tumor and abdominal pain.
  • The tumor size greater than 10 centimeters was found in 92 patients (60.51%), 39 patients had size between 5 and 10 centimeters (25.65%) and 20 patients had lesions smaller than 5 centimeters (13.15%).
  • Retroperitoneal GIST tumors had an expression of CD117 of 92.86% and CD34 of 60%, and GIST tumors of the pancreas had an expression of CD117 of 100% and CD34 of 100%.
  • Of the 152 patients, 93 had complete resection of the disease, 28 had partial resection, 24 were unresectable and 07 did not undergo surgery, the more aggressive behavior was observed in ileum, 03 patients were unresectable, 02 patients had partial resection and only 02 could be completely resected, the rest of the series in general, for each location, the GIST tumors completely resected outscored the unresectable and partially resected.
  • The survival of patients under and over 50 expressed a p = 0.08, cumulative survival rates by tumor size expressed p = 0.56, cumulative survival rates for stomach and intestinal location shows a p = 0.056.
  • Multivariate analysis showed that the most significant factor for disease progression was the primary metastases with p = 0.007, and that survival was directly related to complete resection of the disease which is expressed with p <0.0001.
  • CONCLUSIONS: The most important prognostic factor of survival for gastrointestinal stromal tumors (GIST) is the complete resection of the disease.
  • The factor that is associated with progression of the disease is the presence of metastases.
  • In our series of 152 patients, tumor locations tend to relate better survival in gastric GIST that in intestinal GIST.
  • Differentiated tumor size in three size categories expressed no more related to survival.
  • The low mitotic index associated with metastasis, not reflected a good prognosis of disease.
  • [MeSH-major] Gastrointestinal Stromal Tumors / mortality

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  • (PMID = 21263758.001).
  • [ISSN] 1022-5129
  • [Journal-full-title] Revista de gastroenterología del Perú : órgano oficial de la Sociedad de Gastroenterología del Perú
  • [ISO-abbreviation] Rev Gastroenterol Peru
  • [Language] spa
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Peru
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28. Oosterling SJ, van der Bij GJ, Bögels M, van der Sijp JR, Beelen RH, Meijer S, van Egmond M: Insufficient ability of omental milky spots to prevent peritoneal tumor outgrowth supports omentectomy in minimal residual disease. Cancer Immunol Immunother; 2006 Sep;55(9):1043-51

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Insufficient ability of omental milky spots to prevent peritoneal tumor outgrowth supports omentectomy in minimal residual disease.
  • BACKGROUND: The greater omentum is frequently involved in the course of gastrointestinal and ovarian tumors.
  • Paradoxically, many immune cells, such as macrophages that accumulate in so-called milky spots, reside within the omentum and are cytotoxic against tumor cells ex vivo.
  • Consequently, omental macrophages might play an important role in killing tumor cells, and may hereby prevent development into local peritoneal recurrences.
  • In the present study, we therefore evaluated the role of the omentum and the clinical relevance of omentectomy in minimal residual disease (MRD).
  • METHODS: Tumor cell dissemination patterns on the omentum in a rat model were examined using DiI-labelled CC531s tumor cells.
  • Additionally, intra peritoneal (i.p.) tumor load was investigated in rats that underwent omentectomy or sham laparotomy followed by i.p. injection of CC531s cells on day 21, which represented MRD.
  • RESULTS: At 4 h post injection, tumor cells predominantly adhered on milky spots.
  • Number of cells thereafter declined rapidly suggesting initial tumor killing functions in these specific immune aggregates.
  • Despite initial reduction observed in milky spots, numbers of tumor cells however increased at fatty tissue stripes that border the omentum.
  • This indicated proliferation at these locations, which corresponded to macroscopic observations of the omenta on day 21 after tumor cell injection.
  • Omentectomy resulted in reduced intra-abdominal tumor load, which was completely attributable to the absence of the omentum, as tumor development did not differ on other sites.
  • Even in the MRD group microscopic clusters of tumor cells located in the omentum eventually developed into macroscopic nodules.
  • CONCLUSION: Since the ability of omental milky spots is, even in MRD, insufficient to prevent intra abdominal tumor outgrowth, omentectomy, which reduces tumor load, is recommended in surgical treatment of intra abdominal tumors that are prone to disseminate intraperitoneally.
  • [MeSH-major] Adenocarcinoma / prevention & control. Colonic Neoplasms / prevention & control. Omentum / pathology. Omentum / surgery. Peritoneal Neoplasms / prevention & control
  • [MeSH-minor] Adipose Tissue / pathology. Animals. Cell Adhesion / immunology. Cell Line, Tumor. Cell Proliferation. Digestive System Surgical Procedures. Disease Models, Animal. Lymphoid Tissue / pathology. Macrophages / immunology. Male. Neoplasm Transplantation. Neoplasm, Residual. Rats

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  • (PMID = 16311732.001).
  • [ISSN] 0340-7004
  • [Journal-full-title] Cancer immunology, immunotherapy : CII
  • [ISO-abbreviation] Cancer Immunol. Immunother.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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29. Hayashi M, Asakuma M, Tsunemi S, Inoue Y, Shimizu T, Komeda K, Hirokawa F, Takeshita A, Egashira Y, Tanigawa N: Surgical treatment for abdominal actinomycosis: A report of two cases. World J Gastrointest Surg; 2010 Dec 27;2(12):405-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Surgical treatment for abdominal actinomycosis: A report of two cases.
  • Since actinomycosis sometimes causes an abdominal tumor which mimics malignancy, treatment strategy varies from case to case.
  • Both patients presented with an intra-abdominal tumor lesion mimicking malignant disease after an appendectomy for acute appendicitis.
  • Case 1 received surgical extirpation of the abdominal tumor in the liver and kidney twice since the clinical diagnosis of actinomycosis was not made.

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  • [Cites] Clin Microbiol Infect. 2003 Aug;9(8):881-5 [14616714.001]
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  • (PMID = 21206723.001).
  • [ISSN] 1948-9366
  • [Journal-full-title] World journal of gastrointestinal surgery
  • [ISO-abbreviation] World J Gastrointest Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] China
  • [Other-IDs] NLM/ PMC3014523
  • [Keywords] NOTNLM ; Abdominal actinomycosis / Laparoscopic surgery / Single port surgery / Surgical therapy
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30. Katz DS, Yam B, Hines JJ, Mazzie JP, Lane MJ, Abbas MA: Uncommon and unusual gastrointestinal causes of the acute abdomen: computed tomographic diagnosis. Semin Ultrasound CT MR; 2008 Oct;29(5):386-98
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Uncommon and unusual gastrointestinal causes of the acute abdomen: computed tomographic diagnosis.
  • There is a wide variety of uncommon and unusual gastrointestinal causes of acute abdominal and pelvic pain that may be prospectively diagnosed on computed tomography.
  • We demonstrate 10 such diagnoses and briefly review the current computed tomography and clinical literature on intussusception occurring beyond early childhood, small bowel obstruction from internal hernia, cecal volvulus, intramural small bowel hemorrhage, Boerhaave's syndrome, gastrointestinal luminal foreign bodies, small bowel diverticulitis, hemoperitoneum secondary to abdominal tumor; gallstone ileus, and gallbladder torsion.
  • Radiologists and clinicians need to be aware of these disorders, particularly with the widespread utilization of computed tomography (CT) in the management of patients with acute abdominal pain.
  • [MeSH-major] Abdomen, Acute / diagnosis. Abdomen, Acute / etiology. Gastrointestinal Diseases / complications. Gastrointestinal Diseases / radiography. Radiography, Abdominal / methods. Tomography, X-Ray Computed / methods

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  • (PMID = 18853844.001).
  • [ISSN] 0887-2171
  • [Journal-full-title] Seminars in ultrasound, CT, and MR
  • [ISO-abbreviation] Semin. Ultrasound CT MR
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 55
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31. Okumura F, Senoo K, Yoshida M, Miyabe K, Naito I, Tanaka H, Hayashi K, Ando T, Nakazawa T, Ohara H, Hamaguchi K, Kanai M, Ito K, Joh T: [A case of peritoneal dissemination from mucinous carcinoma of the duodenum, which was associated with tumor thrombosis in the accessory pancreatic duct and successfully treated by chemotherapy]. Nihon Shokakibyo Gakkai Zasshi; 2009 Dec;106(12):1736-43
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [A case of peritoneal dissemination from mucinous carcinoma of the duodenum, which was associated with tumor thrombosis in the accessory pancreatic duct and successfully treated by chemotherapy].
  • A 72-year-old woman was admitted with an abdominal tumor, which had been detected by computed tomography scanning.
  • Endoscopic examination of the upper gastrointestinal tract revealed a type 3 tumor in the descending limb of the duodenum.
  • The pathological findings indicated primary duodenal cancer (mucinous carcinoma) associated with tumor thrombosis in the accessory pancreatic duct.
  • [MeSH-major] Adenocarcinoma, Mucinous / pathology. Duodenal Neoplasms / pathology. Neoplastic Cells, Circulating / pathology. Pancreatic Ducts / pathology. Peritoneal Neoplasms / secondary

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  • (PMID = 19966515.001).
  • [ISSN] 0446-6586
  • [Journal-full-title] Nihon Shokakibyo Gakkai zasshi = The Japanese journal of gastro-enterology
  • [ISO-abbreviation] Nihon Shokakibyo Gakkai Zasshi
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Japan
  • [Number-of-references] 30
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32. de la Fuente-Lira M, Rocha-Guevara ER, Márquez-Rocha ML, Salazar-Lozano C, Jaramillo-Solís O, Ortiz-Maldonado AL: [Appendiceal mucocele and gangrenous cholecystitis]. Cir Cir; 2006 Jul-Aug;74(4):273-7
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  • SETTING: Hospital de Especialidades, Centro Médico Nacional Siglo XXI, México, D.F.
  • CLINICAL CASE: An 80-year-old man was admitted to the hospital with diagnosis of acute cholecystitis and abdominal tumor under study, with complaints of abdominal pain for 10 days located in the right upper quadrant, without fever or significant weight loss.
  • CT of the abdomen revealed thickening of the gallbladder wall and acute local inflammation, as well as the presence of abdominal tumor in the right lower quadrant.
  • The patient was surgically explored with the following findings: gangrenous cholecystitis and appendiceal tumor of 20 cm length.

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  • (PMID = 17022900.001).
  • [ISSN] 0009-7411
  • [Journal-full-title] Cirugía y cirujanos
  • [ISO-abbreviation] Cir Cir
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Mexico
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33. Machimoto T, Doi R, Ogawa K, Masui T, Seo S, Uemoto S: Abdominal wall recurrence of Hilar bile duct cancer 12 years after a curative resection: report of a case. Surg Today; 2009;39(1):72-6
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  • [Title] Abdominal wall recurrence of Hilar bile duct cancer 12 years after a curative resection: report of a case.
  • Ten years later (April 2005), she noted a small mass in the abdominal wall.
  • The abdominal wall tumor was buried in the rectus abdominis muscle and was tightly attached to the ileum.
  • In addition, the immunohistochemical staining pattern of the abdominal tumor was identical to that of the original bile duct cancer.
  • This indicated that the abdominal tumor represented a local recurrence (probably due to peritoneal implantation) at 12 years after the resection of the hilar bile duct cancer.
  • [MeSH-major] Abdominal Neoplasms / pathology. Adenocarcinoma / pathology. Bile Duct Neoplasms / pathology. Bile Ducts / pathology. Neoplasms, Second Primary / pathology
  • [MeSH-minor] Abdominal Wall. Aged. Female. Hepatectomy / methods. Humans. Immunohistochemistry. Prognosis. Recurrence. Treatment Outcome

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  • (PMID = 19132474.001).
  • [ISSN] 0941-1291
  • [Journal-full-title] Surgery today
  • [ISO-abbreviation] Surg. Today
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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34. Gomes AL, Freitas Filho LG, Leão JQ, Heinisch AC, Carnevale J: Ectopic opening of the vas deferens into a Müllerian duct cyst. J Pediatr Urol; 2007 Apr;3(2):151-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Ectopic opening of the vas deferens into Müllerian duct cysts is a rare entity but should always be considered when a child presents with purulent urinary discharge and abdominal tumor.

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  • (PMID = 18947723.001).
  • [ISSN] 1873-4898
  • [Journal-full-title] Journal of pediatric urology
  • [ISO-abbreviation] J Pediatr Urol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
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35. Fujiu K, Sakuma H, Shio Y, Suzuki H, Mori M: [A case of non-Hodgkin's lymphoma after chemotherapy for cancer of unknown origin]. Gan To Kagaku Ryoho; 2008 Nov;35(11):1907-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Computed tomography(CT)scans showed a swelling of the superior mediastinal lymph node and a tumor of the right lobe of thyroid gland.
  • Seven months later, CT and positron emission tomography revealed swelling of the mediastinal lymph nodes and a tumor in the left abdominal tumor.
  • An open biopsy of the abdominal tumor demonstrated non-Hodgkin's lymphoma, mature B cell type, follicular lymphoma, grade 1.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Lymphoma, Non-Hodgkin / drug therapy. Lymphoma, Non-Hodgkin / pathology. Neoplasms, Unknown Primary / drug therapy. Neoplasms, Unknown Primary / pathology
  • [MeSH-minor] Aged. Biomarkers, Tumor / blood. Biopsy. Carcinoma, Adenosquamous / drug therapy. Carcinoma, Adenosquamous / pathology. Carcinoma, Adenosquamous / radiography. Carcinoma, Adenosquamous / surgery. Combined Modality Therapy. Humans. Male. Tomography, X-Ray Computed. Treatment Failure

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  • (PMID = 19011340.001).
  • [ISSN] 0385-0684
  • [Journal-full-title] Gan to kagaku ryoho. Cancer & chemotherapy
  • [ISO-abbreviation] Gan To Kagaku Ryoho
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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36. An JY, Heo JS, Noh JH, Sohn TS, Nam SJ, Choi SH, Joh JW, Kim SJ: Primary malignant retroperitoneal tumors: analysis of a single institutional experience. Eur J Surg Oncol; 2007 Apr;33(3):376-82

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary malignant retroperitoneal tumors: analysis of a single institutional experience.
  • AIMS: In order to achieve complete resection in the surgical management of retroperitoneal tumors, it is crucial to know the tumor's anatomical location relative to neighboring organs.
  • METHODS: Forty-nine patients with primary malignant retroperitoneal tumors were divided by tumor location into two groups [upper abdomen (group 1) or lower abdomen (group 2)], and clinicopathological features, tumor recurrence, and patient survival were assessed.
  • RESULTS: No significant differences in preoperative clinical characteristics existed between two groups, and liposarcoma was the most frequently observed tumor type.
  • The 5-year survival rate of patients with tumors smaller than 10 cm was 78.4%, while that of patients with tumors larger than 10 cm was 38.1% (p=0.017).
  • CONCLUSIONS: An upper abdominal tumor location is a positive prognostic factor even if small tumor size (<10 cm) and complete resection of the tumor are still more important factors to improve outcome in patients with malignant primary retroperitoneal tumors.
  • Because complete resection was shown to be the most important prognostic factor, an aggressive and careful surgical approach is recommended for the treatment of such tumors.
  • [MeSH-major] Liposarcoma / surgery. Retroperitoneal Neoplasms / surgery
  • [MeSH-minor] Adolescent. Adult. Aged. Chi-Square Distribution. Female. Humans. Male. Middle Aged. Neoplasm Recurrence, Local. Proportional Hazards Models. Survival Rate. Treatment Outcome

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  • (PMID = 17129700.001).
  • [ISSN] 0748-7983
  • [Journal-full-title] European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology
  • [ISO-abbreviation] Eur J Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
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37. Georgin-Lavialle S, Aouba A, Canioni D, Rieux-Laucat F, Fischer A, Hermine O: Accessory spleen: differential diagnosis for lymphoma in autoimmune lymphoproliferative syndrome. Pediatr Blood Cancer; 2010 Jul 1;54(7):1020-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Mutations of Fas or, less frequently, Fas ligand genes result in a rare inherited lymphoid disorder called autoimmune lymphoproliferative syndrome (ALPS) in which lymphoma frequency is increased.
  • We report on a patient with ALPS who had been splenectomized for giant splenomegaly and progressively developed a voluminous abdominal tumor.
  • The histology of the removed tumor revealed that it was an accessory spleen exhibiting typical features of ALPS involvement, as shown by the presence of a large excess of CD3+CD4-CD8- T cells and plasma cells without a detectable monoclonal population.
  • [MeSH-major] Abdomen / pathology. Autoimmune Lymphoproliferative Syndrome / complications. Choristoma / pathology. Lymphoma / pathology. Spleen

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  • [Copyright] Copyright 2010 Wiley-Liss, Inc.
  • (PMID = 20162683.001).
  • [ISSN] 1545-5017
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD95
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38. Tica VI, Beghim M, Beghim E, Dehelean I, Zaher M, Tica I: [Urachal cyst in an adult woman]. Chirurgia (Bucur); 2007 Mar-Apr;102(2):227-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Transliterated title] Chist voluminos de uracă la o femeie adultă.
  • We report a case of urachal cyst in an adult woman in whom it was difficult to determine preoperatively the origin of the abdominal tumor.
  • Even rare, this pathology should be considered in the differential diagnosis of an abdominal cyst.

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  • (PMID = 17615928.001).
  • [ISSN] 1221-9118
  • [Journal-full-title] Chirurgia (Bucharest, Romania : 1990)
  • [ISO-abbreviation] Chirurgia (Bucur)
  • [Language] rum
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Romania
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39. Hunold A, Alzen G, Wudy SA, Bluetters-Sawatzki R, Landmann E, Reiter A, Wagner HJ: Ovarian tumor in a 12-year old female with severe hypothyroidism: A case of Van Wyk and Grumbach syndrome. Pediatr Blood Cancer; 2009 May;52(5):677-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Ovarian tumor in a 12-year old female with severe hypothyroidism: A case of Van Wyk and Grumbach syndrome.
  • We report a 12-year-old female presenting with an abdominal tumor.
  • We refrained from ovariectomy, which would be necessary for a malignant tumor, in view of an evident Van Wyk and Grumbach syndrome.
  • [MeSH-major] Hypothyroidism / complications. Hypothyroidism / pathology. Ovarian Cysts / complications. Ovarian Cysts / pathology. Ovarian Neoplasms / complications. Ovarian Neoplasms / pathology

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  • [Copyright] (c) 2009 Wiley-Liss, Inc.
  • (PMID = 19127572.001).
  • [ISSN] 1545-5017
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] Q51BO43MG4 / Thyroxine
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40. Sasaki Y, Niwa Y, Ando N, Otsuka Y, Ohmiya N, Hirooka Y, Itoh A, Furuta S, Goto H: Efficacy of STI571 for a patient with metastatic gastrointestinal stromal tumor. Hepatogastroenterology; 2005 Nov-Dec;52(66):1764-7
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  • [Title] Efficacy of STI571 for a patient with metastatic gastrointestinal stromal tumor.
  • A 65-year-old man was referred to our hospital for evaluation of his huge abdominal tumor.
  • He was diagnosed as having a gastrointestinal stromal tumor arising from the stomach.
  • The tumors shrank and serum lactate dehydrogenase and alkaline phosphatase concentrations fell to below the normal limit three months later.
  • STI571 was effective medicine for the metastatic gastrointestinal stromal tumor for six months in this case.
  • [MeSH-major] Gastrointestinal Neoplasms / drug therapy. Gastrointestinal Neoplasms / pathology. Gastrointestinal Stromal Tumors / drug therapy. Gastrointestinal Stromal Tumors / pathology. Palliative Care. Piperazines / administration & dosage. Pyrimidines / administration & dosage
  • [MeSH-minor] Aged. Benzamides. Biopsy, Needle. Disease Progression. Dose-Response Relationship, Drug. Drug Administration Schedule. Fatal Outcome. Humans. Imatinib Mesylate. Immunohistochemistry. Male. Neoplasm Staging. Risk Assessment. Time Factors. Tomography, X-Ray Computed

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  • (PMID = 16334774.001).
  • [ISSN] 0172-6390
  • [Journal-full-title] Hepato-gastroenterology
  • [ISO-abbreviation] Hepatogastroenterology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Greece
  • [Chemical-registry-number] 0 / Benzamides; 0 / Piperazines; 0 / Pyrimidines; 8A1O1M485B / Imatinib Mesylate
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41. Jung B, Påhlman L, Johansson R, Nilsson E: Rectal cancer treatment and outcome in the elderly: an audit based on the Swedish Rectal Cancer Registry 1995-2004. BMC Cancer; 2009;9:68
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  • Patients > or = 75 years were less likely to have distant metastases than younger patients (14.8% vs. 17.8%, P < 0.001), and underwent abdominal tumor resection less frequently (68.5% vs. 84.4%, P < 0.001).
  • Of 11,725 patients with abdominal tumor resection (anterior resection [AR], abdominoperineal excision [APE], and Hartmann's procedure [HA]), 37.4% were > or = 75 years.
  • Choice of abdominal operation differed significantly between the two age groups for both curative and non-curative surgery, The frequency of APE was similar in both age groups (29.5% vs. 28.6%), but patients > or = 75 years were more likely to have HA (16.9% vs. 4.9%) and less likely to have preoperative radiotherapy (34.3 vs. 67.2%, P < 0.001).
  • Local recurrence following surgery for low tumors and quality of life aspects deserve particular attention.
  • [MeSH-major] Rectal Neoplasms / radiotherapy. Rectal Neoplasms / surgery
  • [MeSH-minor] Age Factors. Aged. Aged, 80 and over. Combined Modality Therapy. Digestive System Surgical Procedures / methods. Female. Humans. Male. Medical Audit. Neoplasm Recurrence, Local / pathology. Neoplasm Staging. Registries. Survival Rate. Sweden

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  • (PMID = 19245701.001).
  • [ISSN] 1471-2407
  • [Journal-full-title] BMC cancer
  • [ISO-abbreviation] BMC Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2653041
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42. Bonnet S, Durand X, Baton O, Gimenez-Roqueplo AP, Baudin E, Visset J, Algayres JP, Baranger B: [Malignant hereditary paraganglioma: problems raised by non-functional forms management]. Ann Chir; 2006 Dec;131(10):626-30

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Transliterated title] Paragangliomes malins héréditaires: problèmes liés à la prise en charge des formes non sécrétantes.
  • Non-functional paraganglioma have not clinical or biological characteristics, so that the diagnostic is most of the time delayed and made on the occasion of advanced abdominal tumor or symptomatic metastasis management.
  • [MeSH-major] Abdominal Neoplasms / genetics. Paraganglioma / genetics
  • [MeSH-minor] Adult. Base Sequence / genetics. Exons / genetics. Female. Humans. Iron-Sulfur Proteins / genetics. Mutation / genetics. Omentum / pathology. Peritoneal Neoplasms / genetics. Sequence Deletion / genetics. Succinate Dehydrogenase / genetics

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  • (PMID = 16815237.001).
  • [ISSN] 0003-3944
  • [Journal-full-title] Annales de chirurgie
  • [ISO-abbreviation] Ann Chir
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Iron-Sulfur Proteins; EC 1.3.5.1 / SDHB protein, human; EC 1.3.99.1 / Succinate Dehydrogenase
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43. Izumi H, Dowaki S, Matsuyama M, Yazawa N, Tobita K, Imaizumi T, Makuuchi H: [Retroperitoneal liposarcoma: a case report]. Nihon Shokakibyo Gakkai Zasshi; 2010 Sep;107(9):1505-12
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  • A 35-year-old woman who had visited an other hospital because of epigastralgia and anorexia was found to have a giant abdominal tumor, and was referred to our hospital.
  • On admission, the abdomen was markedly distended.
  • Abdominal CT scan and MRI showed the presence of a retroperitoneal tumor which occupied almost the entire abdominal cavity.
  • The tumor was located between the subphrenic space and the pelvic cavity, and was compressing the stomach, duodenum, pancreas and colon.
  • Removal of the retroperitoneal tumor, including the right kidney, was performed.
  • The resected tumor was 34 × 28 × 20 cm, weighed 5.5 kg and showed a variety of finding.
  • [MeSH-major] Liposarcoma / pathology. Retroperitoneal Neoplasms / pathology

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  • (PMID = 20827048.001).
  • [ISSN] 0446-6586
  • [Journal-full-title] Nihon Shokakibyo Gakkai zasshi = The Japanese journal of gastro-enterology
  • [ISO-abbreviation] Nihon Shokakibyo Gakkai Zasshi
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Japan
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44. Kobayashi M, Okamoto K, Nakatani H, Okabayashi T, Namikawa T, Ichikawa K, Kitagawa H, Araki K: Complete remission of recurrent gastrointestinal stromal tumors after treatment with imatinib: report of a case. Surg Today; 2006;36(8):727-32
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  • [Title] Complete remission of recurrent gastrointestinal stromal tumors after treatment with imatinib: report of a case.
  • A 49-year-old man underwent partial resection of the jejunum for an abdominal tumor, which was histologically confirmed to be a gastrointestinal stromal tumor (GIST).
  • Immunohistochemistry revealed that the tumor cells were positive for c-kit, p52, and MIB-1.
  • He underwent resection of a total of 83 recurrent tumors over the next 36 months.
  • A computed tomography (CT) scan done a few months later showed multiple tumor recurrences.
  • The patient was started on imatinib mesylate 400 mg/day, and 3 months later, a CT image showed an increase in tumor size but a decrease in tumor density.
  • Subsequent CT scans showed a marked decrease in tumor size 3 months later and no evidence of tumor recurrence 9 and 12 months after the commencement of imatinib treatment.
  • [MeSH-major] Antineoplastic Agents / therapeutic use. Gastrointestinal Stromal Tumors / drug therapy. Piperazines / therapeutic use. Protein Kinase Inhibitors / therapeutic use. Protein-Tyrosine Kinases / antagonists & inhibitors. Pyrimidines / therapeutic use

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  • (PMID = 16865518.001).
  • [ISSN] 0941-1291
  • [Journal-full-title] Surgery today
  • [ISO-abbreviation] Surg. Today
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Benzamides; 0 / Piperazines; 0 / Protein Kinase Inhibitors; 0 / Pyrimidines; 8A1O1M485B / Imatinib Mesylate; EC 2.7.10.1 / Protein-Tyrosine Kinases
  • [Number-of-references] 29
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45. Zhou XM, Shao SJ, Xu GD, Zhong RT, Liu DY, Tang JW, Gao YN, Cheng SJ, Lin BC: Highly sensitive determination of the methylated p16 gene in cancer patients by microchip electrophoresis. J Chromatogr B Analyt Technol Biomed Life Sci; 2005 Feb 25;816(1-2):145-51

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The p16 tumor suppressor gene is inactivated by promoter region hypermethylation in many types of tumor.
  • Recent studies showed that aberrant methylation of the p16 gene is an early event in many tumors, especially in lung cancer, and may constitute a new biomarker for early detection and monitoring of prevention trials.
  • We detected tumor-associated aberrant hypermethylation of the p16 gene in plasma and tissue DNA from 153 specimens using a modified semi-nested methylation-specific PCR (MSP) combining plastic microchip electrophoresis or slab gel electrophoresis, respectively.
  • Specimens were from 79 lung cancer patients, 15 abdominal tumor patients, 30 positive controls and 30 negative controls.
  • [MeSH-major] DNA Methylation. Electrophoresis, Microchip / methods. Genes, p16. Neoplasms / genetics
  • [MeSH-minor] Abdominal Neoplasms / blood. Abdominal Neoplasms / genetics. Feasibility Studies. Humans. Lung Neoplasms / blood. Lung Neoplasms / genetics. Polymethyl Methacrylate. Sensitivity and Specificity

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  • (PMID = 15664344.001).
  • [ISSN] 1570-0232
  • [Journal-full-title] Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
  • [ISO-abbreviation] J. Chromatogr. B Analyt. Technol. Biomed. Life Sci.
  • [Language] eng
  • [Publication-type] Comparative Study; Evaluation Studies; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 9011-14-7 / Polymethyl Methacrylate
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46. Kilic D, Findikcioglu A, Sahin E, Bilen A, Bakiner O, Hatipoglu A: Bilateral trapped lung with concomitant Wermer's syndrome and cutis laxa. Thorac Cardiovasc Surg; 2008 Dec;56(8):496-7
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  • Additional investigation revealed adenoma of the parathyroid and hypophysis, a neuroendocrine abdominal tumor, and cutis laxa.
  • [MeSH-major] Cutis Laxa / complications. Lung / pathology. Multiple Endocrine Neoplasia Type 1 / complications

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  • (PMID = 19012220.001).
  • [ISSN] 0171-6425
  • [Journal-full-title] The Thoracic and cardiovascular surgeon
  • [ISO-abbreviation] Thorac Cardiovasc Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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47. Feussner H, Härtl F: [Staging laparoscopy in oncology]. Chirurg; 2006 Nov;77(11):971-80
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  • Visual exploration of the abdominal cavity in extended diagnostic laparoscopy (EDL), including surgical dissection of areas which are primarily inaccessible, biopsy retrieval, and laparoscopic ultrasound, is superior in the diagnostic workup of early peritoneal carcinomatosis and (small) liver metastases.
  • In esophageal carcinoma, pretherapeutic EDL is valuable in case of advanced adenocarcinoma of the distal esophagus (AEG I according to Siewert), whereas the incidence of abdominal tumor manifestations in squamous cell carcinoma is too low to perform staging laparoscopy.
  • [MeSH-major] Biopsy / instrumentation. Digestive System Neoplasms / pathology. Laparoscopes. Neoplasm Staging

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  • (PMID = 17066269.001).
  • [ISSN] 0009-4722
  • [Journal-full-title] Der Chirurg; Zeitschrift für alle Gebiete der operativen Medizen
  • [ISO-abbreviation] Chirurg
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 91
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48. Yang HJ, Kim TH, Park MK, Lim CH, Lee KH, Kim CW, Han SW, Kim JA: [A case of primary extragastrointestinal stromal tumor presenting as peritoneal dissemination]. Korean J Gastroenterol; 2010 Nov;56(5):319-23

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [A case of primary extragastrointestinal stromal tumor presenting as peritoneal dissemination].
  • Gastrointestinal stromal tumor (GIST) is the most common mesenchymal tumor of the gastrointestinal tract, but also occurs at a lower frequency in extra-gastrointestinal regions such as omentum, mesentery, retroperitoneum and undefined abdominal sites.
  • This tumor is called extragastrointestinal stromal tumor (EGIST).
  • EGIST is mostly diagnosed as a cystic mass, but rarely occurs as a disseminated abdominal tumor.
  • Abdominal CT showed diffuse peritoneal thickening with a large amount of ascites, but no definite mass lesion.
  • Laparoscopic biopsy was performed and histologic findings showed tumor composed of epithelioid cells.
  • In the results of immunohistochemical stains, the tumor showed positive reactivity with CD117 (c-kit), CD34, vimentin and actin, but negative reactivity with desmin and S-100 protein.
  • [MeSH-major] Gastrointestinal Stromal Tumors / diagnosis. Peritoneal Neoplasms / diagnosis

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  • (PMID = 21099240.001).
  • [ISSN] 1598-9992
  • [Journal-full-title] The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi
  • [ISO-abbreviation] Korean J Gastroenterol
  • [Language] kor
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Korea (South)
  • [Chemical-registry-number] 0 / Actins; 0 / Antigens, CD34; 0 / Vimentin; EC 2.7.10.1 / Proto-Oncogene Proteins c-kit
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49. May M, Gunia S, Helke C, Braun KP, Hoschke B, Gastinger I, Marusch F: [A benign abdominal schwannoma presenting as postrenal failure--a case report]. Klin Padiatr; 2007 Jan-Feb;219(1):30-1
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  • [Title] [A benign abdominal schwannoma presenting as postrenal failure--a case report].
  • [Transliterated title] Ein benignes Schwannom des Abdomens als Ursache des postrenalen Nierenversagens--Ein Fallbericht.
  • BACKGROUND: Benign schwannomas are uncommon soft-tissue tumors in childhood.
  • The occurrence of an abdominal schwannoma effecting an acute postrenal failure has not been reported thus far.
  • Further diagnostic investigations demonstrated a 24x20x15 cm abdominal tumor, which lead to an acute postrenal failure.
  • The resection of the intraperitoneal tumor was performed completely, the histopathological examination revealed a benign schwannoma.
  • Subsequently, the renal function had rapidly to normalised and ten years after the operation he has had no tumor recurrence.
  • The clinical presentation, differential diagnosis and operative strategy for benign and malignant abdominal schwannomas are discussed.
  • [MeSH-major] Abdominal Neoplasms / complications. Hydronephrosis / etiology. Neurilemmoma / complications. Renal Insufficiency / etiology. Ureteral Obstruction / etiology

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  • (PMID = 16832781.001).
  • [ISSN] 0300-8630
  • [Journal-full-title] Klinische Pädiatrie
  • [ISO-abbreviation] Klin Padiatr
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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50. Wyler S, Huang DJ, Singer G, Schötzau A, Holzgreve W, Güth U: Metastatic involvement of the urinary tract in patients with advanced ovarian carcinoma: lessons from the autopsy for an interdisciplinary treatment approach. Eur J Gynaecol Oncol; 2009;30(2):174-7
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  • The distribution of abdominal metastatic sites with particular attention to the involvement of the urologic organs, and hydronephrosis was analyzed.
  • CONCLUSION: Hydronephrosis in late stages of ovarian carcinoma, usually attributed to extrinsic compression of the ureter by an abdominal tumor, may also be explained by ureteral metastases.
  • [MeSH-major] Carcinoma / secondary. Ovarian Neoplasms / pathology. Urologic Neoplasms / secondary
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Female. Humans. Kidney Neoplasms / secondary. Middle Aged. Ureteral Neoplasms / secondary. Urinary Bladder Neoplasms / secondary

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  • (PMID = 19480248.001).
  • [ISSN] 0392-2936
  • [Journal-full-title] European journal of gynaecological oncology
  • [ISO-abbreviation] Eur. J. Gynaecol. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Italy
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51. Mizutani S, Nakamura Y, Ogata M, Watanabe M, Tokunaga A, Tajiri T: A case of giant mucinous cystic neoplasm of the pancreas resected with laparoscopic surgery. J Nippon Med Sch; 2009 Aug;76(4):212-6
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  • [Title] A case of giant mucinous cystic neoplasm of the pancreas resected with laparoscopic surgery.
  • We report a case of giant mucinous cystic neoplasm (MCN) of the pancreas that was successfully treated with laparoscopic surgery.
  • A 29-year-old woman was admitted to our hospital for evaluation of an abdominal tumor that had been detected during a routine medical examination.
  • The tumor was diagnosed as an MCN of the pancreas.
  • [MeSH-major] Cystadenoma, Mucinous / surgery. Laparoscopy. Pancreatectomy / methods. Pancreatic Neoplasms / surgery. Splenectomy / methods

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  • (PMID = 19755797.001).
  • [ISSN] 1345-4676
  • [Journal-full-title] Journal of Nippon Medical School = Nippon Ika Daigaku zasshi
  • [ISO-abbreviation] J Nippon Med Sch
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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52. Beltran Gárate B, Morales Luna D, Quiñones Avila P, Hurtado de Mendoza F, Riva Gonzales L, Yabar A, Portugal Meza K: [Primary colorectal lymphoma of diffuse large B-cells: an experience at a general hospital]. Rev Gastroenterol Peru; 2008 Jul-Sep;28(3):235-8
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  • [Transliterated title] Linfoma de células grandes B difuso primario colorectal: experiencia en un hospital general.
  • Primary colorectal lymphoma is a very rare disease.
  • The most frequent signs and symptoms were abdominal pain (78%), diarrhea (49%) and abdominal tumor (35%).
  • [MeSH-major] Colorectal Neoplasms. Lymphoma, Large B-Cell, Diffuse
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Cecum / pathology. Colon / pathology. Cyclophosphamide / therapeutic use. Doxorubicin / therapeutic use. Female. Humans. Male. Middle Aged. Neoplasm Staging. Prednisone / therapeutic use. Rectum / pathology. Retrospective Studies. Time Factors. Vincristine / therapeutic use

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  • (PMID = 18958138.001).
  • [ISSN] 1022-5129
  • [Journal-full-title] Revista de gastroenterología del Perú : órgano oficial de la Sociedad de Gastroenterología del Perú
  • [ISO-abbreviation] Rev Gastroenterol Peru
  • [Language] spa
  • [Publication-type] Comparative Study; English Abstract; Journal Article
  • [Publication-country] Peru
  • [Chemical-registry-number] 5J49Q6B70F / Vincristine; 80168379AG / Doxorubicin; 8N3DW7272P / Cyclophosphamide; VB0R961HZT / Prednisone; CHOP protocol
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53. Dickson PV, Sims TL, Streck CJ, McCarville MB, Santana VM, McGregor LM, Furman WL, Davidoff AM: Avoiding misdiagnosing neuroblastoma as Wilms tumor. J Pediatr Surg; 2008 Jun;43(6):1159-63
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  • [Title] Avoiding misdiagnosing neuroblastoma as Wilms tumor.
  • PURPOSE: Although occasionally difficult, distinguishing abdominal neuroblastoma (NBL) from Wilms tumor (WT) at presentation is important, as surgical management differs significantly.
  • In addition, laboratory evaluation, including urinary catecholamines, should be completed before surgery when the etiology of an abdominal tumor is uncertain.

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  • (PMID = 18558200.001).
  • [ISSN] 1531-5037
  • [Journal-full-title] Journal of pediatric surgery
  • [ISO-abbreviation] J. Pediatr. Surg.
  • [Language] ENG
  • [Grant] United States / PHS HHS / / 21766; United States / NCI NIH HHS / CA / P30 CA021765-33S2; United States / NCI NIH HHS / CA / P01 CA023099; United States / NCI NIH HHS / CA / P30 CA021765; United States / NCI NIH HHS / CA / CA 23099
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Other-IDs] NLM/ NIHMS57686; NLM/ PMC3214966
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54. Nakaoka T, Uemura S, Nakagawa Y, Yano T, Oda M: Retroperitoneal ganglioneuroblastoma resected 8 years after mass screening: a case report. J Pediatr Surg; 2007 Nov;42(11):E29-32
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  • An 8-year-old girl presented with abdominal tumor that was discovered incidentally.
  • At surgery, the tumor originated from the retroperitoneal sympathetic trunk; and the histologic diagnosis was ganglioneuroblastoma, nodular (GNBn), unfavorable histology on Shimada's classification, International Neuroblastoma Staging System (INSS) stage 1.
  • There was no tumor detected, and tumor markers decreased to normal range by 18 months of age.
  • We examined her previous computed tomographic films retrospectively and noticed a mass in the same region indicating that the tumor had been there for 8 years without treatment.
  • [MeSH-major] Biomarkers, Tumor / blood. Ganglioneuroblastoma / diagnosis. Retroperitoneal Neoplasms / diagnosis

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  • (PMID = 18022424.001).
  • [ISSN] 1531-5037
  • [Journal-full-title] Journal of pediatric surgery
  • [ISO-abbreviation] J. Pediatr. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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55. Yamanaka H, Mizushima T, Mikata S, Ito T, Nonaka K, Ide H, Michiura T, Kainuma S, Iwase K: [Peritoneal dissemination from gastrointestinal stromal tumor of small intestine responding completely to imatinib mesylate (STI 571)]. Gan To Kagaku Ryoho; 2005 Dec;32(13):2125-8
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  • [Title] [Peritoneal dissemination from gastrointestinal stromal tumor of small intestine responding completely to imatinib mesylate (STI 571)].
  • The prognosis of metastatic or recurrent GISTs is poor, because these tumors resist chemotherapy and radiotherapy.
  • A 64-year-old man presented with large intra-abdominal mass.
  • The abdominal mass was phi3 x 3.5 cm in size with ascites at Douglas, as determined by computed tomography, and was diagnosed as a peritoneal relapse of GIST.
  • After 1 month of treatment with imatinib, reduction of the abdominal tumor began to be recognized on palpation.
  • Computed tomographic scanning at 11 months revealed that the tumor had completely disappeared.
  • [MeSH-major] Antineoplastic Agents / therapeutic use. Gastrointestinal Stromal Tumors / drug therapy. Jejunal Neoplasms / drug therapy. Peritoneal Neoplasms / drug therapy. Piperazines / therapeutic use. Pyrimidines / therapeutic use

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  • (PMID = 16352942.001).
  • [ISSN] 0385-0684
  • [Journal-full-title] Gan to kagaku ryoho. Cancer & chemotherapy
  • [ISO-abbreviation] Gan To Kagaku Ryoho
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Benzamides; 0 / Piperazines; 0 / Pyrimidines; 8A1O1M485B / Imatinib Mesylate
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56. Iwamoto I, Yanazume S, Fujino T, Yoshioka T, Douchi T: Leydig cell tumor in an elderly patient with complete androgen insensitivity syndrome. Gynecol Oncol; 2005 Mar;96(3):870-2
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  • [Title] Leydig cell tumor in an elderly patient with complete androgen insensitivity syndrome.
  • Testicular tumors often develop in patients with AIS, Sertoli cell tumor and seminoma being the most common types.
  • Leydig cell tumor in AIS is extremely rare.
  • CASE: A large abdominal tumor developed in a 73-year-old female patient.
  • The patient underwent the extirpation of bilateral gonads including the tumor, pelvic lymph nodes, omentum and appendix vermiformis.
  • The pathological diagnosis was malignant Leydig cell tumor of the left testis.
  • The patient showed no evidence of disease at the post-operative 1 month checkup.
  • CONCLUSION: We reported an extremely rare case of malignant Leydig cell tumor developing in an elderly AIS patient.
  • [MeSH-major] Androgen-Insensitivity Syndrome / complications. Leydig Cell Tumor / complications. Ovarian Neoplasms / complications


57. Higa F, Uchihara T, Haranaga S, Yara S, Tateyama M, Oshiro Y, Shiraishi M, Kumasaka T, Seyama K, Fujita J: Malignant epithelioid angiomyolipoma in the kidney and liver of a patient with pulmonary lymphangioleiomyomatosis: lack of response to sirolimus. Intern Med; 2009;48(20):1821-5
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  • A 26-year-old woman with lymphangioleiomyomatosis (LAM) was hospitalized for the surgical excision of a giant abdominal tumor of right kidney origin.
  • The pathological diagnosis of the tumor was conventional angiomyolipoma (AML).
  • After 8 months, 2 liver tumors appeared and grew rapidly.
  • The tumors were resected, and the pathological finding of these tumors was epithelioid AML.
  • Thereafter, metastatic multiple lung tumors appeared, and there was local recurrence of the liver tumors.
  • However, the drug did not inhibit the rapid growth of the tumor at all.
  • This finding suggests that sirolimus might not be effective against epithelioid AML, and in such cases, complete surgical resection should be the treatment of choice.
  • [MeSH-major] Angiomyolipoma / diagnosis. Kidney Neoplasms / diagnosis. Liver Neoplasms / diagnosis. Lung Neoplasms / diagnosis. Lymphangioleiomyomatosis / diagnosis. Sirolimus / therapeutic use
  • [MeSH-minor] Adult. Fatal Outcome. Female. Humans. Neoplasm Recurrence, Local / complications. Neoplasm Recurrence, Local / diagnosis. Neoplasm Recurrence, Local / drug therapy


58. Chang SC, Liao JW: Mesojejunoileac liposarcoma with intrahepatic metastasis in a dog. J Vet Med Sci; 2008 Jun;70(6):637-40
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  • The patient was an 8-year-old, male Dachshund, and was referred to our hospital owing to the significant distention of the left abdomen.
  • Neither radiography nor ultrasonography detected the actual association of the tumor with the abdominal viscera before surgery.
  • A large-sized tumor mass that adhered to the mesojejunoileum was explored by laparatomy.

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  • (PMID = 18628610.001).
  • [ISSN] 0916-7250
  • [Journal-full-title] The Journal of veterinary medical science
  • [ISO-abbreviation] J. Vet. Med. Sci.
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0W860991D6 / Deoxycytidine; 6804DJ8Z9U / Capecitabine; 80168379AG / Doxorubicin; U3P01618RT / Fluorouracil
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59. Giunti L, Bernini G, Forni M, Tucci F, Wheeler E, Sardi I: Clonality analysis of pediatric multiple tumors: two case reports and laboratory investigation. J Pediatr Hematol Oncol; 2006 Apr;28(4):241-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Clonality analysis of pediatric multiple tumors: two case reports and laboratory investigation.
  • We examined the possibility of using microsatellite and mitochondrial DNA polymorphisms as markers to detect the clonal origin of tumor cells found in the same patient.
  • We considered two children with complex tumor diseases: one with supratentorial primitive neuroectodermal tumors (PNET) and a hepatic rhabdoid tumor and another with brain and abdominal rhabdoid tumors.
  • In the first patient we found an mtDNA cytosine insertion both in the normal tissue and in the primary tumor, whereas in the hepatic tumor we detected an insertion of 2 cytosine.
  • In the second child, who had a constitutional mutation of hSNF5/INI-1, we identified the same mtDNA pattern both in normal tissue and in the abdominal tumor but not in the brain tumor, which presented three different mtDNA polymorphisms.
  • Thus, we demonstrated the same clonal origin for tumors in the first patient and different clonal origins of the tumors in the second patient.
  • Molecular examination of clonality is a useful tool to obtain information about the origin of synchronous and/or metachronous tumors found in the same patient.
  • [MeSH-major] Neoplasms / genetics

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  • (PMID = 16679923.001).
  • [ISSN] 1077-4114
  • [Journal-full-title] Journal of pediatric hematology/oncology
  • [ISO-abbreviation] J. Pediatr. Hematol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / DNA Primers; 0 / DNA, Mitochondrial
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60. Takano M, Yoshikawa T, Kato M, Aida S, Goto T, Furuya K, Kikuchi Y: Primary clear cell carcinoma of the peritoneum: report of two cases and a review of the literature. Eur J Gynaecol Oncol; 2009;30(5):575-8
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  • The most common neoplasms of the peritoneum are malignant mesothelioma and serous papillary adenocarcinoma.
  • Case 1, a 53-year-old woman, presented with upper abdominal and pelvic tumors.
  • Case 2, a 66-year-old woman, presented with massive ascites and abdominal tumor.
  • The ovaries and uterine endometrium of these cases were not affected, and the tumors were diagnosed as Stage IIIc CCC of the peritoneum origin.
  • The cases and a review of the literature suggested that residual tumor volume size determines the survival of these patients, and that the tumors show resistance to conventional platinum-based chemotherapy.
  • [MeSH-major] Adenocarcinoma, Clear Cell / pathology. Antineoplastic Combined Chemotherapy Protocols. Peritoneal Neoplasms / pathology

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  • [ErratumIn] Eur J Gynaecol Oncol. 2010;31(1):4. Yoshokawa, T [corrected to Yoshikawa, T]
  • (PMID = 19899421.001).
  • [ISSN] 0392-2936
  • [Journal-full-title] European journal of gynaecological oncology
  • [ISO-abbreviation] Eur. J. Gynaecol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Italy
  • [Chemical-registry-number] 7673326042 / irinotecan; Q20Q21Q62J / Cisplatin; XT3Z54Z28A / Camptothecin
  • [Number-of-references] 15
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61. Flores-Alvarez E, Tello-Brand SE, López-López F, Rivera-Barragán V: Peritoneal tuberculosis. Report of seven cases. Cir Cir; 2010 Jan-Feb;78(1):67-71
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  • The most frequent clinical data were abdominal pain (six patients), ascites (four patients), and abdominal tumor (three patients).
  • Abdominopelvic CT examinations revealed unilateral ovarian tumor in four patients, bilateral ovarian tumor in two patients, ascites in four patients, and retroperitoneal adenopathy in one patient.
  • All patients had a preoperative diagnosis of malignant tumor.
  • Diagnoses should be considered in all patients with ascites, adnexal tumors and elevated serum CA-125 levels.
  • [MeSH-minor] Abdominal Pain / etiology. Adult. Antitubercular Agents / therapeutic use. Ascites / etiology. Biomarkers. CA-125 Antigen / blood. Combined Modality Therapy. Elective Surgical Procedures. Female. Humans. Immunocompromised Host. Laparotomy. Lymphoma / diagnosis. Male. Mexico / epidemiology. Middle Aged. Ovarian Neoplasms / diagnosis. Ovariectomy. Peritoneal Neoplasms / diagnosis. Peritoneal Neoplasms / secondary. Young Adult

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  • (PMID = 20226130.001).
  • [ISSN] 0009-7411
  • [Journal-full-title] Cirugía y cirujanos
  • [ISO-abbreviation] Cir Cir
  • [Language] eng; spa
  • [Publication-type] Journal Article; Multicenter Study
  • [Publication-country] Mexico
  • [Chemical-registry-number] 0 / Antitubercular Agents; 0 / Biomarkers; 0 / CA-125 Antigen
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62. Madani A, Benhmiddoune L, Zafad S, Harif M, Quessar A, Benchekroun S: [Treatment of childhood Burkitt lymphoma according to LMB89 protocol in Casablanca]. Bull Cancer; 2005 Feb;92(2):193-8
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  • [Transliterated title] Traitement du lymphome de Burkitt de l'enfant par le protocole LMB89 à Casablanca.
  • Seventy three percent of patients had abdominal tumor and 10% had maxillary tumor.

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  • (PMID = 15749649.001).
  • [ISSN] 1769-6917
  • [Journal-full-title] Bulletin du cancer
  • [ISO-abbreviation] Bull Cancer
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 04079A1RDZ / Cytarabine; 5J49Q6B70F / Vincristine; 6PLQ3CP4P3 / Etoposide; 80168379AG / Doxorubicin; 8N3DW7272P / Cyclophosphamide; Q573I9DVLP / Leucovorin; VB0R961HZT / Prednisone; WI4X0X7BPJ / Hydrocortisone; YL5FZ2Y5U1 / Methotrexate; LMB89 protocol
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63. Kanno A, Hatori M, Hosaka M, Kishimoto KN, Watanuki M, Watanabe M, Itoi E: Multiple bone metastasis of sclerosing epithelioid fibrosarcoma 12 years after initial surgery-increasing ki-67 labeling index. Sarcoma; 2009;2009:953750

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  • At 18, a tumor in the abdominal wall was excised.
  • At 23, the tumor recurred which was removed again.
  • Histological examination of the chest wall tumor showed epithelioid cells arranged like alveolar pattern with dense collagen stroma.
  • Abdominal and the rib tumors showed the same immunohistochemistrical expression.
  • It is noteworthy that the tumor cells of the rib lesion showed increased cellularity, and its Ki-67 activity was higher as compared with the abdominal tumor, suggestive of progression of malignancy of SEF.

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  • [Cites] Histopathology. 1998 Oct;33(4):354-60 [9822926.001]
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  • (PMID = 19343182.001).
  • [ISSN] 1357-714X
  • [Journal-full-title] Sarcoma
  • [ISO-abbreviation] Sarcoma
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Egypt
  • [Other-IDs] NLM/ PMC2662323
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64. Kitagawa H, Okabayashi T, Nishimori I, Kobayashi M, Sugimoto T, Akimori T, Kohsaki T, Miyaji E, Onishi S, Araki K: Rapid growth of mucinous cystic adenoma of the pancreas following pregnancy. Int J Gastrointest Cancer; 2006;37(1):45-8
MedlinePlus Health Information. consumer health - Tumors and Pregnancy.

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  • At 8 mo postpartum, she became aware of an upper abdominal tumor.
  • Abdominal computed tomography and upper abdominal ultrasonography revealed a large cystic mass in the body of the pancreas.
  • The patient underwent tumor resection at 11 mo postpartum.
  • Pathological examination of the tumor revealed mucin-producing columnar epithelial cells lining the cystic wall with ovarian-type stromal tissue and no findings indicative of malignancy, giving a diagnosis of mucinous cystic adenoma of the pancreas.
  • Postpartum rapid growth of a benign mucinous cystic neoplasm might be linked to the production of female sex hormones during lactation.
  • [MeSH-major] Adenoma / pathology. Cystadenocarcinoma, Mucinous / pathology. Pancreatic Neoplasms / pathology. Pregnancy Complications, Neoplastic / pathology

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  • (PMID = 17290080.001).
  • [ISSN] 1537-3649
  • [Journal-full-title] International journal of gastrointestinal cancer
  • [ISO-abbreviation] Int J Gastrointest Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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65. de León DC, Pérez-Montiel D, Chanona-Vilchis J, Dueñas-González A, Villavicencio-Valencia V, Zavala-Casas G: Primary retroperitoneal mucinous cystadenocarcinoma: report of two cases. World J Surg Oncol; 2007;5:5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • RESULTS: One case presented as pelvic tumor, was treated with surgical resection of the disease, but manifested with recurrent disease a few months later despite use of chemotherapy.
  • The second case involved a patient with diagnosis of abdominal tumor; during laparotomy, a retroperitoneal tumor was found and was totally removed.
  • At follow-up, the patient is disease-free with no other treatment.
  • [MeSH-major] Cystadenocarcinoma, Mucinous / pathology. Retroperitoneal Neoplasms / pathology

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  • (PMID = 17224073.001).
  • [ISSN] 1477-7819
  • [Journal-full-title] World journal of surgical oncology
  • [ISO-abbreviation] World J Surg Oncol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC1783654
  • [General-notes] NLM/ Original DateCompleted: 20070723
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66. Miyake M, Tateishi U, Maeda T, Arai Y, Seki K, Hasegawa T, Sugimura K: A case of ganglioneuroma presenting abnormal FDG uptake. Ann Nucl Med; 2006 Jun;20(5):357-60
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  • A 26-year-old woman presented to the hospital with a slowly growing abdominal tumor without symptoms.
  • Computed tomography (CT) revealed huge retroperitoneal tumors and fused 18F-fluorodeoxyglucose positron emission tomography (FDG-PET)/CT image showed abnormal accumulation of FDG in tumors with maximal standardized uptake value of 2.02.
  • However, a second primary malignant tumor, such as malignant peripheral nerve sheath tumor arising in ganglioneuroma, could not be ruled out.
  • Pathological investigation may be needed to differentiate ganglioneuroma from other malignant tumors and, therefore, FDG-PET/CT findings can be helpful for biopsy planning.
  • [MeSH-major] Abdominal Neoplasms / radionuclide imaging. Fluorodeoxyglucose F18. Neuroma / radionuclide imaging

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  • (PMID = 16878708.001).
  • [ISSN] 0914-7187
  • [Journal-full-title] Annals of nuclear medicine
  • [ISO-abbreviation] Ann Nucl Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Radiopharmaceuticals; 0Z5B2CJX4D / Fluorodeoxyglucose F18
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67. Shinohara H, Ishii H, Kakuyama M, Fukuda K: [Morbidly obese patient with a huge ovarian tumor who was intubated while awake using airway scope in lateral decubitus position]. Masui; 2010 May;59(5):625-8
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  • [Title] [Morbidly obese patient with a huge ovarian tumor who was intubated while awake using airway scope in lateral decubitus position].
  • A morbidly obese woman with a huge ovarian tumor was scheduled to undergo tumor resection under general anesthesia.
  • To avoid circulatory collapse and reexpansion pulmonary edema, the content of the huge ovarian tumor was aspirated through a small drainage tube to reduce volume and weight of the tumor.
  • Then resection of the ovarian tumor and abdominal wall tissue was performed in supine position.
  • [MeSH-major] Anesthesia, General. Intubation, Intratracheal / instrumentation. Intubation, Intratracheal / methods. Laryngoscopes. Obesity, Morbid / complications. Ovarian Neoplasms / complications. Ovarian Neoplasms / surgery. Supine Position. Wakefulness

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  • (PMID = 20486577.001).
  • [ISSN] 0021-4892
  • [Journal-full-title] Masui. The Japanese journal of anesthesiology
  • [ISO-abbreviation] Masui
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Methyl Ethers; 38LVP0K73A / sevoflurane
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68. Iwama T, Kuwabara K, Ushiama M, Yoshida T, Sugano K, Ishida H: Identification of somatic APC mutations in recurrent desmoid tumors in a patient with familial adenomatous polyposis to determine actual recurrence of the original tumor or de novo occurrence. Fam Cancer; 2009;8(1):51-4
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  • [Title] Identification of somatic APC mutations in recurrent desmoid tumors in a patient with familial adenomatous polyposis to determine actual recurrence of the original tumor or de novo occurrence.
  • A 25-year-old female with familial adenomatous polyposis (FAP) presented with an abdominal tumor just below the scar due to a colectomy performed 15 months previously.
  • This tumor (tumor A) measured 7 cm in diameter, was diagnosed as a desmoid tumor of the abdominal wall, and was excised.
  • Despite the subsequent administration of sulindac (300 mg daily for 1 year), a desmoid tumor recurred at the same site.
  • Excision was performed again when the tumor was 8 cm in diameter, and examination revealed it to consist of a large tumor (B) and a small tumor (C) that bulged out from tumor B.
  • Two somatic mutations were observed in tumor A: a TCAA deletion at codon 1068 and a deletion of a codon at bp 1192-2097.
  • In tumor B, a somatic mutation was found at codon 1041 changing CAA to TAA.
  • We could not detect any somatic mutations in tumor C.
  • We conclude that somatic mutation analysis of the APC gene can be used to identify whether a recurrent desmoid tumor in a patient with FAP is a new primary tumor or a recurrence from microscopic remnants of the original tumor.
  • [MeSH-major] Adenomatous Polyposis Coli / genetics. Fibromatosis, Aggressive / genetics. Genes, APC. Neoplasm Recurrence, Local / genetics. Neoplasms, Multiple Primary / genetics

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  • (PMID = 18704758.001).
  • [ISSN] 1573-7292
  • [Journal-full-title] Familial cancer
  • [ISO-abbreviation] Fam. Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
  • [Chemical-registry-number] 0 / Antineoplastic Agents
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69. Fujishima N, Fujishima M, Inomata M, Yamanaka Y, Saitoh K, Kameoka Y, Yoshioka T, Saitoh H, Takahashi N, Hirokawa M, Sawada K: [Early relapse of Burkitt's lymphoma with t(8;14) and t(14;18) after rituximab-combined CODOX-M and IVAC therapy]. Rinsho Ketsueki; 2007 Apr;48(4):326-31
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  • A 43-year-old female was admitted with therapy-resistant pancreatitis and an abdominal tumor around the pancreatic head.
  • Although CODOX-M and IVAC therapy combined with rituximab achieved complete remission, she died of rapid progressive disease during whole brain irradiation before autologous peripheral blood stem cell transplantation.
  • A more effective therapy remains to be established for the treatment of this disease.
  • [MeSH-minor] Adult. Antibodies, Monoclonal / administration & dosage. Antibodies, Monoclonal, Murine-Derived. Cyclophosphamide / administration & dosage. Cytarabine / administration & dosage. Disease Progression. Doxorubicin / administration & dosage. Etoposide / administration & dosage. Fatal Outcome. Female. Humans. Ifosfamide / administration & dosage. Methotrexate / administration & dosage. Recurrence. Remission Induction. Rituximab. Vincristine / administration & dosage

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  • (PMID = 17515125.001).
  • [ISSN] 0485-1439
  • [Journal-full-title] [Rinshō ketsueki] The Japanese journal of clinical hematology
  • [ISO-abbreviation] Rinsho Ketsueki
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Antibodies, Monoclonal; 0 / Antibodies, Monoclonal, Murine-Derived; 04079A1RDZ / Cytarabine; 4F4X42SYQ6 / Rituximab; 5J49Q6B70F / Vincristine; 6PLQ3CP4P3 / Etoposide; 80168379AG / Doxorubicin; 8N3DW7272P / Cyclophosphamide; UM20QQM95Y / Ifosfamide; YL5FZ2Y5U1 / Methotrexate; ANAVACYM protocol; IVAC protocol
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70. Elharroudi T, Ismaili N, Errihani H, Jalil A: Primary lymphoma of the ovary. J Cancer Res Ther; 2008 Oct-Dec;4(4):195-6
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  • Involvement of the ovary by malignant lymphoma is a well-known late manifestation of disseminated nodal disease.
  • Computed tomography revealed an abdominal tumor measuring 20 cm in diameter, without enlarged lymph nodes.
  • The tumor was classified as a diffuse large B-cell lymphoma.
  • She has now been without disease for 7 months after the surgery.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Lymphoma, Non-Hodgkin / diagnosis. Lymphoma, Non-Hodgkin / drug therapy. Ovarian Neoplasms / diagnosis. Ovarian Neoplasms / drug therapy
  • [MeSH-minor] Adult. Antigens, Neoplasm / chemistry. Cyclophosphamide / therapeutic use. Doxorubicin / therapeutic use. Female. Humans. Positron-Emission Tomography / methods. Prednisolone / therapeutic use. Prognosis. Tomography, X-Ray Computed / methods. Treatment Outcome. Vincristine / therapeutic use

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  • (PMID = 19052394.001).
  • [ISSN] 1998-4138
  • [Journal-full-title] Journal of cancer research and therapeutics
  • [ISO-abbreviation] J Cancer Res Ther
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
  • [Chemical-registry-number] 0 / Antigens, Neoplasm; 5J49Q6B70F / Vincristine; 80168379AG / Doxorubicin; 8N3DW7272P / Cyclophosphamide; 9PHQ9Y1OLM / Prednisolone; VAP-cyclo protocol
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71. Yearley JH, King N, Liu X, Curran EH, O'Neil SP: Biphasic malignant testicular sex cord-stromal tumor in a cotton-top tamarin (Saguinus oedipus) with review of the literature. Vet Pathol; 2008 Nov;45(6):922-7
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  • [Title] Biphasic malignant testicular sex cord-stromal tumor in a cotton-top tamarin (Saguinus oedipus) with review of the literature.
  • The animal was castrated, and histologic examination revealed a biphasic sex cord-stromal tumor, with one region resembling Sertoli-cell tumor and one region resembling granulosa-cell tumor, with extensive microfollicular pattern and many Call-Exner bodies.
  • Eight months after castration, the animal was euthanized on discovery of a caudal abdominal mass that displaced organs, was highly infiltrative, and extended into the paravertebral musculature with lysis of vertebral bone.
  • Histologic examination of the abdominal tumor showed multifocal formation of Call-Exner bodies in an otherwise highly dedifferentiated population.
  • Positive immunolabeling for alpha inhibin confirmed the sex cord-stromal origin of the abdominal and paravertebral tumor masses.
  • This case has similarities to malignant testicular granulosa-cell tumor of humans.

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  • (PMID = 18984797.001).
  • [ISSN] 0300-9858
  • [Journal-full-title] Veterinary pathology
  • [ISO-abbreviation] Vet. Pathol.
  • [Language] ENG
  • [Grant] United States / NCRR NIH HHS / RR / K01RR24120; United States / NCRR NIH HHS / RR / T32 RR007000; United States / NCRR NIH HHS / RR / RR00168; United States / NCRR NIH HHS / RR / P51 RR000168; United States / NCRR NIH HHS / RR / K26 RR000168; United States / NCRR NIH HHS / RR / T32 RR007000-32; United States / NCRR NIH HHS / RR / RR007000-32; United States / NCRR NIH HHS / RR / K01 RR024120
  • [Publication-type] Case Reports; Journal Article; Research Support, N.I.H., Extramural; Review
  • [Publication-country] United States
  • [Number-of-references] 37
  • [Other-IDs] NLM/ NIHMS93232; NLM/ PMC2660595
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72. Matsuda A, Sasajima K, Matsutani T, Maruyama H, Miyamoto M, Yokoyama T, Suzuki S, Suzuki H, Tajiri T: Aggressive undifferentiated colon carcinoma producing granulocyte-colony stimulating factor: report of a case. Surg Today; 2009;39(11):990-3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • A 52-year-old Japanese man presented with a rapidly growing, aggressive abdominal tumor, and severe leukocytosis (63 000/mm(3)).
  • The tumor cells were positive for G-CSF on immunohistochemical staining.
  • His general condition deteriorated rapidly and he died of residual tumor growth on postoperative day 24.
  • [MeSH-major] Carcinoma / secretion. Colonic Neoplasms / secretion. Granulocyte Colony-Stimulating Factor / secretion
  • [MeSH-minor] Biomarkers, Tumor / secretion. Colectomy / methods. Colonoscopy. Diagnosis, Differential. Fatal Outcome. Follow-Up Studies. Humans. Immunohistochemistry. Male. Middle Aged

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  • (PMID = 19882323.001).
  • [ISSN] 1436-2813
  • [Journal-full-title] Surgery today
  • [ISO-abbreviation] Surg. Today
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 143011-72-7 / Granulocyte Colony-Stimulating Factor
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73. Mitsuhashi A, Nagai Y, Suzuka K, Yamazawa K, Nojima T, Nikaido T, Ishikura H, Matsui H, Shozu M: Primary synovial sarcoma in fallopian tube: case report and literature review. Int J Gynecol Pathol; 2007 Jan;26(1):34-7
Genetic Alliance. consumer health - Synovial sarcoma.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Synovial sarcoma, a malignant mesenchymal neoplasm, occurs mostly near the joints of the extremities and occasionally outside the joint such as lung.
  • Recurrent abdominal tumor, observed at 12 month after the initial surgery and following chemotherapy using doxorubicin, cisplatin and ifosfamide, partially responded to chemotherapy using paclitaxel and carboplatin and, then, optimal surgery was performed.
  • [MeSH-major] Fallopian Tube Neoplasms / pathology. Sarcoma, Synovial / pathology

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  • (PMID = 17197895.001).
  • [ISSN] 0277-1691
  • [Journal-full-title] International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists
  • [ISO-abbreviation] Int. J. Gynecol. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Oncogene Proteins, Fusion; 0 / SYT-SSX fusion protein
  • [Number-of-references] 12
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74. Castillo O, Frisancho O, Contardo C, Morales D, Garatea R: [Gastrointestinal stromal tumor (GIST) of Duodenum: Case report]. Rev Gastroenterol Peru; 2010 Jul-Sep;30(3):241-6
MedlinePlus Health Information. consumer health - Intestinal Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Gastrointestinal stromal tumor (GIST) of Duodenum: Case report].
  • [Transliterated title] Tumor estromal gastrointestinal en duodeno.
  • During that hospitalization, it was found a duodenal tumor by tomography; however, no further studies or follow up on this finding was done.
  • She presented with fever, abdominal pain and a palpable abdominal tumor in the right upper quadrant for a month.
  • We realized a three-phase multislice spiral tomography with pancreatic curved reconstruction, which allowed to identified an ovoid tumor of 80 x 60 mm, with an area of central necrosis and intense contrast enhancement (arterial phase), located between the second and third duodenal portion, near the head of the pancreas.
  • The patient underwent tumor resection without complication and the histologic diagnosis of the surgical specimen revealed a duodenal stromal tumor (GIST) with extraluminal transmural growth.
  • We presented this case because of its unusual presentation of this tumor.
  • [MeSH-major] Duodenal Neoplasms. Gastrointestinal Stromal Tumors

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  • [ErratumIn] Rev Gastroenterol Peru. 2010 Oct-Dec;30(4):373
  • (PMID = 20924435.001).
  • [ISSN] 1022-5129
  • [Journal-full-title] Revista de gastroenterología del Perú : órgano oficial de la Sociedad de Gastroenterología del Perú
  • [ISO-abbreviation] Rev Gastroenterol Peru
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Peru
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75. Muraoka I, Ohno Y, Kamitamari A, Okada M, Moriuchi H, Kanematsu T: Congenital occurrence of solitary infantile myofibromatosis of the spleen. J Pediatr Surg; 2008 Jan;43(1):227-30
Genetic Alliance. consumer health - Infantile myofibromatosis.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Infantile myofibromatosis (IM) is a rare soft tissue tumor of infancy and childhood.
  • We report the case of a newborn girl with an abdominal tumor discovered at 32 weeks of gestation by fetal ultrasound.
  • She underwent a laparotomy for an unexplained abdominal mass 20 days after birth.
  • The tumor originated from the spleen and was removed by splenectomy.
  • Based on the histological examinations, the tumor was diagnosed as an IM.
  • Although extremely rare during the neonatal period, solitary type IM should be considered as a differential diagnosis of the splenic tumor.
  • [MeSH-major] Myofibromatosis / congenital. Myofibromatosis / surgery. Splenectomy / methods. Splenic Neoplasms / congenital. Splenic Neoplasms / surgery

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  • (PMID = 18206487.001).
  • [ISSN] 1531-5037
  • [Journal-full-title] Journal of pediatric surgery
  • [ISO-abbreviation] J. Pediatr. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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76. Hasiakos D, Papakonstantinou K, Bacanu AM, Argeitis J, Botsis D, Vitoratos N: Clinical experience of five fetal ovarian cysts: diagnosis and follow-up. Arch Gynecol Obstet; 2008 Jun;277(6):575-8
MedlinePlus Health Information. consumer health - Ovarian Cysts.

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  • BACKGROUND: Ovarian cysts are the most frequent type of abdominal tumor, in female newborns.

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  • (PMID = 18034256.001).
  • [ISSN] 0932-0067
  • [Journal-full-title] Archives of gynecology and obstetrics
  • [ISO-abbreviation] Arch. Gynecol. Obstet.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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77. Kamil S, Biswas M, Imran A, Islam R, Mukhtar A, Joshi S: Successful surgical resection of advanced gastrointestinal stromal tumor post neoadjuvent therapy. Libyan J Med; 2009 Jun 01;4(2):83-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Successful surgical resection of advanced gastrointestinal stromal tumor post neoadjuvent therapy.
  • We report a case of a 48-year-old Indian male who presented with swelling and firmness in his left upper part of the abdomen of one month duration with anorexia and weight loss.
  • Initial examination revealed an intra abdominal mass of around 16.8x11.0x24.5cm with minimal left sided pleural effusion.
  • A biopsy from the mass confirmed the diagnosis of gastrointestinal stromal tumour (GISTs) as supported by immmunohistochemistry results which showed strong positivity for c-kit while stains for smooth muscle actin, desmin, myoglobin, S100 Protein and cytokerstin remained negative.
  • The patient was not suitable for surgical intervention in view of advanced tumor, and Imatinib Mesylate 400mg daily was started with the aim of making the tumor operable.
  • It then resulted in gradual tumor regression, following which the patient underwent successful tumor resection.
  • Post surgical resection patient had no radiological evidence of intra abdominal tumor but mild left sided pleural effusion with left lower lobe atelectasis.

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  • (PMID = 21483516.001).
  • [ISSN] 1993-2820
  • [Journal-full-title] The Libyan journal of medicine
  • [ISO-abbreviation] Libyan J Med
  • [Language] ENG
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC3066724
  • [Keywords] NOTNLM ; Gastrointestinal stromal tumor / Imatinib mesylate / Immunohistochemistry / Surgery
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78. Eroles Vega G, Mecina Gutiérrez AB, Fernández García C, Mancebo Plaza AB, Riva Jiménez Ide L: [Liver abscess: retrospective review of 68 cases]. An Med Interna; 2008 Jul;25(7):335-41

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Transliterated title] Abscesos hepáticos: análisis retrospectivo de 68 casos.
  • A history of neurological disease or abdominal tumor, and multiple LA are associated with an increased complication rate.

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  • (PMID = 19295993.001).
  • [ISSN] 0212-7199
  • [Journal-full-title] Anales de medicina interna (Madrid, Spain : 1984)
  • [ISO-abbreviation] An Med Interna
  • [Language] spa
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Spain
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79. Yamaguchi T, Takahashi H, Kagawa R, Takeda R, Sakata S, Nishizaki D, Takamatsu T, Iwasa Y: Surgical resection combined with CHOP chemotherapy plus rituximab for a patient with advanced mesenteric diffuse large B cell lymphoma. Hepatogastroenterology; 2008 May-Jun;55(84):891-4
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • A 78 year old man was referred to the Rakuwakai-Otowa Hospital due to a left lower abdominal tumor.
  • Abdominal CT and MRI showed a bowel-like mass in the left lower abdominal cavity.
  • Abdominal US revealed lymph node swellings at the paraaortic region.
  • [MeSH-major] Antibodies, Monoclonal / administration & dosage. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Lymphoma, Large B-Cell, Diffuse / drug therapy. Lymphoma, Large B-Cell, Diffuse / surgery. Mesentery. Peritoneal Neoplasms / drug therapy. Peritoneal Neoplasms / surgery
  • [MeSH-minor] Aged. Antibodies, Monoclonal, Murine-Derived. Chemotherapy, Adjuvant. Colon, Sigmoid / pathology. Colon, Sigmoid / surgery. Combined Modality Therapy. Cyclophosphamide / administration & dosage. Doxorubicin / administration & dosage. Humans. Ileum / pathology. Ileum / surgery. Lymph Nodes / pathology. Magnetic Resonance Imaging. Male. Neoplasm Invasiveness. Neoplasm Staging. Prednisolone / administration & dosage. Rituximab. Tomography, X-Ray Computed. Vincristine / administration & dosage

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  • Hazardous Substances Data Bank. RITUXIMAB .
  • Hazardous Substances Data Bank. DOXORUBICIN .
  • Hazardous Substances Data Bank. CYCLOPHOSPHAMIDE .
  • Hazardous Substances Data Bank. PREDNISOLONE .
  • Hazardous Substances Data Bank. VINCRISTINE .
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  • (PMID = 18705290.001).
  • [ISSN] 0172-6390
  • [Journal-full-title] Hepato-gastroenterology
  • [ISO-abbreviation] Hepatogastroenterology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Greece
  • [Chemical-registry-number] 0 / Antibodies, Monoclonal; 0 / Antibodies, Monoclonal, Murine-Derived; 4F4X42SYQ6 / Rituximab; 5J49Q6B70F / Vincristine; 80168379AG / Doxorubicin; 8N3DW7272P / Cyclophosphamide; 9PHQ9Y1OLM / Prednisolone; VAP-cyclo protocol
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80. Csak T, Folhoffer A, Horvath A, Halász J, Diczházi C, Schaff Z, Szalay F: Holmes-Adie syndrome, autoimmune hepatitis and celiac disease: a case report. World J Gastroenterol; 2006 Mar 7;12(9):1485-7
MedlinePlus Health Information. consumer health - Celiac Disease.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Holmes-Adie syndrome, autoimmune hepatitis and celiac disease: a case report.
  • No tumor or other neurological abnormality was found.
  • Abdominal tumor was detected by ultrasound.
  • The surgically removed tumor was histologically a benign mesenteric multicystic lymphangioma.Simultaneously, celiac disease was diagnosed.Gluten-free diet resulted in a significant improvement of celiac disease,but not of autoimmune hepatitis.
  • The patient was a homozygous carrier for HLA DQ2 antigen characteristic for celiac disease and heterozygous for HLA DR3 B8 frequent in autoimmune liver diseases.
  • Our novel observation on association of Holmes-Adie syndrome with autoimmune hepatitis and celiac disease is suggestive for a common immunological background for all three entities present in a patient with mesenteric multicystic lymphangioma.
  • [MeSH-major] Adie Syndrome / complications. Celiac Disease / complications. Hepatitis, Autoimmune / complications
  • [MeSH-minor] Adult. Female. Humans. Lymphangioma, Cystic / complications. Lymphangioma, Cystic / diagnosis. Peritoneal Neoplasms / complications. Peritoneal Neoplasms / diagnosis

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  • (PMID = 16552828.001).
  • [ISSN] 1007-9327
  • [Journal-full-title] World journal of gastroenterology
  • [ISO-abbreviation] World J. Gastroenterol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] China
  • [Other-IDs] NLM/ PMC4124337
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81. Suzuki N, Yoshino S, Somura H, Ueno T, Oka M: [A case of rapid growth GIST successfully treated with resection after long-term use of imatinib]. Gan To Kagaku Ryoho; 2009 Nov;36(12):2354-6
Hazardous Substances Data Bank. IMATINIB MESYLATE .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • We report a case of rapid growth GIST successfully treated with resection, which imatinib controlled it as a stable disease for three years.
  • A 68-year-old woman underwent simple hysterectomy and bilateral oophorectomy for the pelvic tumor.
  • After diagnosed as high risk GIST, the patient was treated with imatinib at a dose of 400 mg/day, and the tumor was controlled as a stable disease for 3 years.
  • At the end of 2008, lower abdominal tumor grew rapidly and intra-abdominal hemorrhage appeared.
  • Although sunitinib was administered at a dose of 37.5 mg/day, the tumor was enlarged, and sunitinib was stopped because the patient developed grade 3 diarrhea.
  • IVR was tried to control abdominal hemorrhage, but it was unsuccessful.
  • In January 2009, the resection of main tumor was performed to control abdominal hemorrhage.
  • [MeSH-major] Abdominal Neoplasms / therapy. Antineoplastic Agents / therapeutic use. Gastrointestinal Stromal Tumors / therapy. Piperazines / therapeutic use. Pyrimidines / therapeutic use

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  • (PMID = 20037420.001).
  • [ISSN] 0385-0684
  • [Journal-full-title] Gan to kagaku ryoho. Cancer & chemotherapy
  • [ISO-abbreviation] Gan To Kagaku Ryoho
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Benzamides; 0 / Piperazines; 0 / Pyrimidines; 8A1O1M485B / Imatinib Mesylate
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82. Swenson J, Carpenter JW, Janardhan KS, Ketz-Riley C, Brinkman E: Paresis in an Asian small clawed otter (Aonyx cinereus) associated with vertebral and ischial osteolysis caused by a malignant lymphangiosarcoma. J Zoo Wildl Med; 2008 Jun;39(2):236-43

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • A 10-yr-old male intact Asian small clawed otter (Aonyx cinerus) was presumptively diagnosed by histopathology and immunohistochemistry with lymphangiosarcoma after bony destruction of the ischium and spinal column from local tumor invasion had caused progressive signs of hind limb lameness and paresis/paralysis, which led to humane euthanasia.
  • At necropsy, the primary tumor was identified as a flocculent mass present under the caudal lumbar vertebrae.
  • The tumor had metastasized to at least two different sites within the spleen.
  • The abdominal tumor was confirmed to be of endothelial origin by the use of immunohistochemical staining for factor VIII-related antigen and was confirmed as lymphatic origin versus vascular origin because of the lack of red blood cells within the vessels.
  • This is the first report of lymphangiosarcoma, an uncommon malignant neoplasm of lymphatic origin, in a mustelid and the first report of neoplastic disease in an Asian small clawed otter.
  • In addition, the presentation of hind limb paresis associated with bony lysis because of local tumor invasion has not been previously reported with lymphangiosarcoma in humans, domestic animals, or nondomestic animals.

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  • (PMID = 18634215.001).
  • [ISSN] 1042-7260
  • [Journal-full-title] Journal of zoo and wildlife medicine : official publication of the American Association of Zoo Veterinarians
  • [ISO-abbreviation] J. Zoo Wildl. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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83. Nakamura Y, Tajiri T, Uchida E, Arima Y, Aimoto T, Katsuno A, Naito Z: Changes to levels of serum neuron-specific enolase in a patient with small cell carcinoma of the pancreas. J Hepatobiliary Pancreat Surg; 2005;12(1):93-8
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Small cell carcinoma (SCC) of the pancreas is a rare disease, with an extremely poor prognosis; only 24 cases have been reported in the literature.
  • A 69-year-old woman presented with an abdominal tumor and pain.
  • Initially, the tumor disappeared completely on computed tomography (CT) scans, but she died of disease recurrence 3 months after completing the chemotherapy.
  • Changes in serum neuron-specific enolase (NSE) levels were monitored constantly during the progress of the disease.
  • NSE levels had already increased above the upper limit of normal 8 months before the patient's admission to our hospital, and levels changed concurrently not only with tumor growth but also subsequently with remission and then relapse of the disease after treatment.
  • [MeSH-major] Carcinoma, Small Cell / blood. Pancreatic Neoplasms / blood. Phosphopyruvate Hydratase / blood
  • [MeSH-minor] Aged. Biomarkers, Tumor / blood. Female. Humans

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  • (PMID = 15754108.001).
  • [ISSN] 0944-1166
  • [Journal-full-title] Journal of hepato-biliary-pancreatic surgery
  • [ISO-abbreviation] J Hepatobiliary Pancreat Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; EC 4.2.1.11 / Phosphopyruvate Hydratase
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84. Chorianopoulos D, Stratakos G: Lymphangioleiomyomatosis and tuberous sclerosis complex. Lung; 2008 Jul-Aug;186(4):197-207
MedlinePlus Health Information. consumer health - Tuberous Sclerosis.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Lymphangioleiomyomatosis (LAM) is a rare multisystemic disease of women of child-bearing age and affects mainly the lungs, promoting cystic destruction of lung parenchyma or leading to abdominal tumor formation (e.g., angiomyolipomas, lymphangioleiomyomas).
  • LAM can arise sporadically or in association with tuberous sclerosis complex (TSC), an autosomal inherited syndrome characterized by hamartoma-like tumor growth and pathologic features that are distinct from manifestations of pulmonary LAM.
  • Both of these genes are tumor suppressor genes encoding hamartin (TSC1) and tuberin (TSC2).
  • Sporadic LAM is correlated with a mutation in the TSC2 gene and tuberin appears to play a central role in the pathogenesis of the disease.
  • A TSC2 loss or mutation leads to disruption of the tuberin-hamartin heteromer and dysregulation of S6K1 activation leading to aberrant cell proliferation seen in LAM disease.
  • The extremely diverse clinical and radiologic features of the disease and the complex therapeutic approach are reviewed in detail.
  • As long as newer therapeutic agents do not change this picture, lung transplantation remains the last hope for patients with respiratory failure at the advanced stage of the disease.
  • [MeSH-minor] Disease Progression. Genetic Predisposition to Disease. Humans. Matrix Metalloproteinases / metabolism. Risk Factors. Tissue Inhibitor of Metalloproteinases / metabolism. Treatment Outcome


85. Engin G: Computed tomography enteroclysis in the diagnosis of intestinal diseases. J Comput Assist Tomogr; 2008 Jan-Feb;32(1):9-16
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  • Computed tomography enteroclysis is the examination of choice for patients with symptoms of intermittent small bowel obstruction, especially when there is a history of prior complex abdominal surgery, abdominal tumor, radiation therapy, and also in high grade obstructions with suspicion of extraintestinal internal fistula.
  • Computed tomography enteroclysis is becoming the first-line modality for the evaluation of advanced and complicated small bowel Crohn disease.
  • Computed tomography enteroclysis can also become an important complementary imaging technique to capsule endoscopy in the assessment of small bowel neoplasms and occult gastrointestinal hemorrhage.

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  • (PMID = 18303282.001).
  • [ISSN] 0363-8715
  • [Journal-full-title] Journal of computer assisted tomography
  • [ISO-abbreviation] J Comput Assist Tomogr
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Contrast Media
  • [Number-of-references] 45
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86. Poirot CJ, Martelli H, Genestie C, Golmard JL, Valteau-Couanet D, Helardot P, Pacquement H, Sauvat F, Tabone MD, Philippe-Chomette P, Esperou H, Baruchel A, Brugieres L: Feasibility of ovarian tissue cryopreservation for prepubertal females with cancer. Pediatr Blood Cancer; 2007 Jul;49(1):74-8
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  • In 16 cases, the ovary was harvested during laparotomy to resect a residual abdominal tumor.
  • None of the cases had visible ovarian tumor components.
  • [MeSH-major] Cryopreservation / methods. Neoplasms / drug therapy. Organ Preservation. Ovary. Reproductive Techniques, Assisted


87. Colovic R, Grubor N, Micev M, Radak V: Hepatocellular adenoma with malignant alteration. Hepatogastroenterology; 2007 Mar;54(74):386-8
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  • Hepatocellular adenoma is a rare benign tumor of the liver which appears almost exclusively in women taking oral contraceptives.
  • Malignant alteration of the tumor is very rare with about 12 reported cases. Case outline.
  • We present a 70-year-old woman who had not taken either oral contraceptive or other hormones ever in her life and in whom an abdominal tumor was discovered during the regular check-up for arterial hypertension.
  • During an open surgery a solitary, unilobular, spherical, well demarcated tumor on the lower surface of the segments IVb, V and VI of the liver, 115 x 100 x 90 mm in diameter was excised.
  • [MeSH-major] Adenoma, Liver Cell / pathology. Cell Transformation, Neoplastic / pathology. Liver Neoplasms / pathology

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  • (PMID = 17523280.001).
  • [ISSN] 0172-6390
  • [Journal-full-title] Hepato-gastroenterology
  • [ISO-abbreviation] Hepatogastroenterology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Greece
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88. Ochoa Urdangarain O, Hermida Pérez JA, Montes de Oca JO: [Obstructive anuria secondary to left external iliac artery aneurysm. Case report]. Arch Esp Urol; 2006 Apr;59(3):281-4

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  • [Transliterated title] Anuria obstructiva provocada por aneurisma de la arteria ilíaca externa izquierda. Presentación de un caso.
  • Hydronephrosis of the solitary left kidney due to an aneurysmatic tumor of the external iliac artery was diagnosed after performing various tests (ultrasound, arteriography).
  • Patients affected are usually males over 50 years of age, smokers, with a history of diabetes mellitus, arterial hypertension (AHT), chronic obstructive pulmonary disease (COPD), etc.
  • Diagnosis is based on clinical symptoms, outstandingly lumboabdominal pain, and the finding of a beating abdominal tumor, as well as signs of a renal failure.

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  • (PMID = 16724713.001).
  • [ISSN] 0004-0614
  • [Journal-full-title] Archivos españoles de urología
  • [ISO-abbreviation] Arch. Esp. Urol.
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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89. Hirayama Y, Kubota M, Imamura M, Imai C, Okuyama N, Tsukada M, Kobayashi K, Sato K, Takachi T, Iwavuchi H, Uchiyama M: A 2-year-old boy with a stage III yolk sac tumor occurring in an intra-abdominal retained testis. J Pediatr Surg; 2009 Dec;44(12):2395-8
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  • [Title] A 2-year-old boy with a stage III yolk sac tumor occurring in an intra-abdominal retained testis.
  • We, herein, report the case of a 2-year-old boy who presented with a huge yolk sac tumor with retroperitoneal lymph nodes metastasis that originated in a left intra-abdominal undescended testis.
  • Computed tomography and magnetic resonance imaging showed a huge round tumor connecting to the left retroperitoneal lymph nodes with metastasis extending from the left pelvic region to the left renal hilum.
  • The right abdominal tumor appeared to be a giant testis that had strangulated at the neck of the cord.
  • The tumor had ruptured at the side of the left pelvic lymph node metastasis, and a yolk sac tumor was diagnosed from a histologic analysis of the resected specimens.
  • Postoperative PEB chemotherapy was effective, and a complete surgical resection of the tumor was performed 3 months after the initial laparotomy.
  • The pathologic findings showed fibrous tissue without any tumor cells.
  • This case might be a coincidental association of a yolk sac tumor occurring in an undescended testis, which thus caused a delay in making an accurate diagnosis.
  • [MeSH-major] Cryptorchidism / diagnosis. Endodermal Sinus Tumor / diagnosis. Testicular Neoplasms / diagnosis
  • [MeSH-minor] CA-125 Antigen / blood. Child, Preschool. Humans. Lymphatic Metastasis / diagnosis. Lymphatic Metastasis / pathology. Magnetic Resonance Imaging. Male. Neoplasm Staging. Preoperative Care. Retroperitoneal Neoplasms / secondary. Testis / pathology. Testis / surgery. Tomography, X-Ray Computed. alpha-Fetoproteins / analysis

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  • (PMID = 20006035.001).
  • [ISSN] 1531-5037
  • [Journal-full-title] Journal of pediatric surgery
  • [ISO-abbreviation] J. Pediatr. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / CA-125 Antigen; 0 / alpha-Fetoproteins
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90. Semczuk A, Skorupski P, Olcha P, Skomra D, Rechberger T, Gogacz M: Giant uterine leiomyomas causing bilateral hydronephrosis coexisting with endometrial cancer in polyp: a case study. Eur J Gynaecol Oncol; 2009;30(3):344-6
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  • A 50-year-old woman was admitted due to bilateral hydronephrosis caused by monstrous abdominal tumor to the IInd Department of Gynecology, Lublin Medical University, Lublin, Poland.
  • Pelvic examination revealed a huge, rough tumor, originating from the uterus.
  • Total abdominal hysterectomy with bilateral salpingo-oophorectomy was performed, and a giant uterus weighing 15.2 kg and measuring 35 x 29 x 18 cm was removed.
  • [MeSH-major] Endometrial Neoplasms / pathology. Hydronephrosis / etiology. Leiomyoma / pathology. Neoplasms, Multiple Primary / pathology. Polyps / pathology. Uterine Neoplasms / pathology

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  • (PMID = 19697639.001).
  • [ISSN] 0392-2936
  • [Journal-full-title] European journal of gynaecological oncology
  • [ISO-abbreviation] Eur. J. Gynaecol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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91. Padovani L, Huchet A, Claude L, Bernier V, Quetin P, Mahe M, Laprie A, Kerr C, Bondiau PY, Delarue A, Coze C, Gibon D, Barteau C, Maire JP, Carrie C, Muracciole X: Inter-clinician variability in making dosimetric decisions in pediatric treatment: a balance between efficacy and late effects. Radiother Oncol; 2009 Nov;93(2):372-6
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  • PURPOSE: To investigate variability of clinical target volume (CTV) delineation and deviations according to doses delivered in normal tissue for abdominal tumor irradiation in children.
  • [MeSH-major] Neoplasms / radiotherapy

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  • (PMID = 19647884.001).
  • [ISSN] 1879-0887
  • [Journal-full-title] Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
  • [ISO-abbreviation] Radiother Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Ireland
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92. Dill AL, Ifa DR, Manicke NE, Ouyang Z, Cooks RG: Mass spectrometric imaging of lipids using desorption electrospray ionization. J Chromatogr B Analyt Technol Biomed Life Sci; 2009 Sep 15;877(26):2883-9

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  • Lipids play important biological roles and differences in lipid compositions have been seen in diseases such as cancer and Alzheimer's disease.
  • DESI-MS has been used to image a variety of tissue samples including human liver adenocarcinoma, rat brain, human breast tissue and canine abdominal tumor tissue.

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  • (PMID = 19150258.001).
  • [ISSN] 1873-376X
  • [Journal-full-title] Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
  • [ISO-abbreviation] J. Chromatogr. B Analyt. Technol. Biomed. Life Sci.
  • [Language] ENG
  • [Grant] United States / NIGMS NIH HHS / GM / GM058008-07; United States / NIGMS NIH HHS / GM / R01 GM058008; United States / NIGMS NIH HHS / GM / 5R01 GM58008-07; United States / NIGMS NIH HHS / GM / R01 GM058008-07
  • [Publication-type] Evaluation Studies; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
  • [Publication-country] Netherlands
  • [Chemical-registry-number] 0 / Lipids
  • [Other-IDs] NLM/ NIHMS227068; NLM/ PMC2921711
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93. Yamaguchi T, Takahashi H, Kagawa R, Takeda R, Sakata S, Yamamoto M, Nishizaki D, Takamatsu T, Iwasa Y: Successfully-treated mesenteric non-Hodgkin's lymphoma involving hepatic mass--a case report. Gan To Kagaku Ryoho; 2007 May;34(5):783-7
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

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  • A 77-year-old man was referred to our hospital because of a right lower abdominal tumor.
  • Abdominal computed tomography showed a mass in the mesenterium at the ileocoecal region and multiple mass in the liver.
  • With the diagnosis of a mesenteric tumor with liver metastases, a laparotomy was performed.
  • After the 8th course of such chemotherapy, he was confirmed to have achieved a complete remission by abdominal computed tomography and Gallium scintigram.The Stage IV mesenteric diffuse large B-cell lymphoma involving the liver seems to be an indication for combination therapy of surgical resection and multiagent chemotherapy.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Liver Neoplasms / pathology. Lymphoma, B-Cell / surgery. Lymphoma, Large B-Cell, Diffuse / surgery. Mesentery. Peritoneal Neoplasms / surgery

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  • (PMID = 17496458.001).
  • [ISSN] 0385-0684
  • [Journal-full-title] Gan to kagaku ryoho. Cancer & chemotherapy
  • [ISO-abbreviation] Gan To Kagaku Ryoho
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 5J49Q6B70F / Vincristine; 80168379AG / Doxorubicin; 8N3DW7272P / Cyclophosphamide; 9PHQ9Y1OLM / Prednisolone; VAP-cyclo protocol
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94. Hirai K, Kita K, Mikata K, Fujikawa N, Kitami K: [Giant seminoma in abdominal retention of the testis manifested with unilateral leg pain: a case report]. Hinyokika Kiyo; 2005 Jul;51(7):471-4
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  • [Title] [Giant seminoma in abdominal retention of the testis manifested with unilateral leg pain: a case report].
  • Ultrasonography revealed reduced blood flow to the tibial artery, which suggested a vascular disease like arteriosclerosis obliterans.
  • Enhanced computed tomography (CT) revealed a huge abdominal tumor and a 3-dimensional CT scan showed a feeding artery from the left renal artery to the huge tumor.
  • Surgical exploration revealed a giant tumor with clouded ascites in the abdominal cavity containing class V cells revealed by cytological examination.
  • The tumor was easily resected.
  • The histological finding was pure seminoma invaded to peritoneum.
  • His leg pain was relieved after the tumor resection.
  • [MeSH-major] Cryptorchidism / complications. Leg. Pain / etiology. Seminoma / complications. Testicular Neoplasms / complications

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  • (PMID = 16119813.001).
  • [ISSN] 0018-1994
  • [Journal-full-title] Hinyokika kiyo. Acta urologica Japonica
  • [ISO-abbreviation] Hinyokika Kiyo
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
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95. Liu HL, McDannold N, Hynynen K: Focal beam distortion and treatment planning in abdominal focused ultrasound surgery. Med Phys; 2005 May;32(5):1270-80
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  • [Title] Focal beam distortion and treatment planning in abdominal focused ultrasound surgery.
  • It is possible that some of this variation is due to abdominal tissue inhomogeneity, which might be causing focal beam distortion, and might largely decrease the focusing ability in deep-seated tissues.
  • Abdominal MR data from four uterine fibroid patients were obtained to reconstruct the three-dimensional meshes of interfaces used in simulations, and one patient was selected to perform the analysis of key parameters in focused ultrasound surgery.
  • This study may offer important implications and information for treatment planning toward optimizing focused ultrasound surgery in uterine fibroid or other abdominal tumor treatments.
  • [MeSH-major] Abdomen / physiopathology. Abdomen / radiation effects. Leiomyoma / therapy. Models, Biological. Radiometry / methods. Therapy, Computer-Assisted / methods. Ultrasonic Therapy / methods. Uterine Neoplasms / therapy

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  • (PMID = 15984679.001).
  • [ISSN] 0094-2405
  • [Journal-full-title] Medical physics
  • [ISO-abbreviation] Med Phys
  • [Language] eng
  • [Publication-type] Clinical Trial; Comparative Study; Journal Article; Validation Studies
  • [Publication-country] United States
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96. Ramírez-Bollas J, Padilla-Rosciano A, Romero-Y Huesca A, Lavín-Lozano AJ, Medina-Castro JM, Dubón-García E, Turcios-Cadenas ER: [Maffucci's syndrome. Case reports and literature review]. Cir Cir; 2005 May-Jun;73(3):217-21

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Transliterated title] Síndrome de Maffucci. Informe de dos pacientes y revisión de la literatura.
  • Maffucci syndrome is a rare, congenital disease, which is associated with the appearance of multiple enchondromas (possibility of malignant transformation in 20 to 100%), soft tissue hemangiomas and other mesenchymatous injuries.
  • The patient had a history of subcutaneous abdominal tumor, exostosis, nodules and nodule in right breast.
  • Upon examination, a tumor was found in the right breast, exostosis of right tibia, injury to the right wrist and left thyroid nodule.
  • A diagnosis was made of Marffucci syndrome associated with mesenchymatous tumors.
  • [MeSH-minor] Adult. Bone Neoplasms / etiology. Bone Neoplasms / radiography. Chondrosarcoma / etiology. Chondrosarcoma / radiography. Female. Humans. Prognosis. Tomography, X-Ray Computed

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  • (PMID = 16091163.001).
  • [ISSN] 0009-7411
  • [Journal-full-title] Cirugía y cirujanos
  • [ISO-abbreviation] Cir Cir
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Mexico
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97. Kawate S, Takeyoshi I, Ikota H, Numaga Y, Sunose Y, Morishita Y: Endometrioid adenocarcinoma arising from endometriosis of the mesenterium of the sigmoid colon. Jpn J Clin Oncol; 2005 Mar;35(3):154-7
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  • This report presents a case of endometrioid adenocarcinoma arising from endometriosis of the mesenterium of the sigmoid colon following total abdominal hysterectomy and bilateral salpingo-oophorectomy for leiomyoma of the uterus and infiltrating pelvic endometriosis, and hormone replacement therapy.
  • A 62-year-old woman presented with an abdominal tumor.
  • Based on the diagnosis of mesocolonic tumor, sigmoidectomy with lymph node resection was performed.
  • The tumor cells were immunopositive for cytokeratin 7, but negative for cytokeratin 20, and the tumor was histologically diagnosed as endometrioid adenocarcinoma of the mesocolon.
  • The patient had been receiving high-dose unopposed estrogens for 14 years after a total abdominal hysterectomy and bilateral salpingo-oophorectomy.
  • Physicians should recognize that endometriosis-associated neoplasms are able to cause symptoms or signs such as abdominal and/or pelvic pain, pelvic mass, and vaginal bleeding, especially if the patient has been treated with hormone replacement therapy.
  • It is important to recognize the possibility of tumors arising from endometriosis when evaluating intestinal or mesenteric neoplasms in women, even in the patient who has previously undergone total abdominal hysterectomy and bilateral salpingo-oophorectomy, particularly if the patient has a history of endometriosis and has received hormone replacement therapy.
  • [MeSH-major] Carcinoma, Endometrioid / etiology. Endometriosis / pathology. Sigmoid Diseases / pathology. Sigmoid Neoplasms / etiology
  • [MeSH-minor] Cell Transformation, Neoplastic / pathology. Colon, Sigmoid / blood supply. Estrogen Replacement Therapy / adverse effects. Fallopian Tubes / surgery. Female. Humans. Hysterectomy. Leiomyoma / surgery. Lymph Node Excision. Mesentery / pathology. Middle Aged. Ovariectomy. Postoperative Period. Uterine Neoplasms / surgery

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  • (PMID = 15741306.001).
  • [ISSN] 0368-2811
  • [Journal-full-title] Japanese journal of clinical oncology
  • [ISO-abbreviation] Jpn. J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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98. Tsujikawa T, Saitoh Y, Andoh A, Imaeda H, Hata K, Minematsu H, Senoh K, Hayafuji K, Ogawa A, Nakahara T, Sasaki M, Fujiyama Y: Novel single-balloon enteroscopy for diagnosis and treatment of the small intestine: preliminary experiences. Endoscopy; 2008 Jan;40(1):11-5
ClinicalTrials.gov. clinical trials - ClinicalTrials.gov .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The indications for the examination were suspected mid-gastrointestinal bleeding (n = 12), Crohn's disease (n = 17), abdominal pain (n = 8), and abdominal tumor (n = 4).
  • Therefore, SBE may be a useful diagnostic and therapeutic tool in addition to DBE for investigating suspected small bowel disease.
  • [MeSH-minor] Abdominal Neoplasms / diagnosis. Abdominal Neoplasms / therapy. Abdominal Pain / diagnosis. Abdominal Pain / therapy. Adult. Aged. Aged, 80 and over. Cohort Studies. Crohn Disease / diagnosis. Crohn Disease / therapy. Equipment Design. Equipment Safety. Female. Gastrointestinal Hemorrhage / diagnosis. Gastrointestinal Hemorrhage / therapy. Humans. Japan. Male. Middle Aged. Reproducibility of Results. Risk Assessment. Sensitivity and Specificity. Treatment Outcome

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  • [CommentIn] Endoscopy. 2008 Jun;40(6):537; author reply 539 [18543140.001]
  • [CommentIn] Endoscopy. 2008 Nov;40(11):961-2; author reply 962 [19009491.001]
  • [CommentIn] Endoscopy. 2008 Jun;40(6):538; author reply 539 [18543141.001]
  • (PMID = 18058613.001).
  • [ISSN] 1438-8812
  • [Journal-full-title] Endoscopy
  • [ISO-abbreviation] Endoscopy
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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99. Vik TA, Pfluger T, Kadota R, Castel V, Tulchinsky M, Farto JC, Heiba S, Serafini A, Tumeh S, Khutoryansky N, Jacobson AF: (123)I-mIBG scintigraphy in patients with known or suspected neuroblastoma: Results from a prospective multicenter trial. Pediatr Blood Cancer; 2009 Jul;52(7):784-90
MedlinePlus Health Information. consumer health - Neuroblastoma.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • PROCEDURE: One hundred patients (mean age 4.7 years) were enrolled, 86 with a previous diagnosis of neuroblastoma, 13 with suspected disease based upon symptoms, imaging findings, and elevated catecholamines, and one adult with an abdominal tumor thought to be of neuroendocrine origin.
  • SPECT imaging of the thorax/abdomen/pelvis was performed in 51 patients.
  • Disease status was confirmed by histopathology, imaging results, catecholamine measurements, and follow-up.
  • RESULTS: Sixty-four patients had active disease, 30 were without disease, and 6 were judged indeterminate because of insufficient confirmatory data. (123)I-mIBG scintigraphy had a sensitivity of 88% (56/64) and specificity of 83% (25/30).
  • Most false-negative interpretations were in patients with minimal residual disease (n = 4), while false-positive interpretations generally involved atypical adrenal or other physiological uptake (n = 4).

  • Genetic Alliance. consumer health - Neuroblastoma.
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  • [Copyright] (c) 2009 Wiley-Liss, Inc.
  • (PMID = 19185008.001).
  • [ISSN] 1545-5017
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Publication-type] Clinical Trial, Phase III; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Iodine Radioisotopes; 0 / Radiopharmaceuticals; 35MRW7B4AD / 3-Iodobenzylguanidine
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100. Ramírez-Ortega MA, Villegas-Romero J, Márquez-Díaz A, Gómez-Díaz A: [A cystic mesenteric lymphangioma presented at the colon sigmoid. Case report]. Rev Med Inst Mex Seguro Soc; 2010 Sep-Oct;48(5):557-62
Genetic Alliance. consumer health - Lymphangioma.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Transliterated title] Linfangioma quístico de mesenterio en colon sigmoides. Informe de un caso.
  • BACKGROUND: Cystic lymphangioma of the mesentery is an uncommon tumor; its incidence is 1:160,000.
  • CLINICAL CASE: Female 25 years, attending consultation with a clinical picture suggestive of right ovarian cyst and increased abdominal perimeter.
  • On physical examination abdominal painful tumor was identified, with deep palpation and mobilization.
  • Abdominal ultrasound findings suggested giant right ovarian cyst.
  • CONCLUSIONS: Cystic lymphangioma of the mesentery is a benign abdominal tumor, which occurs frequently in children but in adults is rare.
  • [MeSH-major] Lymphangioma, Cystic. Mesentery. Neoplasms, Multiple Primary. Peritoneal Neoplasms. Sigmoid Neoplasms

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  • (PMID = 21205508.001).
  • [ISSN] 0443-5117
  • [Journal-full-title] Revista médica del Instituto Mexicano del Seguro Social
  • [ISO-abbreviation] Rev Med Inst Mex Seguro Soc
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Mexico
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