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1. Refaat MM, Idriss SZ, Blaszkowsky LS: Case report: an unusual case of adrenal neuroblastoma in pregnancy. Oncologist; 2008 Feb;13(2):152-6
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  • [Title] Case report: an unusual case of adrenal neuroblastoma in pregnancy.
  • Neuroblastomas are the fourth most common malignancy of childhood and account for most adrenal tumors in children.
  • We present herein an extremely rare case of adrenal neuroblastoma occurring in a 25-year-old woman during her first trimester of pregnancy.
  • Adult adrenal neuroblastoma is an uncommon malignancy and, to our knowledge, there was no case of this tumor occurring in pregnancy ever described in the English literature.
  • The case presentation is followed by a general discussion with an emphasis on the diagnosis, treatment, and follow-up of neuroblastoma and its association with pregnancy.
  • [MeSH-major] Adrenal Gland Neoplasms / diagnosis. Adrenalectomy. Neuroblastoma / diagnosis. Pregnancy Complications, Neoplastic / diagnosis
  • [MeSH-minor] Abortion, Spontaneous / etiology. Adult. Chorioamnionitis / etiology. Female. Humans. Neoplasm Staging. Pregnancy. Pregnancy Trimester, First. Risk Factors


2. Miwa Y, Uchida K, Nakayama H, Asaki N: Neuroblastoma of the adrenal gland in a ferret. J Vet Med Sci; 2010 Sep;72(9):1229-32
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  • [Title] Neuroblastoma of the adrenal gland in a ferret.
  • The excised mass was histologically diagnosed as a medullary tumor of the adrenal gland, and some neoplastic cells were beta III-tubulin-, doublecortin- and neurofilament-positive.
  • Based on these findings, the tumor was considered to be a neuroblastoma.

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  • (PMID = 20431253.001).
  • [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
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3. Jacob ES, Varghese RG, Toi PC, Bhaskaran R, Rai R: Congenital neuroblastoma with liver metastasis presenting with Hashimoto Pritzker disease. Indian J Pathol Microbiol; 2009 Jul-Sep;52(3):374-6
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  • [Title] Congenital neuroblastoma with liver metastasis presenting with Hashimoto Pritzker disease.
  • She was earlier diagnosed to have neuroblastoma of the adrenal gland which had metastasized to the liver.
  • [MeSH-major] Infant, Newborn, Diseases / diagnosis. Infant, Newborn, Diseases / pathology. Liver Neoplasms / diagnosis. Liver Neoplasms / secondary. Neuroblastoma / diagnosis. Neuroblastoma / pathology
  • [MeSH-minor] Adrenal Gland Neoplasms / pathology. Adrenal Glands / pathology. Antigens, CD / analysis. Antigens, Differentiation, Myelomonocytic / analysis. Female. Histocytochemistry. Humans. Infant. Infant, Newborn. Pregnancy. Skin Neoplasms / diagnosis. Skin Neoplasms / pathology. Skin Neoplasms / secondary. Young Adult


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4. Raveenthiran V, Cenita S, Viswanathan P: Stabler's sign revisited in a spontaneously ruptured neuroblastoma of the newborn. Am J Perinatol; 2008 Jan;25(1):17-20
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  • [Title] Stabler's sign revisited in a spontaneously ruptured neuroblastoma of the newborn.
  • Spontaneous adrenal hemorrhage is the most common cause of nontraumatic parietal ecchymosis sign in neonates.
  • We report the sign for the first time in a case of spontaneously ruptured adrenal neuroblastoma of newborn.
  • Perinatal physicians need to be aware of this unusual presentation of neonatal neuroblastoma.
  • [MeSH-major] Adrenal Gland Neoplasms / pathology. Ecchymosis / etiology. Neuroblastoma / pathology

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  • (PMID = 18050035.001).
  • [ISSN] 0735-1631
  • [Journal-full-title] American journal of perinatology
  • [ISO-abbreviation] Am J Perinatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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5. Meersman A, Wojciechowski M, Vaneerdeweg W, Jorens P, Michiels E, Ramet J: Acute retroperitoneal hemorrhage and shock as presenting signs of neuroblastoma in an infant. Pediatr Emerg Care; 2008 Jan;24(1):37-8
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  • [Title] Acute retroperitoneal hemorrhage and shock as presenting signs of neuroblastoma in an infant.
  • Adrenal hemorrhage after the neonatal period is rare.
  • Spontaneous bleeding within an adrenal neuroblastoma has been described, but acute massive hemorrhage is exceptional.
  • We describe a case of neuroblastoma of the adrenal gland presenting with acute life-threatening abdominal hemorrhage.
  • [MeSH-major] Adrenal Gland Neoplasms / diagnosis. Hemoperitoneum / diagnosis. Neuroblastoma / diagnosis. Shock, Hemorrhagic / diagnosis
  • [MeSH-minor] Acute Disease. Diagnosis, Differential. Emergency Service, Hospital. Follow-Up Studies. Humans. Infant. Laparotomy / methods. Lymphatic Metastasis. Male. Risk Assessment. Rupture, Spontaneous. Tomography, X-Ray Computed. Treatment Outcome. Wilms Tumor / diagnosis

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  • (PMID = 18212608.001).
  • [ISSN] 1535-1815
  • [Journal-full-title] Pediatric emergency care
  • [ISO-abbreviation] Pediatr Emerg Care
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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6. Araujo Júnior E, Sanchez Ayub E, Costa Santos EM, Moraes DJ, Rodrigues Pires C, Filho Sebastião MZ: [Prenatal ultrasound diagnosis of adrenal neuroblastoma]. Ginecol Obstet Mex; 2005 Aug;73(8):451-5
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  • [Title] [Prenatal ultrasound diagnosis of adrenal neuroblastoma].
  • [Transliterated title] Diagnóstico prenatal ultrasonográfico de neuroblastoma adrenal.
  • Neuroblastoma is the most frequent solid malignant tumor in the neonatal period; however, its diagnosis is very difficult in the prenatal one.
  • The antenatal ultrasound diagnosis is possible by finding a mixed mass in the adrenal gland.
  • We report a case of a bilateral adrenal neuroblastoma diagnosed by antenatal ultrasonography at the 29th week of gestation.
  • [MeSH-major] Adrenal Gland Neoplasms / ultrasonography. Fetal Diseases / ultrasonography. Neuroblastoma / ultrasonography. Ultrasonography, Prenatal


7. Otmani N, Khattab M: Metastatic neuroblastoma to the mandible in a 3-year-old boy: a case report. Med Oral Patol Oral Cir Bucal; 2007 May;12(3):E201-4
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  • [Title] Metastatic neuroblastoma to the mandible in a 3-year-old boy: a case report.
  • Although neuroblastoma is a relatively common malignancy of childhood and its dissemination to distant organs is often seen, metastasis to the mandible is rare.
  • A 3-year-old boy which a mandibular soft tissue mass was the initial presenting symptom of disseminated neuroblastoma is reported.
  • The results of biopsy were inconclusive and the differential diagnosis from the imaging studies included lymphoma, soft tissue sarcoma, and osteosarcoma.
  • A metastatic work-up disclosed neuroblastoma of the adrenal gland origin with osseous and bone marrow metastases.
  • This case illustrates that neuroblastoma at a young age, with bone metastases and bone marrow involvement are predictive of the poor outcome of the disease.
  • Therefore, detecting early stage metastasis is one of the essential factors for improving treatment of neuroblastoma patients.
  • [MeSH-major] Mandibular Neoplasms / secondary. Neuroblastoma / secondary
  • [MeSH-minor] Adrenal Gland Neoplasms / pathology. Child, Preschool. Fatal Outcome. Humans. Male. Neoplasm Staging / standards

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  • (PMID = 17468714.001).
  • [ISSN] 1698-6946
  • [Journal-full-title] Medicina oral, patología oral y cirugía bucal
  • [ISO-abbreviation] Med Oral Patol Oral Cir Bucal
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Spain
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8. Genc H, Haciyanli M, Haciyanli SG, Gelal F, Avci Uçarsoy A, Dag F: An adult adrenal neuroblastoma: a case report. Acta Chir Belg; 2005 Nov-Dec;105(6):673-6
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  • [Title] An adult adrenal neuroblastoma: a case report.
  • Neuroblastoma of the adrenal gland is an extremely rare tumour in adulthood although it is one of the most common malignancies in childhood.
  • In this report, we present a 52-year-old man who had a left adrenal mass on preoperative imaging.
  • The histopathological examination of the specimen revealed the diagnosis of neuroblastoma.
  • He had no metastatic disease at the time of diagnosis and received chemotherapy after the operation.
  • Although neuroblastoma of adrenal gland is rare in adulthood, it should be considered in the differential diagnosis for patients with adrenal masses.
  • [MeSH-major] Adrenal Gland Neoplasms / diagnosis. Neuroblastoma / diagnosis

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  • (PMID = 16438086.001).
  • [ISSN] 0001-5458
  • [Journal-full-title] Acta chirurgica Belgica
  • [ISO-abbreviation] Acta Chir. Belg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Belgium
  • [Chemical-registry-number] 5001-33-2 / Metanephrine; 55-10-7 / Vanilmandelic Acid
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9. Hattori Y, Kanamoto N, Kawano K, Iwakura H, Sone M, Miura M, Yasoda A, Tamura N, Arai H, Akamizu T, Nakao K, Maitani Y: Molecular characterization of tumors from a transgenic mouse adrenal tumor model: comparison with human pheochromocytoma. Int J Oncol; 2010 Sep;37(3):695-705
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  • [Title] Molecular characterization of tumors from a transgenic mouse adrenal tumor model: comparison with human pheochromocytoma.
  • Adrenal neuroblastoma and pheochromocytoma have the same embryonic origin from neural crest cells and mainly arise from the adrenal medulla.
  • Recently, transgenic mice exhibiting tumors in the bilateral adrenal medulla by the expression of SV40 T-antigen were developed.
  • In this study, we investigated mRNA expression in adrenal tumors of transgenic mice and compared them with human pheochromocytoma by DNA microarray analysis.
  • To compare mouse adrenal tumors and human pheochromacytoma, we found that the expressions of noradrenergic neuron-related genes, including dopa decarboxylase, phenylethanolamine-N-methyltransferase and chromogranin B, were up-regulated in humans but not in mice; however, the expression of neuroblastoma-related genes, including Mycn, paired-like homeobox 2b, gamma-aminobutyric acid A receptor beta3 subunit, islet 1 and kinesin family member 1A, was up-regulated in both species.
  • From the gene expression profiles, the characterization of mouse adrenal tumor, may be similar to that of human adrenal neuroblastoma rather than pheochromacytomas.
  • This mouse model would be a useful tool for the development of anti-cancer drugs and for understanding the etiology of adrenal neuroblastoma.
  • [MeSH-major] Adrenal Gland Neoplasms / genetics. Pheochromocytoma / genetics


10. Krug P, Schleiermacher G, Michon J, Valteau-Couanet D, Brisse H, Peuchmaur M, Sarnacki S, Martelli H, Desguerre I, Tardieu M: Opsoclonus-myoclonus in children associated or not with neuroblastoma. Eur J Paediatr Neurol; 2010 Sep;14(5):400-9
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  • [Title] Opsoclonus-myoclonus in children associated or not with neuroblastoma.
  • OBJECTIVE: To compare the clinical data at diagnosis, treatment and neurological outcome in 34 children with opsoclonus-myoclonus syndrome (OMS) associated with a detected neuroblastoma or not.
  • RESULTS: Twenty-two patients had OMS associated with a neuroblastoma.
  • Twelve children had OMS without a detected neuroblastoma.
  • In the 27 OMS patients with or without neuroblastoma whose follow up was greater than two years, the neurological outcome was evaluated: 59.3% had neurological sequelae, including motor, praxic and/or language sequelae (n=9), persistent ataxia (n=6) and moderate motor deficit (n=3).
  • CONCLUSION: Our retrospective study provides further evidence that OMS with or without a detected neuroblastoma is the same disease, whose major challenges are the neurological sequelae.
  • An international collaboration is required to improve the knowledge about OMS, the treatment and the outcome in this rare disorder.
  • [MeSH-major] Neuroblastoma / complications. Opsoclonus-Myoclonus Syndrome / physiopathology
  • [MeSH-minor] Adrenal Cortex Hormones / therapeutic use. Child, Preschool. Female. Humans. Infant. Male. Retrospective Studies

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  • [Copyright] Copyright (c) 2009 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.
  • (PMID = 20110181.001).
  • [ISSN] 1532-2130
  • [Journal-full-title] European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
  • [ISO-abbreviation] Eur. J. Paediatr. Neurol.
  • [Language] eng
  • [Publication-type] Journal Article; Multicenter Study
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Adrenal Cortex Hormones
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11. Pagès PM, Dufour C, Fasola S, Michon J, Boutard P, Gentet JC, Hartmann O: Bilateral adrenal neuroblastoma. Pediatr Blood Cancer; 2009 Feb;52(2):196-202
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  • [Title] Bilateral adrenal neuroblastoma.
  • BACKGROUND: Bilateral adrenal neuroblastoma is extremely rare.
  • PROCEDURES: We retrospectively identified and reviewed 15 cases of bilateral adrenal neuroblastoma, treated between 1988 and 2004, by the French Society of Pediatric Oncology.
  • RESULTS: Median age at diagnosis was 4 months in our cohort whereas it was 3 months in the literature.
  • Ten out of 15 patients in our cohort and 18/39 cases in the literature were classified as stage 4S according to the International Neuroblastoma Staging System (INSS).
  • The incidence of stage 4S was significantly higher than that described in other neuroblastoma cohorts (P = 10(-4)).
  • In our series, bilateral neuroblastoma was neither associated with familial cases nor with any risk factors.
  • CONCLUSIONS: The majority of bilateral neuroblastoma carry a favorable prognosis.
  • Exceptional cases exhibiting risk factors, such as amplified MYCN, are comparable to high-risk unilateral neuroblastoma cases with the same poor prognostic features.
  • The therapeutic strategy could be similar to that used against unilateral neuroblastoma, except for surgery.
  • However, the low incidence of relapse and the risk of adrenal failure if radical surgery is performed, argue against an aggressive surgical approach.
  • [MeSH-major] Adrenal Gland Neoplasms / epidemiology. Neuroblastoma / epidemiology

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  • [Copyright] (c) 2008 Wiley-Liss, Inc.
  • (PMID = 18951434.001).
  • [ISSN] 1545-5017
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Multicenter Study
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 0 / MYCN protein, human; 0 / Nuclear Proteins; 0 / Oncogene Proteins
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12. Pederiva F, Andres A, Sastre A, Alves J, Martinez L, Tovar JA: Bilateral adrenal neuroblastoma is different. Eur J Pediatr Surg; 2007 Dec;17(6):393-6
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  • [Title] Bilateral adrenal neuroblastoma is different.
  • BACKGROUND/AIMS: Bilateral adrenal neuroblastoma is rare and can be due to multifocal primary or contralateral metastasis.
  • The present study examines the clinical, biological and therapeutic features of bilateral adrenal neuroblastoma.
  • CONCLUSIONS: Bilateral adrenal neuroblastomas fit neither into stage 4 s nor into stage 4.
  • [MeSH-major] Adrenal Gland Neoplasms / diagnosis. Neuroblastoma / diagnosis
  • [MeSH-minor] Adrenalectomy / methods. Antineoplastic Agents / therapeutic use. Biopsy. Diagnosis, Differential. Fatal Outcome. Female. Follow-Up Studies. Humans. Infant. Infant, Newborn. Male. Retrospective Studies. Tomography, X-Ray Computed

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  • (PMID = 18072022.001).
  • [ISSN] 0939-7248
  • [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] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Antineoplastic Agents
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13. Johnston DL, Sweeney B, Halton JM: Bilateral adrenal neuroblastoma: stage V disease. J Pediatr Hematol Oncol; 2007 Sep;29(9):652-5
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  • [Title] Bilateral adrenal neuroblastoma: stage V disease.
  • Neuroblastoma frequently arises from the adrenal gland and has rarely been reported to arise synchronously in both adrenal glands.
  • The majority of reports of bilateral adrenal neuroblastoma are in children under the age of 1 year.
  • We present a case of bilateral adrenal neuroblastoma in an 8-year-old child.
  • This is the first report of bilateral disease in a child over the age of 1 year with stage IV neuroblastoma.
  • [MeSH-major] Adrenal Gland Neoplasms / diagnosis. Neuroblastoma / diagnosis
  • [MeSH-minor] Child. Fatal Outcome. Humans. Magnetic Resonance Imaging. Male. Neoplasm Staging

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  • [CommentIn] J Pediatr Hematol Oncol. 2008 May;30(5):408-9 [18458582.001]
  • (PMID = 17805045.001).
  • [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
  • [Publication-country] United States
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14. Wang J, Pei G, Yan J, Zhang G: Coexistence of a giant splenic hemangioma and multiple hepatic hemangiomas mimicking a left adrenal neuroblastoma accompanied with multifocal hepatic metastases: pyrite answer. J Pediatr Hematol Oncol; 2009 Dec;31(12):983-4
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  • [Title] Coexistence of a giant splenic hemangioma and multiple hepatic hemangiomas mimicking a left adrenal neuroblastoma accompanied with multifocal hepatic metastases: pyrite answer.
  • A 4-month girl presenting with a giant mass in left adrenal region and multiple hepatic nodules was hospitalized.
  • On the basis of computed tomography, ultrasound and epidemiology we preferred the diagnosis of a left adrenal neuroblastoma accompanied with multiple hepatic metastases preoperatively.
  • But postoperative diagnosis was hemangiomatosis characterized by synchronous presence of a giant splenic hemangioma and multiple hepatic hemangiomas.
  • We think that it is deservedly reported because of not only its rarity but also pitfalls of preoperative differential diagnosis and management principle.
  • [MeSH-major] Adrenal Gland Neoplasms / diagnosis. Hemangioma / pathology. Liver Neoplasms / pathology. Neoplasms, Second Primary / pathology. Neuroblastoma / diagnosis. Splenic Neoplasms / pathology
  • [MeSH-minor] Diagnosis, Differential. Female. Humans. Infant. Magnetic Resonance Imaging. Tomography, X-Ray Computed. Ultrasonography


15. Berrebi D, Lebras MN, Belarbi N, Couturier J, Fattet S, Faye A, Peuchmaur M, de Lagausie P: Bilateral adrenal neuroblastoma and nephroblastoma occurring synchronously in a child with Fanconi's anemia and VACTERL syndrome. J Pediatr Surg; 2006 Jan;41(1):e11-4
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  • [Title] Bilateral adrenal neuroblastoma and nephroblastoma occurring synchronously in a child with Fanconi's anemia and VACTERL syndrome.
  • Such association led quickly to the diagnosis of FA.
  • At age of 11 months, she developed simultaneously a renal tumor in a horseshoe kidney and bilateral adrenal tumors.
  • The left adrenal mass was removed, and partial nephrectomy was performed.
  • Histological analysis concluded to adrenal neuroblastoma and nephroblastoma.
  • [MeSH-major] Adrenal Gland Neoplasms / pathology. Fanconi Anemia / complications. Kidney Neoplasms / pathology. Neuroblastoma / pathology. Wilms Tumor / pathology


16. Janjanin N, Dumic M, Skrabic V, Kusec V, Grubic Z, Spehar Uroic A: Five patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (one with associated neuroblastoma) discovered in three generations of one family. Horm Res; 2007;67(3):111-6
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  • [Title] Five patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (one with associated neuroblastoma) discovered in three generations of one family.
  • CASE REPORT: We present 5 patients with congenital adrenal hyperplasia (CAH) due to 21-OHD belonging to the 3 generations of the same family (grandmother, parents and their 2 children).
  • The probands' mother, besides the nonclassical 21-OHD, also had neuroblastoma of the adrenal gland.
  • The occurrence of neuroblastoma with 21-OHD may support the hypothesis that an impairment in the synthesis and secretion of glucocorticoids may play role in the development and functioning of the adrenal medulla.
  • [MeSH-major] Adrenal Gland Neoplasms / complications. Adrenal Hyperplasia, Congenital / diagnosis. Neuroblastoma / complications. Steroid 21-Hydroxylase


17. Boyd DT, Hayeri MR, Kadom N: Parotid metastasis from adrenal neuroblastoma. Pediatr Radiol; 2010 Dec;40 Suppl 1:S113-5
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  • [Title] Parotid metastasis from adrenal neuroblastoma.
  • In contrast, salivary gland tumors are uncommon in children, accounting for only 1% of all pediatric neoplasms.
  • We present a case of a parotid metastasis from a neuroblastoma with in-depth description and discussion of its ultrasound (US), computed tomography (CT) and magnetic resonance imaging (MRI) appearances.
  • [MeSH-major] Adrenal Gland Neoplasms / diagnosis. Diagnostic Imaging / methods. Neuroblastoma / diagnosis. Neuroblastoma / secondary. Parotid Neoplasms / diagnosis. Parotid Neoplasms / secondary


18. Schalk E, Mohren M, Koenigsmann M, Buhtz P, Franke A, Jentsch-Ullrich K: Metastatic adrenal neuroblastoma in an adult. Onkologie; 2005 Jun;28(6-7):353-5
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  • [Title] Metastatic adrenal neuroblastoma in an adult.
  • BACKGROUND: Neuroblastoma (NB) is a common malignancy in children, but rarely occurs in adults.
  • In adults, abdomen/retroperitoneum are the primary sites and in children the adrenal gland.
  • Tumour resection revealed adrenal NB grade III.
  • Chemotherapy according to the paediatric German Neuroblastoma Trial (NB97) was started.
  • The patient died 9 months after diagnosis.
  • [MeSH-major] Adrenal Gland Neoplasms / pathology. Neuroblastoma / pathology. Neuroblastoma / secondary

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  • (PMID = 15933424.001).
  • [ISSN] 0378-584X
  • [Journal-full-title] Onkologie
  • [ISO-abbreviation] Onkologie
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Switzerland
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19. Chacko J, Karl S, Sen S, Eapen A, Mathai J: Bilateral cystic adrenal neuroblastoma with cystic metastasis in the liver. J Pediatr Surg; 2007 Aug;42(8):E11-3
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  • [Title] Bilateral cystic adrenal neuroblastoma with cystic metastasis in the liver.
  • Ultrasound and computerized tomography showed a large cystic lesion in the right adrenal, small cysts in the left adrenal, and multiple cystic liver metastases.
  • The right adrenal cyst, on excision, turned out to be a cystic neuroblastoma with hemorrhage.
  • On follow-up, the cysts in the left adrenal and the liver metastases are regressing.
  • [MeSH-major] Adrenal Gland Neoplasms / diagnosis. Liver Neoplasms / diagnosis. Neuroblastoma / diagnosis

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  • (PMID = 17706480.001).
  • [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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20. Alsultan A, Lovell MA, Hayes KL, Allshouse MJ, Garrington TP: Simultaneous occurrence of right adrenocortical tumor and left adrenal neuroblastoma in an infant with Beckwith-Wiedemann syndrome. Pediatr Blood Cancer; 2008 Nov;51(5):695-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Simultaneous occurrence of right adrenocortical tumor and left adrenal neuroblastoma in an infant with Beckwith-Wiedemann syndrome.
  • We present the case of an infant with BWS who has hypomethylation of LIT1 gene in the 11p15.5 chromosomal region and at 6 months of age presented with simultaneous occurrence of neuroblastoma arising from the left adrenal gland and a right adrenocortical tumor.
  • [MeSH-major] Adrenal Cortex Neoplasms / complications. Adrenal Gland Neoplasms / complications. Beckwith-Wiedemann Syndrome / complications. Neoplasms, Multiple Primary / complications. Neuroblastoma / complications


21. Tatekawa Y, Muraji T, Nishijima E, Yoshida M, Tsugawa C: Composite pheochromocytoma associated with adrenal neuroblastoma in an infant: a case report. J Pediatr Surg; 2006 Feb;41(2):443-5
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  • [Title] Composite pheochromocytoma associated with adrenal neuroblastoma in an infant: a case report.
  • Screening abdominal ultrasonography showed a 6-cm-sized mass in the left adrenal gland.
  • Metaiodobenzyl guanidine I 123 scintigram, abdominal computed tomography, and abdominal magnetic resonance imaging revealed only left adrenal tumor with no metastasis.
  • Left adrenalectomy was performed transperitoneally, and histopathological diagnosis was an adrenal composite pheochromocytoma associated with neuroblastoma.
  • Immunoreactivity for vimentin was positive in pheochromocytoma, which was negative in neuroblastoma.
  • [MeSH-major] Adrenal Gland Neoplasms / pathology. Neoplasms, Multiple Primary / pathology. Neuroblastoma / pathology. Pheochromocytoma / pathology


22. Patterson AR, Barker CS, Loukota RA, Spencer J: Ganglioneuroma of the mandible resulting from metastasis of neuroblastoma. Int J Oral Maxillofac Surg; 2009 Feb;38(2):196-8
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  • [Title] Ganglioneuroma of the mandible resulting from metastasis of neuroblastoma.
  • Neuroblastoma, ganglioneuroblastoma and ganglioneuroma are neuroblastic tumours derived from primordial neural crest tissue.
  • The authors report a rare presentation of a ganglioneuroma of the mandible arising from a metastasis of an adrenal neuroblastoma.
  • [MeSH-major] Adrenal Gland Neoplasms / pathology. Ganglioneuroblastoma / pathology. Ganglioneuroma / radiography. Mandibular Neoplasms / secondary. Neoplasms, Neuroepithelial / secondary. Neuroblastoma / secondary

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  • (PMID = 19019630.001).
  • [ISSN] 1399-0020
  • [Journal-full-title] International journal of oral and maxillofacial surgery
  • [ISO-abbreviation] Int J Oral Maxillofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
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23. Köksal Y, Varan A, Kale G, Tanyel FC, Büyükpamukçu M: Bilateral adrenal cystic neuroblastoma with hepatic and splenic involvement in a newborn. J Pediatr Hematol Oncol; 2005 Dec;27(12):670-1
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  • [Title] Bilateral adrenal cystic neuroblastoma with hepatic and splenic involvement in a newborn.
  • Bilateral cystic adrenal neuroblastoma is an unusual variant of neuroblastoma, and only two cases have been reported in the neonatal period until now.
  • The authors describe a newborn with splenic and hepatic involvement of bilateral adrenal cystic neuroblastoma.
  • [MeSH-major] Adrenal Gland Neoplasms / congenital. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Liver Neoplasms / secondary. Neuroblastoma / congenital. Splenic Neoplasms / secondary

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  • (PMID = 16344674.001).
  • [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
  • [Publication-country] United States
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24. Sherer DM, Dalloul M, Wagreich A, Sokolovski M, Duan H, Zinn H, Abulafia O: Prenatal sonographic findings of congenital adrenal cortical adenoma. J Ultrasound Med; 2008 Jul;27(7):1091-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Prenatal sonographic findings of congenital adrenal cortical adenoma.
  • The differential diagnosis of prenatally diagnosed adrenal masses includes neuroblastoma, adrenal hemorrhage, adrenal and cortical renal cysts, adrenal adenoma and carcinoma, subdiaphragmatic pulmonary sequestration, Beckwith-Wiedemann syndrome, duplication of the renal system, Wilms tumors, congenital mesoblastic nephroma, and mesenteric and enteric duplication cysts.
  • The worldwide annual incidence of childhood adrenal cortical neoplasms ranges between 0.3 and 0.38 per 1 million children younger than 15 years.
  • [MeSH-major] Adrenal Cortex Neoplasms / congenital. Adrenal Cortex Neoplasms / diagnosis. Adrenocortical Adenoma / congenital. Adrenocortical Adenoma / diagnosis. Ultrasonography, Prenatal / methods
  • [MeSH-minor] Adrenal Cortex / surgery. Adrenal Cortex / ultrasonography. Adult. Diagnosis, Differential. Female. Humans. Imaging, Three-Dimensional / methods. Infant, Newborn. Male. Pregnancy. Radiography, Abdominal / methods. Tomography, X-Ray Computed

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  • (PMID = 18577675.001).
  • [ISSN] 0278-4297
  • [Journal-full-title] Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine
  • [ISO-abbreviation] J Ultrasound Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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25. Seefelder C, Sparks JW, Chirnomas D, Diller L, Shamberger RC: Perioperative management of a child with severe hypertension from a catecholamine secreting neuroblastoma. Paediatr Anaesth; 2005 Jul;15(7):606-10
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Perioperative management of a child with severe hypertension from a catecholamine secreting neuroblastoma.
  • We report the perioperative management of a 5 year old child with stage III adrenal neuroblastoma who presented with malignant hypertension and high norepinephrine and dopamine levels.
  • [MeSH-major] Catecholamines / metabolism. Catecholamines / physiology. Hypertension / etiology. Hypertension / therapy. Kidney Neoplasms / complications. Kidney Neoplasms / metabolism. Neuroblastoma / complications. Neuroblastoma / metabolism


26. Miyagawa-Hayashino A, Sonobe M, Kubo T, Yoshizawa A, Date H, Manabe T: Non-specific interstitial pneumonia as a manifestation of graft-versus-host disease following pediatric allogeneic hematopoietic stem cell transplantation. Pathol Int; 2010 Feb;60(2):137-42
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  • Reported herein is a fibrosing non-specific interstitial pneumonia (NSIP) pattern together with BO in both lungs in an 8-year-old girl following a second allogeneic hematopoietic stem cell transplantation for relapsed neuroblastoma of adrenal origin.
  • [MeSH-minor] Adrenal Gland Neoplasms / pathology. Adrenal Gland Neoplasms / therapy. Bronchiolitis Obliterans / etiology. Bronchiolitis Obliterans / pathology. Child. Female. Humans. Lung Transplantation. Neoplasm Recurrence, Local / therapy. Neuroblastoma / pathology. Neuroblastoma / therapy. Transplantation, Homologous

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  • (PMID = 20398200.001).
  • [ISSN] 1440-1827
  • [Journal-full-title] Pathology international
  • [ISO-abbreviation] Pathol. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
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27. Auber F, Larroquet M, Bonnard A, Boudjemaa S, Landman-Parker J, Ducou Le Pointe H, Boccon-Gibod L, Lefebvre G, Uzan S, Hélardot P, Audry G: [Prenatal ultrasound diagnosis of neuroblastoma]. Gynecol Obstet Fertil; 2005 Apr;33(4):228-31
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Prenatal ultrasound diagnosis of neuroblastoma].
  • With the progress of foetal ultrasonography, diagnosis of foetal tumors can be made before birth.
  • We report five cases of prenatally detected neuroblastoma of the adrenal glands.
  • Diagnosis was made during the third trimester in all cases.
  • In each setting the tumor was a stage I neuroblastoma according to the Evans classification.
  • [MeSH-major] Adrenal Gland Neoplasms / ultrasonography. Fetal Diseases / ultrasonography. Neuroblastoma / ultrasonography. Ultrasonography, Prenatal


28. Gorman MP: Update on diagnosis, treatment, and prognosis in opsoclonus-myoclonus-ataxia syndrome. Curr Opin Pediatr; 2010 Dec;22(6):745-50
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Update on diagnosis, treatment, and prognosis in opsoclonus-myoclonus-ataxia syndrome.
  • PURPOSE OF REVIEW: Opsoclonus-myoclonus-ataxia syndrome (OMS) is a severe autoimmune central nervous system disorder, which predominantly affects young children and causes lifelong neurological disability.
  • RECENT FINDINGS: Appreciation of the spectrum of clinical presentations of OMS, awareness of common misdiagnoses, and utilization of diagnostic criteria may facilitate the timely diagnosis of OMS.
  • Approximately 50% of patients have an associated neuroblastoma, which may escape detection by traditional methods and require MRI or computed tomography of the torso for diagnosis.
  • SUMMARY: The diagnosis of OMS requires a high level of suspicion and a systematic approach for diagnostic testing, particularly for neuroblastoma.
  • [MeSH-minor] Adrenal Cortex Hormones / therapeutic use. Humans. Treatment Outcome


29. Pellkofer HL, Voltz R, Goebels N, Hohlfeld R, Dornmair K: Cross-reactive T-cell receptors in tumor and paraneoplastic target tissue. Arch Neurol; 2009 May;66(5):655-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: According to established criteria, paraneoplastic encephalomyelitis with adrenal neuroblastoma comprises a definite paraneoplastic neurologic syndrome.
  • Patient A 22-year-old woman having paraneoplastic encephalomyelitis with adrenal neuroblastoma.
  • MAIN OUTCOME MEASURES: We compared the T-cell receptor repertoires expressed in blood, cerebrospinal fluid, and neuroblastoma tumor tissue using complementary determining region 3 (CDR3) spectratyping and clone-specific polymerase chain reaction.
  • [MeSH-major] Adrenal Gland Neoplasms / immunology. Neuroblastoma / immunology. Paraneoplastic Syndromes, Nervous System / immunology. Receptors, Antigen, T-Cell / analysis
  • [MeSH-minor] Antigens, Neoplasm / analysis. Antigens, Neoplasm / classification. Biomarkers / analysis. Biomarkers / blood. Biomarkers / cerebrospinal fluid. Cell Lineage / immunology. Clone Cells / immunology. Cross Reactions / immunology. Female. Humans. Immunophenotyping. Lymphocyte Activation / immunology. Receptors, Antigen, T-Cell, alpha-beta / analysis. T-Lymphocyte Subsets / immunology. T-Lymphocytes / classification. T-Lymphocytes / immunology. Young Adult

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  • [CommentIn] Arch Neurol. 2009 Oct;66(10):1299-300; author reply 300 [19822792.001]
  • (PMID = 19433667.001).
  • [ISSN] 1538-3687
  • [Journal-full-title] Archives of neurology
  • [ISO-abbreviation] Arch. Neurol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, Neoplasm; 0 / Biomarkers; 0 / Receptors, Antigen, T-Cell; 0 / Receptors, Antigen, T-Cell, alpha-beta
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30. Rabah R, Weber R, Serhatkulu GK, Cao A, Dai H, Pandya A, Naik R, Auner G, Poulik J, Klein M: Diagnosis of neuroblastoma and ganglioneuroma using Raman spectroscopy. J Pediatr Surg; 2008 Jan;43(1):171-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Diagnosis of neuroblastoma and ganglioneuroma using Raman spectroscopy.
  • BACKGROUND: Raman spectroscopy has proven to be useful in studying premalignant and malignant lesions in adults.
  • This is the first report to evaluate Raman spectroscopy in the diagnosis and classification of neuroblastoma in children.
  • METHODS: A biopsy or resection of fresh tissue samples from normal adrenal glands, neuroblastomas, ganglioneuromas, nerve sheath tumors, and pheochromocytoma at our hospital were equally divided between routine histology and spectroscopic studies.
  • RESULTS: We collected 698 spectra from 16 neuroblastomas, 5 ganglioneuromas, 3 normal adrenal glands, 6 nerve sheath tumors, and 1 pheochromocytoma.
  • Raman spectroscopy differentiated between normal adrenal gland, and neuroblastoma and ganglioneuroma with 100% sensitivity and 100% specificity.
  • It was also able to differentiate neuroblastoma from nerve sheath tumors and pheochromocytoma with high sensitivity and specificity.
  • CONCLUSION: This technique can differentiate neuroblastoma from ganglioneuroma and other tumors.
  • [MeSH-major] Adrenal Gland Neoplasms / diagnosis. Ganglioneuroma / diagnosis. Neuroblastoma / diagnosis. Pheochromocytoma / diagnosis. Spectrum Analysis, Raman / methods
  • [MeSH-minor] Biopsy, Needle. Child. Child, Preschool. Diagnosis, Differential. Female. Humans. Immunohistochemistry. Infant. Male. Sampling Studies. Sensitivity and Specificity. Tissue Embedding


31. Tanaka M, Kato K, Gomi K, Matsumoto M, Kudo H, Shinkai M, Ohama Y, Kigasawa H, Tanaka Y: Perivascular epithelioid cell tumor with SFPQ/PSF-TFE3 gene fusion in a patient with advanced neuroblastoma. Am J Surg Pathol; 2009 Sep;33(9):1416-20
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Perivascular epithelioid cell tumor with SFPQ/PSF-TFE3 gene fusion in a patient with advanced neuroblastoma.
  • We report a case of perivascular epithelioid cell tumor (PEComa) with an SFPQ/PSF-TFE3 gene fusion in a 14-year-old girl treated for adrenal neuroblastoma for 4 years.
  • Imaging studies revealed a tumor in the wall of the sigmoid colon, which was radiologically different from the neuroblastoma, together with several inguinal and cervical lymph node metastases of the neuroblastoma.
  • [MeSH-major] Basic Helix-Loop-Helix Leucine Zipper Transcription Factors / genetics. Colonic Neoplasms / pathology. Neuroblastoma / secondary. Perivascular Epithelioid Cell Neoplasms / pathology

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  • (PMID = 19606011.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Basic Helix-Loop-Helix Leucine Zipper Transcription Factors; 0 / PTB-associated splicing factor; 0 / RNA-Binding Proteins; 0 / TFE3 protein, human
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32. Oguzkurt P, Ince E, Temiz A, Demir S, Akabolat F, Hicsonmez A: Prenatal diagnosis of a mass in the adrenal region that proved to be a teratoma. J Pediatr Hematol Oncol; 2009 May;31(5):350-1
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Prenatal diagnosis of a mass in the adrenal region that proved to be a teratoma.
  • Magnetic resonance imaging showed a 57 x 50 mm mass in the left adrenal region displacing the kidney inferiorly.
  • Prenatally detected suprarenal masses are likely to be neuroblastoma or adrenal hemorrhage, but may be rare benign lesions such as extralobar pulmonary sequestration, bronchogenic cyst, or renal dysplasia.
  • Although teratoma in the adrenal region is extremely rare, it should be included in the clinical and radiologic differential diagnosis of prenatally detected suprarenal masses.
  • Total excision of the mass for histologic diagnosis is indicated.
  • [MeSH-major] Adrenal Gland Neoplasms / congenital. Adrenal Gland Neoplasms / diagnosis. Teratoma / congenital. Teratoma / diagnosis. Ultrasonography, Prenatal
  • [MeSH-minor] Adrenalectomy. Biopsy. Diagnosis, Differential. Female. Humans. Infant. Magnetic Resonance Imaging. Male. Pregnancy

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  • (PMID = 19415017.001).
  • [ISSN] 1536-3678
  • [Journal-full-title] Journal of pediatric hematology/oncology
  • [ISO-abbreviation] J. Pediatr. Hematol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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33. Sorrentino S, Conte M, Nozza P, Granata C, Capra V, Avanzini S, Garaventa A: Simultaneous occurrence of pancreatoblastoma and neuroblastoma in a newborn with beckwith-wiedemann syndrome. J Pediatr Hematol Oncol; 2010 Jul;32(5):e207-9
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  • [Title] Simultaneous occurrence of pancreatoblastoma and neuroblastoma in a newborn with beckwith-wiedemann syndrome.
  • We report the case of a newborn with Beckwith-Wiedemann syndrome presenting the simultaneous occurrence of a cystic pancreatoblastoma and an adrenal neuroblastoma.
  • Surgery was required to treat the pancreatoblastoma, and a "wait and see" policy was adopted for the neuroblastoma, which spontaneously regressed within a few months.
  • [MeSH-major] Beckwith-Wiedemann Syndrome / etiology. Neoplasms, Multiple Primary / etiology. Neuroblastoma / etiology. Pancreatic Cyst / etiology. Pancreatic Neoplasms / etiology
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Humans. Infant, Newborn. Male. Pregnancy. Prognosis. Tomography, X-Ray Computed. Ultrasonography, Prenatal


34. Bähr A, Schulte-Vallentin M, Hasse J, Werner M, Jüttner E, Uhl M, Niemeyer C, Kontny U: [Extrathoracal pulmonary sequestration in the differential diagnosis of paravertebral tumors in the neonate]. Klin Padiatr; 2006 Jan-Feb;218(1):13-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Extrathoracal pulmonary sequestration in the differential diagnosis of paravertebral tumors in the neonate].
  • The most common differential diagnoses of these tumors are neuroblastoma, adrenal hemorrhage, schwannoma and germ cell tumors.
  • Hence, a biopsy procedure should be done for diagnosis of paravertebral masses.
  • [MeSH-major] Bronchopulmonary Sequestration / diagnosis. Neuroblastoma / congenital. Spinal Neoplasms / congenital. Thoracic Vertebrae. Ultrasonography, Prenatal
  • [MeSH-minor] Biopsy. Cesarean Section. Diagnosis, Differential. Humans. Lung / pathology. Lung / surgery. Magnetic Resonance Imaging. Male. Ultrasonography

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  • (PMID = 16432768.001).
  • [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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35. Avni FE, Massez A, Cassart M: Tumours of the fetal body: a review. Pediatr Radiol; 2009 Nov;39(11):1147-57
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Adrenal neuroblastoma is the commonest malignant tumour.
  • [MeSH-major] Fetal Diseases / diagnosis. Magnetic Resonance Imaging / methods. Neoplasms / congenital. Neoplasms / diagnosis. Prenatal Diagnosis / methods. Ultrasonography / methods


36. Bacchetta J, Douvillez B, Warin L, Girard S, Pagès MP, Rebaud P, Bertrand Y: [Blueberry Muffin Baby and spontaneous remission of neonatal leukaemia]. Arch Pediatr; 2008 Aug;15(8):1315-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Blueberry Muffin baby is a rare neonatal skin disorder.
  • We report on a newborn presenting with Blueberry Muffin syndrome and an adrenal mass which lead to the diagnosis of neuroblastoma.
  • Actually, it corresponded to an acute monoblastic leukaemia with an adrenal localization and a cerebrospinal fluid involvement.
  • [MeSH-minor] Diagnosis, Differential. Female. Follow-Up Studies. Humans. Infant. Infant, Newborn. Remission, Spontaneous. Time Factors

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  • (PMID = 18595669.001).
  • [ISSN] 0929-693X
  • [Journal-full-title] Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie
  • [ISO-abbreviation] Arch Pediatr
  • [Language] fre
  • [Publication-type] Case Reports; Comparative Study; English Abstract; Journal Article
  • [Publication-country] France
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37. Pianovski MA, Maluf EM, de Carvalho DS, Ribeiro RC, Rodriguez-Galindo C, Boffetta P, Zancanella P, Figueiredo BC: Mortality rate of adrenocortical tumors in children under 15 years of age in Curitiba, Brazil. Pediatr Blood Cancer; 2006 Jul;47(1):56-60
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Several reports refer to an increased frequency of adrenal cortex tumors (ACT) among children in Southern Brazil, yet all data have been derived from hospital-based registries.
  • PROCEDURE: We reviewed all death certificates that mentioned ACT or adrenal neuroblastoma (NB) and which were reported to the Paraná State Department of Health between 1998 and 2003, for individuals younger than 15 years who resided in the Curitiba metropolitan region.
  • The ratio of the adrenal NB and ACT age-adjusted mortality rates was 1.43.
  • [MeSH-major] Adrenal Cortex Neoplasms / mortality
  • [MeSH-minor] Adolescent. Brazil / epidemiology. Child. Child, Preschool. Genes, p53 / genetics. Humans. Incidence. Infant. Infant, Newborn. Mutation. Neuroblastoma / mortality. Survival Rate

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  • [Copyright] Copyright 2006 Wiley-Liss, Inc.
  • (PMID = 16200634.001).
  • [ISSN] 1545-5009
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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38. Merrot T, Oubejja H, Chaumoitre K, Alessandrini P: [Neonatal uro-haematoma secondary to posterior urethral valve]. Prog Urol; 2005 Feb;15(1):63-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The diagnosis of right perirenal extracapsular uro-haematoma secondary to posterior urethral valve was proposed on the basis of the antenatal clinical history.
  • The neonatal diagnosis of a heterogeneous renal cystic mass is sometimes difficult (polycystic renal dysplasia, cystic lymphangioma, cystic neuroblastoma, adrenal haematoma).
  • In some cases, the antenatal history may suggest the diagnosis of perirenal urohaematoma secondary to infravesical obstruction.

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  • (PMID = 15822395.001).
  • [ISSN] 1166-7087
  • [Journal-full-title] Progrès en urologie : journal de l'Association française d'urologie et de la Société française d'urologie
  • [ISO-abbreviation] Prog. Urol.
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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39. Gonçalves R, Linhares E, Albagli R, Valadão M, Vilhena B, Romano S, Ferreira CG: Occurrence of other tumors in patients with GIST. Surg Oncol; 2010 Dec;19(4):e140-3
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  • Immunohistological diagnosis was confirmed by a pathologist specialized in sarcomas.
  • The mean size of lesions was 4.79 cm (0.3-15 cm), with malignant potential low/very low in 7 cases (50%), intermediate in 5 cases (35.7%) and high in 2 cases (14.3%).
  • The diagnosis of GIST was incidental in 6 cases and in one case the non-GIST tumor was incidental.
  • The other sites involved were breast (ductal carcinoma), kidney (clear cell carcinoma), prostate (adenocarcinoma), endometrium (adenocarcinoma), ovary (adenocarcinoma) and adrenal (neuroblastoma), with one case each.

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  • [Copyright] Copyright © 2010 Elsevier Ltd. All rights reserved.
  • (PMID = 20675121.001).
  • [ISSN] 1879-3320
  • [Journal-full-title] Surgical oncology
  • [ISO-abbreviation] Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] Netherlands
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40. Roma J, Saus E, Cuadros M, Reventós J, Sánchez de Toledo J, Gallego S: Characterisation of novel splicing variants of the tyrosine hydroxylase C-terminal domain in human neuroblastic tumours. Biol Chem; 2007 Apr;388(4):419-26
MedlinePlus Health Information. consumer health - Neuroblastoma.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The mRNA distribution of these novel hTH isoforms in neuroblastic tumours and in foetal adrenal glands was analysed by conventional and real-time RT-PCR.
  • Their general distribution in neuroblastoma and adrenal glands and translation into protein suggest a significant functional role for these novel hTH isoforms, which merit further study.
  • [MeSH-major] Alternative Splicing / genetics. Neuroblastoma / enzymology. Tyrosine 3-Monooxygenase / genetics

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  • (PMID = 17391063.001).
  • [ISSN] 1431-6730
  • [Journal-full-title] Biological chemistry
  • [ISO-abbreviation] Biol. Chem.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Isoenzymes; 0 / Recombinant Proteins; EC 1.14.16.2 / Tyrosine 3-Monooxygenase
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41. Horiuchi A, Watanabe Y, Miyauchi K, Kawachi K, Ishida Y, Tokuda K, Tauchi H: Prenatally detected cystic adrenal neuroblastoma. Pediatr Int; 2008 Feb;50(1):130-1
MedlinePlus Health Information. consumer health - Neuroblastoma.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Prenatally detected cystic adrenal neuroblastoma.
  • [MeSH-major] Adrenal Gland Neoplasms / diagnosis. Neuroblastoma / diagnosis
  • [MeSH-minor] Cysts / pathology. Female. Humans. Infant, Newborn. Male. Pregnancy. Prenatal Diagnosis

  • Genetic Alliance. consumer health - Neuroblastoma.
  • MedlinePlus Health Information. consumer health - Adrenal Gland Cancer.
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  • (PMID = 18279224.001).
  • [ISSN] 1328-8067
  • [Journal-full-title] Pediatrics international : official journal of the Japan Pediatric Society
  • [ISO-abbreviation] Pediatr Int
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
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42. Tajiri S: [Vanillylmandelic acid (VMA) and homovanillic acid (HVA)]. Nihon Rinsho; 2005 Aug;63 Suppl 8:399-403

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-minor] Adrenal Gland Neoplasms / diagnosis. Biomarkers / analysis. Chromatography, High Pressure Liquid. Chronic Disease. Depressive Disorder / diagnosis. Hepatitis / diagnosis. Humans. Melanoma / diagnosis. Multiple System Atrophy / diagnosis. Neuroblastoma / diagnosis. Pheochromocytoma / diagnosis. Reference Values. Specimen Handling

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  • (PMID = 16149539.001).
  • [ISSN] 0047-1852
  • [Journal-full-title] Nihon rinsho. Japanese journal of clinical medicine
  • [ISO-abbreviation] Nippon Rinsho
  • [Language] jpn
  • [Publication-type] Journal Article; Review
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Biomarkers; 55-10-7 / Vanilmandelic Acid; X77S6GMS36 / Homovanillic Acid
  • [Number-of-references] 9
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