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Items 1 to 100 of about 4017
1. Watanabe M, Abe M, Ogawa S: A case of neonatal cardiac tamponade associated with benign hemangioma. J Nippon Med Sch; 2010 Feb;77(1):2-3
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  • [Title] A case of neonatal cardiac tamponade associated with benign hemangioma.
  • [MeSH-major] Cardiac Tamponade / etiology. Heart Neoplasms / complications. Hemangioma / complications
  • [MeSH-minor] Biopsy. Female. Humans. Infant, Newborn. Magnetic Resonance Imaging. Neoplasms / complications. Neoplasms / diagnosis. Neoplasms / surgery. Pregnancy. Ultrasonography, Prenatal

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  • (PMID = 20154451.001).
  • [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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2. Jia KD, Zou ZY, Lv DY: The Value of Survivin Gene and Proliferation of Hepatocytes in Screening for Hepatocellular Carcinoma. Gastroenterology Res; 2009 Dec;2(6):333-337
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  • BACKGROUND: The prospective surveillance programs on patients with liver diseases based on repeat ultrasound examinations of liver and serum α-fetoprotein (AFP) detection were reported having the probability of finding hepatocellular carcinoma (HCC) at its early stage, but it is time-consuming and not cost-effective.
  • Five liver specimens obtained from patients operated for hemangioma were used as normal control.

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  • (PMID = 27990202.001).
  • [ISSN] 1918-2805
  • [Journal-full-title] Gastroenterology research
  • [ISO-abbreviation] Gastroenterology Res
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Canada
  • [Keywords] NOTNLM ; Hepatocellular carcinoma / Liver cirrhosis / Proliferation / Proliferation cell nuclear antigen / Survivin gene
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3. Askri A, Mannai S, Landolsi S, Ben Farhat L, Said W, Dali N, Khalfallah MT, Hendaoui L: [Hepatic epithelioid hemangioendothelioma: review of 3 cases]. J Radiol; 2009 Mar;90(3 Pt 1):310-4
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  • [Transliterated title] Hémangioendothéliome épithélioïde hépatique: à propos de 3 cas.
  • EHE is an intermediate-grade malignancy, between benign hemangioma and angiosarcoma, with variable aggressiveness.
  • Involvement often is multinodular simulating metastases from a primatry extra-hepatic malignancy leading to delays in diagnosis.
  • [MeSH-major] Hemangioendothelioma, Epithelioid / diagnosis. Liver Neoplasms / diagnosis

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  • (PMID = 19421116.001).
  • [ISSN] 0221-0363
  • [Journal-full-title] Journal de radiologie
  • [ISO-abbreviation] J Radiol
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Contrast Media
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4. Ranalli NJ, Huang JH, Lee EB, Zhang PJ, Siegelman ES, Zager EL: Hemangiomas of the Brachial Plexus: A Case Series. Neurosurgery; 2009 Oct 01;65(suppl_4):A181-A188

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  • [Title] Hemangiomas of the Brachial Plexus: A Case Series.

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  • (PMID = 28180834.001).
  • [ISSN] 1524-4040
  • [Journal-full-title] Neurosurgery
  • [ISO-abbreviation] Neurosurgery
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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5. Kim MS, Pyo SY, Jeong YG, Lee SI, Jung YT, Sim JH: Gamma knife surgery for intracranial cavernous hemangioma. J Neurosurg; 2005 Jan;102(s_supplement):102-106

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  • [Title] Gamma knife surgery for intracranial cavernous hemangioma.
  • OBJECT: The purpose of this study was to assess the benefits of radiosurgery for cavernous hemangioma.
  • METHODS: Sixty-five cavernous hemangiomas were treated with gamma knife surgery (GKS) between October 1994 and December 2002.
  • CONCLUSIONS: The authors found that GKS was an effective treatment modality for cavernous hemangiomas, especially for those located within the brainstem, basal ganglia, or deep portions of the brain.

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  • (PMID = 28306472.001).
  • [ISSN] 1933-0693
  • [Journal-full-title] Journal of neurosurgery
  • [ISO-abbreviation] J. Neurosurg.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Keywords] NOTNLM ; cavernous hemangioma / gamma knife surgery / hemorrhage
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6. Nyáry I, Major O, Hanzély Z, Szeifert GT: Histopathological findings in a surgically resected thalamic cavernous hemangioma 1 year after 40-Gy irradiation. J Neurosurg; 2005 Jan;102(s_supplement):56-58

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  • [Title] Histopathological findings in a surgically resected thalamic cavernous hemangioma 1 year after 40-Gy irradiation.
  • ✓ Stereotactic radiosurgery is a controversial treatment modality in the management of cerebral cavernous hemangiomas (CHs), and results vary from center to center.

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  • (PMID = 28306459.001).
  • [ISSN] 1933-0693
  • [Journal-full-title] Journal of neurosurgery
  • [ISO-abbreviation] J. Neurosurg.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Keywords] NOTNLM ; cavernous hemangioma / histopathology / radiotherapy
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7. Altomare I, Desman G, Aledort LM: Echinocytosis--an unusual manifestation of hemangioma. Am J Hematol; 2006 Jul;81(7):532-4
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  • [Title] Echinocytosis--an unusual manifestation of hemangioma.
  • The case of a 21 year-old female with echinocytosis and a littoral cell hemangioma is reported.
  • A CT-recognized splenic mass led to splenectomy and a benign hemangioma was found.
  • This is the first case reported in the literature of echinocytosis as a consequence of a hemangioma.
  • [MeSH-major] Erythrocytes, Abnormal. Hemangioma / pathology. Spleen / pathology. Splenic Neoplasms / pathology

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  • (PMID = 16755560.001).
  • [ISSN] 0361-8609
  • [Journal-full-title] American journal of hematology
  • [ISO-abbreviation] Am. J. Hematol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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8. Cortés JJ, Bernabé JM, Riera N, Arenas JJ: [Intracranial cavernous angioma.]. Radiologia; 2009 Mar-Apr;51(2):190-3
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  • [Title] [Intracranial cavernous angioma.].
  • [Transliterated title] Angiomas cavernosos intracraneales.
  • We report the case of a 13-year-old boy who presented at the emergency department for nausea and vomiting with ataxia and dissymmetry.
  • Urgent CT and posterior MRI examination showed multiple supratentorial and infratentorial cavernous angiomas, one of which was located in the brainstem and presented acute hemorrhage, causing the symptoms.
  • The patient was initially managed conservatively, but the cavernous angioma in the brainstem was surgically extirpated after the patient's condition progressively worsened.
  • [MeSH-major] Brain Neoplasms. Hemangioma, Cavernous

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  • (PMID = 19286234.001).
  • [ISSN] 0033-8338
  • [Journal-full-title] Radiología
  • [ISO-abbreviation] Radiologia
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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9. Erkan AN, Bal N, Kiroglu E: A case report of hemangioendothelioma of the hard palate. B-ENT; 2008;4(3):175-8
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  • Hemangioendothelioma is a rare vascular tumour with potential for malignancy that is intermediate between that of a benign hemangioma and a malignant angiosarcoma.
  • In this report, we describe and discuss a case of hemangioendothelioma that originated in the hard palate of a 49-year-old woman.
  • [MeSH-major] Hemangioendothelioma / diagnosis. Hemangioendothelioma / surgery. Palatal Neoplasms / diagnosis. Palatal Neoplasms / surgery. Palate, Hard

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  • (PMID = 18949965.001).
  • [ISSN] 1781-782X
  • [Journal-full-title] B-ENT
  • [ISO-abbreviation] B-ENT
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Belgium
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10. Iba Y, Watanabe S, Akimoto T, Abe K, Koyanagi H: Pedicled cardiac hemangioma with right ventricular outflow tract obstruction. Jpn J Thorac Cardiovasc Surg; 2005 May;53(5):269-71
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  • [Title] Pedicled cardiac hemangioma with right ventricular outflow tract obstruction.
  • Histological examination revealed the nature of the tumor to be a benign hemangioma.
  • As reports of cardiac hemangioma causing severe RVOT obstruction are extremely rare, this case warrants attention.
  • [MeSH-major] Heart Neoplasms / complications. Hemangioma / complications. Ventricular Outflow Obstruction / etiology

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  • [Cites] Thorac Cardiovasc Surg. 1991 Aug;39(4):234-6 [1948975.001]
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  • (PMID = 15952321.001).
  • [ISSN] 1344-4964
  • [Journal-full-title] The Japanese journal of thoracic and cardiovascular surgery : official publication of the Japanese Association for Thoracic Surgery = Nihon Kyobu Geka Gakkai zasshi
  • [ISO-abbreviation] Jpn. J. Thorac. Cardiovasc. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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11. Scordi-Bello IA, Snyder A, Schwartz M, Fallon JT: Intravascular epithelioid hemangioendothelioma of the inferior vena cava: case report of an unusual and unpredictable vascular tumor. Cardiovasc Pathol; 2009 Jul-Aug;18(4):243-6
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  • Its biologic behavior lies somewhere between that of a benign hemangioma and that of a malignant angiosarcoma; however, it is unpredictable at best.

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  • (PMID = 18417368.001).
  • [ISSN] 1879-1336
  • [Journal-full-title] Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology
  • [ISO-abbreviation] Cardiovasc. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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12. Menon V, Saxena R, Chaudhary Z: Pontine cavernous hemangioma presenting with horizontal gaze palsy. Indian J Pediatr; 2005 Jan;72(1):86

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  • [Title] Pontine cavernous hemangioma presenting with horizontal gaze palsy.

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  • (PMID = 28378218.001).
  • [ISSN] 0973-7693
  • [Journal-full-title] Indian journal of pediatrics
  • [ISO-abbreviation] Indian J Pediatr
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
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13. Vourtsi A, Zervoudis S, Pafiti A, Athanasiadis S: Male breast hemangioma--a rare entity: a case report and review of the literature. Breast J; 2006 May-Jun;12(3):260-2
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  • [Title] Male breast hemangioma--a rare entity: a case report and review of the literature.
  • We report the case of a 77-year-old man with a very rare breast tumor: hemangioma.
  • The histology confirmed the diagnosis of benign hemangioma.
  • There has been no local recurrence after 9 years of follow-up.
  • Generally hemangiomas are large and ultrasound and magnetic resonance imaging (MRI) are useful for the diagnosis.
  • The important differential diagnosis with angiosarcoma is based on specific histologic patterns.
  • Moreover, malignant transformation of hemangioma is rare, but possible.
  • [MeSH-major] Breast Neoplasms, Male / diagnosis. Hemangioma / diagnosis

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  • (PMID = 16684325.001).
  • [ISSN] 1075-122X
  • [Journal-full-title] The breast journal
  • [ISO-abbreviation] Breast J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 15
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14. Kojima H, Yaguchi Y, Moriyama H: Middle ear hemangiona: a case report. Auris Nasus Larynx; 2008 Jun;35(2):255-9
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  • A middle ear hemangioma was detected in a 51-year-old man who suffered from fullness and hearing loss in the left ear.
  • The mass was surgically resected for diagnostic and therapeutic reasons, and pathologic examination revealed a benign hemangioma.
  • The significance of this diagnosis is also discussed.
  • [MeSH-major] Ear Neoplasms / diagnosis. Ear, Middle. Hemangioma / diagnosis

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  • (PMID = 17851004.001).
  • [ISSN] 0385-8146
  • [Journal-full-title] Auris, nasus, larynx
  • [ISO-abbreviation] Auris Nasus Larynx
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Netherlands
  • [Number-of-references] 16
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15. Sugiura M, Nakajima J, Morota T, Yamamoto T, Sano A, Fukami T, Murakawa T, Ota S, Takamoto S: [Posterior mediastinal hemangioma successfully resected with cardiopulmonary bypass; report of a case]. Kyobu Geka; 2007 Aug;60(9):857-60
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  • [Title] [Posterior mediastinal hemangioma successfully resected with cardiopulmonary bypass; report of a case].
  • Mediastinal hemangioma is a rare tumor.
  • We report a case of a 62-year-old woman with a posterior mediastinal hemangioma.
  • Histologically, the tumor was diagnosed as a benign hemangioma.
  • It was reported that hemangioma would reccur after subtotal excision.
  • [MeSH-major] Cardiopulmonary Bypass. Hemangioma / surgery. Mediastinal Neoplasms / surgery

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  • (PMID = 17703628.001).
  • [ISSN] 0021-5252
  • [Journal-full-title] Kyobu geka. The Japanese journal of thoracic surgery
  • [ISO-abbreviation] Kyobu Geka
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
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16. Ahlhelm F, Schulte-Altedorneburg G, Naumann N, Nabhan A, Reith W: [Imaging of extradural spinal lesions]. Radiologe; 2006 Dec;46(12):1035-43
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • In addition to real neoplasms, degenerative diseases, congenital abnormalities and inflammatory disorders can be causes of extradural masses.
  • Due to the bony boundary of the spinal canal, both benign as well as malignant masses can cause progressive neurological deficits including paraplegia.
  • Most of the spinal tumors are benign (hemangioma of the vertebral body, degenerative diseases).
  • In younger patients congenital abnormalities and primary tumors of the spine have to be considered, whereas in adults the list of differential diagnoses should include secondary malignancies such as metastases and lymphomas as well as metabolic disorders such as osteoporotic vertebral compression fracture and Paget's disease.
  • Cross-sectional imaging techniques such as magnetic resonance imaging (MRI) and computed tomography (CT) of the spine often help to make a specific diagnosis of extradural spinal lesions and represent important tools for tumor staging and preoperative evaluation.
  • [MeSH-major] Epidural Neoplasms / diagnosis. Magnetic Resonance Imaging. Spinal Diseases / diagnosis. Spinal Neoplasms / diagnosis. Tomography, Spiral Computed
  • [MeSH-minor] Diagnosis, Differential. Epidural Space / pathology. Humans. Neurologic Examination. Spinal Cord / pathology. Spinal Cord Compression / diagnosis. Spine / pathology

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  • (PMID = 17066265.001).
  • [ISSN] 0033-832X
  • [Journal-full-title] Der Radiologe
  • [ISO-abbreviation] Radiologe
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
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17. Papotti M, Arrondini M, Tavaglione V, Veltri A, Volante M: Diagnostic controversies in vascular proliferations of the thyroid gland. Endocr Pathol; 2008;19(3):175-83
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  • The differential diagnosis includes benign lesions on one side, i.e., endothelial reactive hyperplasia (Masson's "hemangioma") in goiter and hemangioma, and malignant tumors on the other, i.e., angiosarcomas and undifferentiated (angio)sarcomatoid carcinomas.
  • Benign reactive endothelial hyperplasia with atypias mimicking malignant tumors may occur in long-standing nodular goiter, as a result of spontaneous hemorrhage followed by granulation tissue and fibrous organization.
  • Angiosarcoma is a rare primary malignant thyroid tumor, mainly observed in endemic goiter areas displaying morphologic and phenotypical similar to those typical of angiosarcomas in other locations (including focal cytokeratin expression).
  • Other extremely rare vascular lesions or mimics in the thyroid include benign hemangioma and pseudo-angiosarcomatous variant of medullary carcinoma.
  • The differential diagnosis between benign and malignant vascular conditions in FNAB material is extremely challenging, and the cytopathology report should be remarkably cautious, especially in poorly cellular and highly hemorrhagic cases: atypias in endothelial cells are not per se indicative of malignancy, being a common feature of reactive endothelial hyperplasia in infracted goiter nodules as well.
  • [MeSH-major] Thyroid Diseases / pathology. Thyroid Gland / pathology. Vascular Diseases / pathology
  • [MeSH-minor] Diagnosis, Differential. Hemangioma / pathology. Hemangiosarcoma / pathology. Humans. Hyperplasia / pathology

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  • (PMID = 18766472.001).
  • [ISSN] 1046-3976
  • [Journal-full-title] Endocrine pathology
  • [ISO-abbreviation] Endocr. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] United States
  • [Number-of-references] 38
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18. Mehrabi A, Kashfi A, Schemmer P, Sauer P, Encke J, Fonouni H, Friess H, Weitz J, Schmidt J, Büchler MW, Kraus TW: Surgical treatment of primary hepatic epithelioid hemangioendothelioma. Transplantation; 2005 Sep 27;80(1 Suppl):S109-12
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  • It can range from benign hemangioma to malignant hemangioendotheliosarcoma.
  • Until now, no recurrence of local tumor or distant metastases could be observed during follow-up in our series.

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  • (PMID = 16286886.001).
  • [ISSN] 0041-1337
  • [Journal-full-title] Transplantation
  • [ISO-abbreviation] Transplantation
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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19. Giannitrapani L, Soresi M, La Spada E, Cervello M, D'Alessandro N, Montalto G: Sex hormones and risk of liver tumor. Ann N Y Acad Sci; 2006 Nov;1089:228-36
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  • Long-term use of oral contraceptives (OCs) and anabolic androgenic steroids (AASs) can induce both benign (hemangioma, adenoma, and focal nodular hyperplasia [FNH]) and malignant (hepatocellular carcinoma [HCC]) hepatocellular tumors.
  • Hepatic adenomas (HAs) are rare, benign neoplasms usually occurring in young women, the development and the complications of which have been related to the strength of OCs and the duration of their use.
  • FNH is a benign lesion, most commonly seen in young women, which is thought to represent a local hyperplastic response of hepatocytes to a vascular abnormality.
  • Liver hemangiomas (LHs) are the most common benign liver tumors and are seen more commonly in young adult females.
  • However, regardless of etiology, chronic liver diseases progress at unequal rates in the two sexes, with the major sequelae, such as cirrhosis and HCC, being more frequent in men than in women.

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  • (PMID = 17261770.001).
  • [ISSN] 0077-8923
  • [Journal-full-title] Annals of the New York Academy of Sciences
  • [ISO-abbreviation] Ann. N. Y. Acad. Sci.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Gonadal Steroid Hormones; 0 / Receptors, Androgen; 0 / Receptors, Estrogen
  • [Number-of-references] 38
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20. Liscák R, Vladyka V, Simonová G, Vymazal J, Novotny J Jr: Gamma knife surgery of brain cavernous hemangiomas. J Neurosurg; 2005 Jan;102(s_supplement):207-213

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Gamma knife surgery of brain cavernous hemangiomas.
  • OBJECT: The authors conducted a study to record more detailed information about the natural course and factors predictive of outcome following gamma knife surgery (GKS) for cavernous hemangiomas.
  • METHODS: One hundred twelve patients with brain cavernous hemangiomas underwent GKS between 1993 and 2000.
  • One hundred seven patients were followed for a median of 48 months (range 6-114 months).
  • Two patients with brainstem cavernous hemangiomas died due to rebleeding.
  • CONCLUSIONS: Gamma knife surgery of cavernous hemangiomas can produce an acceptable rate of morbidity, which can be reduced by using a lower margin dose.

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  • (PMID = 28306451.001).
  • [ISSN] 1933-0693
  • [Journal-full-title] Journal of neurosurgery
  • [ISO-abbreviation] J. Neurosurg.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Keywords] NOTNLM ; cavernous hemangioma / gamma knife surgery / hemorrhage
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21. Novitzky D, Guglin M, Sheffield C: Cardiac autotransplantation for removal of left atrial hemangioma and a review of the literature. Heart Surg Forum; 2009 Oct;12(5):E279-84
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  • [Title] Cardiac autotransplantation for removal of left atrial hemangioma and a review of the literature.
  • We describe the management of a patient who presented with symptoms of severe congestive heart failure.
  • The pathology diagnosis was a benign cavernous hemangioma.
  • Placement of a pacemaker was not required because the patient retained the sinus rhythm.
  • To our knowledge, this report is the first of cardiac autotransplantation for benign hemangioma.
  • [MeSH-major] Heart Atria / surgery. Heart Failure / surgery. Heart Neoplasms / surgery. Hemangioma, Cavernous / surgery. Replantation / methods

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  • (PMID = 19833595.001).
  • [ISSN] 1522-6662
  • [Journal-full-title] The heart surgery forum
  • [ISO-abbreviation] Heart Surg Forum
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 38
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22. Liu KD, Chung WY, Wu HM, Shiau CY, Wang LW, Guo WY, Hung-Chi Pan D: Gamma knife surgery for cavernous hemangiomas: an analysis of 125 patients. J Neurosurg; 2005 Jan;102(s_supplement):81-86

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  • [Title] Gamma knife surgery for cavernous hemangiomas: an analysis of 125 patients.
  • OBJECT: The authors sought to determine the value of gamma knife surgery (GKS) in the treatment of cavernous hemangiomas (CHs).

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  • (PMID = 28306449.001).
  • [ISSN] 1933-0693
  • [Journal-full-title] Journal of neurosurgery
  • [ISO-abbreviation] J. Neurosurg.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Keywords] NOTNLM ; cavernous hemangioma / complication / gamma knife surgery / hemorrhage / seizure
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23. Poenitz N, Koenen W, Utikal J, Goerdt S: [Angioma serpiginosum following the lines of Blaschko--an effective treatment with the IPL technology]. J Dtsch Dermatol Ges; 2006 Aug;4(8):650-3
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  • [Title] [Angioma serpiginosum following the lines of Blaschko--an effective treatment with the IPL technology].
  • [Transliterated title] Angioma serpiginosum in den Blaschkolinien--eine effektive Behandlung mit der IPL Technik.
  • Angioma serpiginosum, first described by Hutchinson in 1889, is a rare benign vascular nevus with dilatation and proliferation of the capillaries in the upper dermis.
  • A 15-year-old boy presented with an angioma serpiginosum on the right side of the body following the lines of Blaschko.
  • [MeSH-major] Hemangioma / pathology. Hemangioma / therapy. Phototherapy / methods. Skin Neoplasms / pathology. Skin Neoplasms / therapy

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  • (PMID = 16895567.001).
  • [ISSN] 1610-0379
  • [Journal-full-title] Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
  • [ISO-abbreviation] J Dtsch Dermatol Ges
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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24. Bienaimé A, Rojat-Habib MC, Hesse S, Pelissier JF, Bonerandi JJ: [Giant vascular tumour in an adult: tufted angioma or kaposiform hemangioendothelioma]. Ann Dermatol Venereol; 2006 Jun-Jul;133(6-7):553-6
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  • [Title] [Giant vascular tumour in an adult: tufted angioma or kaposiform hemangioendothelioma].
  • [Transliterated title] Tumeur vasculaire géante de l'adulte: angiome en touffe ou hémangioendothéliome kaposiforme.
  • INTRODUCTION: Tufted angioma and kaposiform hemangioendothelioma are two rare benign but aggressive vascular tumours that occur mainly in children.
  • OBSERVATION: A 72 year-old man consulted for a 50 cm wide vascular tumour of the right shoulder which was increasing for 10 years.
  • On histological examination there were features of tufted angioma and kaposiform hemangioendothelioma.
  • The histological association of aspects which could correspond to tufted angioma and kaposiform hemangioendothelioma seems to confirm recent publications which support the hypothesis that these two tumours are two evolutive stages of one and only entity.
  • [MeSH-major] Hemangioendothelioma / pathology. Hemangioma / pathology. Skin Neoplasms / pathology


25. Chanfi M: [Tuberous angioma in an infant: a case study]. J Fr Ophtalmol; 2005 Sep;28(7):774
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  • [Title] [Tuberous angioma in an infant: a case study].
  • [Transliterated title] Angiome immature chez un nourrisson. A propos d'un cas.
  • Tuberous angioma of the orbit is the most frequent benign tumor of the orbit in children.
  • Angiomatous tumors in general, and more particularly tuberous angioma tumors, are classed among the primary tumors of the orbit.
  • The author reports the clinical observation of a giant tuberous angioma the entire left lower eyelid radiating throughout the left cheek of a 2-month-old infant.
  • [MeSH-major] Eyelid Neoplasms. Hemangioma

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  • (PMID = 16208215.001).
  • [ISSN] 1773-0597
  • [Journal-full-title] Journal français d'ophtalmologie
  • [ISO-abbreviation] J Fr Ophtalmol
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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26. Revert Ventura AJ, Martí-Bonmatí L, Poyatos Ruipérez C, Pallardó Calatayud Y, Arana E, Mollá Olmos E: [Association of cavernous and venous angiomas]. Neurologia; 2007 Dec;22(10):839-45
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  • [Title] [Association of cavernous and venous angiomas].
  • [Transliterated title] Asociación de angiomas cavernosos con venosos.
  • INTRODUCTION: Isolated cavernous and venous angiomas are common vascular cerebral malformations.
  • OBJECTIVE: An analysis of the association characteristics of both lesions (cavernous and venous angiomas), and the relationships with localization, size, patient sex and the use of intravenous contrast material in the diagnosis with MR.
  • METHODS: A retrospective analysis of the cerebral MRI studies of 37 patients with cavernous angiomas.
  • Results. 52 cavernous angiomas were identified in the 37 patients.
  • No significant statistical differences were found that related the cavernous angioma size, localization or patient sex with the existence of an associated venous angioma.
  • Only the administration of contrast material has shown a statistical significance for the diagnosis.
  • CONCLUSIONS: The association of cavernous and venous angioma is frequent (30%).
  • To detect venous angiomas is necessary the administration of contrast material.
  • [MeSH-major] Brain / blood supply. Brain Neoplasms / diagnosis. Hemangioma / diagnosis. Hemangioma, Cavernous / diagnosis. Magnetic Resonance Imaging

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  • (PMID = 17671855.001).
  • [ISSN] 0213-4853
  • [Journal-full-title] Neurología (Barcelona, Spain)
  • [ISO-abbreviation] Neurologia
  • [Language] spa
  • [Publication-type] Editorial; English Abstract
  • [Publication-country] Spain
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27. González-Darder JM, Pesudo-Martínez JV, Merino-Peña J: [Trigonal cavernous angioma: case report]. Neurocirugia (Astur); 2007 Aug;18(4):330-2
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  • [Title] [Trigonal cavernous angioma: case report].
  • [Transliterated title] Angioma cavernoso del trígono ventricular. Caso clínico.
  • The authors report on an intraventricular cavernous angioma located at the right trigone in a 25-year-old male patient presented with a predominantly intralesional haemorrhage.
  • Neuroimaging led to an accurate preoperative diagnosis although the typical low intensity perilesional ring of gliosis and hemosiderin was not present.
  • [MeSH-major] Cerebral Ventricle Neoplasms / pathology. Hemangioma, Cavernous / pathology

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  • (PMID = 17882341.001).
  • [ISSN] 1130-1473
  • [Journal-full-title] Neurocirugía (Asturias, Spain)
  • [ISO-abbreviation] Neurocirugia (Astur)
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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28. Kreusel KM, Bechrakis NE, Neumann HP, Foerster MH: [Juxtapapillary capillary retinal angioma with epiretinal membrane of the macula in familial Von-Hippel-Lindau-Syndrome]. Ophthalmologe; 2007 Apr;104(4):317-20
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  • [Title] [Juxtapapillary capillary retinal angioma with epiretinal membrane of the macula in familial Von-Hippel-Lindau-Syndrome].
  • [Transliterated title] Juxtapapilläres kapilläres retinales Angiom mit epiretinaler Membran der Makula bei familiärem Von-Hippel-Lindau-Syndrom.
  • A case of juxtapapillary capillary retinal angioma associated with a vascularized epiretinal membrane of the macula in a 6-year-old girl is presented.
  • The retinal angioma embedded in an epiretinal membrane was removed completely with the membrane by pars plana vitrectomy with a good functional result.
  • Histopathology confirmed the diagnosis of capillary angioma.
  • [MeSH-major] Epiretinal Membrane / surgery. Hemangioma, Capillary / genetics. Hemangioma, Capillary / surgery. Retinal Neoplasms / genetics. Retinal Neoplasms / surgery. von Hippel-Lindau Disease / genetics. von Hippel-Lindau Disease / surgery

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  • (PMID = 17123050.001).
  • [ISSN] 0941-293X
  • [Journal-full-title] Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft
  • [ISO-abbreviation] Ophthalmologe
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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29. Altmann S, Fansa H, Schildhaus HU, Schneider W: [Intramuscular angioma in the hand. A case report]. Orthopade; 2005 Apr;34(4):352-5
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  • [Title] [Intramuscular angioma in the hand. A case report].
  • [Transliterated title] Intramuskuläre Angiome der Hand. Ein Fallbericht.
  • Intramuscular angiomas are rare vascular tumors with locally aggressive growth between the fibers of muscle.
  • We report the case of a 32-year-old woman with a painless tumor in the thenar.
  • Physical examination showed a 2 x 3 x 5 cm fixed and engorged swelling.
  • Histologic examination after local resection showed an intramuscular angioma.
  • Intramuscular angiomas have a malignant aspect because of the rapid and infiltrative growth followed by functional impairment, pain, and deformity.
  • [MeSH-major] Hemangioma / diagnosis. Muscle Neoplasms / diagnosis. Thumb / pathology. Thumb / radiography

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  • (PMID = 15726321.001).
  • [ISSN] 0085-4530
  • [Journal-full-title] Der Orthopäde
  • [ISO-abbreviation] Orthopade
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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30. Marcos Toledano MM, Portilla Cuenca JC, Porras Estrada LF, Gómez Perals L: [Pseudo-emesis gravidarum caused by complicated cerebral venous angioma]. Neurologia; 2006 Mar;21(2):92-5
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  • [Title] [Pseudo-emesis gravidarum caused by complicated cerebral venous angioma].
  • [Transliterated title] Seudoemesis gravídica causada por angioma venoso cerebral complicado.
  • On the other hand, venous angioma (VA) is the most frequent cerebral vascular malformation.
  • In fact, it is a variant of the normal venous drainage of the brain and it is usually an incidental finding.
  • VA is rarely symptomatic, unless associated with cavernous angiomas.
  • Neuroradiological studies showed a choroid plexus haematoma from left lateral ventricle to third ventricle, secondary to the existence of a left parietal VA, without demonstration of associated cavernous angioma.
  • CONCLUSIONS: Although it is rare, a supratentorial VA, without associated cavernous angioma, may lead to intraventricular hemorrhage.
  • [MeSH-major] Central Nervous System Venous Angioma / pathology. Vomiting

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  • (PMID = 16525915.001).
  • [ISSN] 0213-4853
  • [Journal-full-title] Neurología (Barcelona, Spain)
  • [ISO-abbreviation] Neurologia
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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31. Pino Rivero V, González Palomino A, Pantoja Hernández CG, Trinidad Ruíz G, Marqués Rebollo L, Blasco Huelva A: [Pontine cavernous angioma (cavernoma) with initial ENT manifestations]. An Otorrinolaringol Ibero Am; 2006;33(1):35-40
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  • [Title] [Pontine cavernous angioma (cavernoma) with initial ENT manifestations].
  • [Transliterated title] Angioma cavernoso del tronco cerebral (cavernoma) con manifestaciones orl iniciales.
  • We report the case of a 22 years old female who consulted us for facial parestesias, hearing loss in right ear and sudden tinnitus.
  • Her audiometry showed an unilateral discreet sensorineural hipoacusia and the cranial IRM, a mass of 20 mm diameter in right pontine region and bulbus informed as cavernous angioma with signs of recent bleeding.
  • [MeSH-major] Central Nervous System Neoplasms / complications. Central Nervous System Neoplasms / pathology. Hearing Loss / diagnosis. Hearing Loss / etiology. Hemangioma, Cavernous, Central Nervous System / complications. Hemangioma, Cavernous, Central Nervous System / pathology. Pons / pathology
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Humans. Magnetic Resonance Imaging

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  • (PMID = 16566194.001).
  • [ISSN] 0303-8874
  • [Journal-full-title] Anales otorrinolaringológicos ibero-americanos
  • [ISO-abbreviation] An Otorrinolaringol Ibero Am
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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32. Repiso A, Gómez Rodríguez R, González de Frutos C, de Artaza T, Sánchez Ruano JJ, Pérez Grueso MJ, Martínez Potenciano JL: [Angioma-like liver lesions in patients with chronic liver disease]. Rev Esp Enferm Dig; 2007 May;99(5):259-63
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Angioma-like liver lesions in patients with chronic liver disease].
  • [Transliterated title] Lesiones hepáticas sugestivas de angioma en pacientes con hepatopatía crónica.
  • OBJECTIVE: The aim of this study was to evaluate in our healthcare area the clinical, ultrasonographic, and evolutionary features of patients with chronic liver disease and angioma-like liver lesions on ultrasonography.
  • Included in the study were patients that presented with clinical and/or laboratory complaints consistent with chronic liver disease of any etiology, and those in which abdominal ultrasounds revealed the existence of at least one angioma-like liver lesion.
  • RESULTS: In the course of our study, 58 patients were diagnosed with chronic liver disease and angioma-like liver lesions, of which 13 showed clinical, laboratory, ultrasonographic, and/or histological signs of liver cirrhosis.
  • During an average follow-up period of 35 months (6-168 months) we verified that, in two patients, these lesions, initially interpreted as angiomas were in fact malignancies (one hepatocellular carcinoma and one metastatic adenocarcinoma of the gallbladder).
  • Thus, our study revealed that 15% of lesions found in cirrhotic patients initially interpreted as angiomas were actually malignant.
  • CONCLUSIONS: Our study revealed that, in patients with chronic liver disease, particularly in cirrhotic patients, a considerable percentage of ultrasonographic lesions originally interpreted as angiomas are in fact malignant tumors.
  • [MeSH-major] Hemangioma / ultrasonography. Liver Cirrhosis / ultrasonography. Liver Neoplasms / ultrasonography
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Chronic Disease. Female. Humans. Liver Diseases / ultrasonography. Male. Middle Aged. Retrospective Studies

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  • (PMID = 17650934.001).
  • [ISSN] 1130-0108
  • [Journal-full-title] Revista española de enfermedades digestivas : organo oficial de la Sociedad Española de Patología Digestiva
  • [ISO-abbreviation] Rev Esp Enferm Dig
  • [Language] spa
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Spain
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33. Browning J, Frieden I, Baselga E, Wagner A, Metry D: Congenital, self-regressing tufted angioma. Arch Dermatol; 2006 Jun;142(6):749-51
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Congenital, self-regressing tufted angioma.
  • BACKGROUND: Tufted angioma (known in Japanese literature as angioblastoma of Nakagawa) is an uncommon, histologically benign, vascular tumor.
  • OBSERVATIONS: We present a series of 5 histopathologically confirmed cases of congenital tufted angioma that spontaneously regressed during infancy or early childhood.
  • CONCLUSION: We recommend that observation for potential regression be considered for otherwise uncomplicated congenital or early infantile cases of tufted angioma.
  • [MeSH-major] Hemangioma, Capillary / diagnosis. Neoplasm Regression, Spontaneous / pathology. Skin Neoplasms / diagnosis
  • [MeSH-minor] Arm. Cheek. Diagnosis, Differential. Female. Forearm. Forehead. Humans. Infant. Infant, Newborn. Male. Shoulder

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  • (PMID = 16785378.001).
  • [ISSN] 0003-987X
  • [Journal-full-title] Archives of dermatology
  • [ISO-abbreviation] Arch Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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34. Gómez-Díez S, Losada A, Coto P, Soler T, Pérez-Oliva N: [Acquired flat angiomas in the form of a port-wine stain]. Actas Dermosifiliogr; 2006 Jan-Feb;97(1):62-4
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  • [Title] [Acquired flat angiomas in the form of a port-wine stain].
  • [Transliterated title] Angiomas planos adquiridos en mancha de vino de Oporto.
  • The development of flat angiomas in the form of a "port-wine stain" is an infrequent event in adults.
  • We describe two cases of acquired flat angioma in the form of a "port-wine stain", which began in the second decade of life and grew slowly and steadily until reaching a large size.
  • [MeSH-major] Hemangioma / pathology. Port-Wine Stain / pathology. Skin Neoplasms / pathology

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  • (PMID = 16540056.001).
  • [ISSN] 0001-7310
  • [Journal-full-title] Actas dermo-sifiliográficas
  • [ISO-abbreviation] Actas Dermosifiliogr
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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35. Santos-Ditto RA, Santos-Franco JA, Pinos-Gavilanes MW: [Cavernous angioma of the second cranial nerve and chiasmatic apoplexy]. Neurocirugia (Astur); 2007 Feb;18(1):47-51
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  • [Title] [Cavernous angioma of the second cranial nerve and chiasmatic apoplexy].
  • [Transliterated title] Angioma cavernoso del segundo nervio craneal y apoplejía quiasmática.
  • We present the case of a female patient who developed chiasmatic apoplexy and menstrual alterations.
  • She underwent surgery with the presumptive diagnosis of pituitary tumor.
  • Cavernous angioma was diagnosed by histopathology.
  • Cavernous angiomas constitute nearly 15% of all central nervous system vascular malformations.
  • Location at the optic pathway is very rare, but must to be ruled out in the diagnosis of a patient with chiasmatic and/or optic apoplexy.
  • [MeSH-major] Hemangioma, Cavernous / complications. Optic Chiasm / blood supply. Optic Nerve Neoplasms / complications. Stroke / etiology
  • [MeSH-minor] Adenoma / diagnosis. Adult. Craniotomy. Diagnosis, Differential. Emergencies. Female. Headache / etiology. Humans. Microsurgery. Pituitary Apoplexy / diagnosis. Pituitary Neoplasms / diagnosis. Tomography, X-Ray Computed. Vision Disorders / etiology. Visual Fields

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  • (PMID = 17393047.001).
  • [ISSN] 1130-1473
  • [Journal-full-title] Neurocirugía (Asturias, Spain)
  • [ISO-abbreviation] Neurocirugia (Astur)
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Spain
  • [Number-of-references] 35
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36. González-Darder JM, Pesudo-Martinéz JV: [Facial nerve palsy due to cavernous angioma of the petrous bone. Case report]. Neurocirugia (Astur); 2007 Feb;18(1):44-6
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  • [Title] [Facial nerve palsy due to cavernous angioma of the petrous bone. Case report].
  • [Transliterated title] Parálisis facial por angioma cavernoso del peñasco. Caso clínico.
  • We present the case of a patient with a temporal bone cavernoma and symptoms of a torpid peripheral facial House-Brackmann grade IV nerve palsy with dry eye and loss of stapedial reflex.
  • The routine computed tomographic and magnetic resonance imaging studies showed no abnormalities, but the same imaging techniques done after the clinical suspiction identified a less that 1cm lesion that was compatible with an osseous cavernous angioma.
  • [MeSH-major] Bone Neoplasms / complications. Facial Nerve / physiopathology. Facial Paralysis / etiology. Hemangioma, Cavernous / complications. Nerve Compression Syndromes / etiology. Petrous Bone / blood supply

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  • (PMID = 17393046.001).
  • [ISSN] 1130-1473
  • [Journal-full-title] Neurocirugía (Asturias, Spain)
  • [ISO-abbreviation] Neurocirugia (Astur)
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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37. Mac New HG, Fowler CL: Partial splenectomy for littoral cell angioma. J Pediatr Surg; 2008 Dec;43(12):2288-90
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  • [Title] Partial splenectomy for littoral cell angioma.
  • Littoral cell angioma is a rare primary splenic tumor that is difficult to differentiate preoperatively from other benign and malignant splenic lesions and may have immunogenic origins.
  • Total splenectomy is usually required because littoral cell angioma is generally large and/or diffuse.
  • However, a partial splenectomy was able to be performed, making this the first reported partial splenectomy for littoral cell angioma.
  • [MeSH-major] Hemangioma / surgery. Splenectomy / methods. Splenic Neoplasms / surgery
  • [MeSH-minor] Abdominal Injuries / complications. Accidents, Traffic. Adolescent. Anemia / complications. Diagnosis, Differential. Diagnostic Errors. Female. Hematoma / diagnosis. Humans. Hypersensitivity / complications. Hypertension / complications. Immunocompromised Host. Incidental Findings. Lupus Erythematosus, Systemic / complications. Lymphoma, Non-Hodgkin / diagnosis. Polypharmacy. Tomography, X-Ray Computed

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  • (PMID = 19040956.001).
  • [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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38. Schaffer JV, Fangman W, Bossenbroek NM, Meehan SA, Kamino H: Tufted angioma. Dermatol Online J; 2008;14(10):20
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Tufted angioma.
  • Histopathologic evaluation showed multiple, discrete lobules of tightly packed capillaries in a 'cannonball' pattern within the dermis, which confirmed the diagnosis of tufted angioma.
  • The clinical and histopathologic features, natural history, and treatment options for tufted angiomas are reviewed; their relationship to kaposiform hemangioendotheliomas is discussed.
  • [MeSH-major] Hemangioma / diagnosis. Skin Neoplasms / diagnosis


39. Melone AG, Delfinis CP, Passacantilli E, Lenzi J, Santoro A: Intracranial extra-axial cavernous angioma of the cerebellar falx. World Neurosurg; 2010 Oct-Nov;74(4-5):501-4
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  • [Title] Intracranial extra-axial cavernous angioma of the cerebellar falx.
  • INTRODUCTION: Intracranial cavernous hemangiomas are benign vascular malformations that can be divided into intra-axial and extra-axial types.
  • Extra-axial cavernous angiomas (or hemangiomas) are rare lesions; intracranially, they arise in relation to the dura mater or at a spinal level mimicking meningiomas.
  • CASE REPORT: The authors report a case of a cavernous angioma that occurred in the cerebellar falx of a 58-year-old man.
  • The patient underwent surgery with en-bloc removal of the tumor.
  • CONCLUSION: Intra-axial and extra-axial cavernous angiomas are histopathologically identical lesions, but by the radiological features, it is very difficult to distinguish the extra-axial cavernous angiomas from meningiomas, especially when dural tail sign and calcification are present.
  • [MeSH-major] Cerebellar Neoplasms / pathology. Dura Mater / pathology. Hemangioma, Cavernous, Central Nervous System / pathology. Infratentorial Neoplasms / pathology. Meningeal Neoplasms / pathology

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  • [Copyright] Copyright © 2010 Elsevier Inc. All rights reserved.
  • (PMID = 21492602.001).
  • [ISSN] 1878-8769
  • [Journal-full-title] World neurosurgery
  • [ISO-abbreviation] World Neurosurg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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40. Kim JS, Yang SH, Kim MK, Hong YK: Cavernous angioma in the falx cerebri: a case report. J Korean Med Sci; 2006 Oct;21(5):950-3
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  • [Title] Cavernous angioma in the falx cerebri: a case report.
  • Intracranial cavernous angiomas are benign vascular malformations and can be divided into intra-axial and extra-axial lesions.
  • Extra-axial cavernous angiomas are relatively rare and usually arise in relation to the dura mater and mimick meningiomas.
  • We report a case of cavernous angioma that occurred in the falx cerebri of a 22-yr-old female patient with the special focus on neuroradiologic findings.
  • This is the fourth case of cavernous angioma in the falx cerebri reported in the literature to our knowledge.
  • [MeSH-major] Dura Mater / pathology. Hemangioma, Cavernous / radiography. Meningeal Neoplasms / radiography

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  • (PMID = 17043437.001).
  • [ISSN] 1011-8934
  • [Journal-full-title] Journal of Korean medical science
  • [ISO-abbreviation] J. Korean Med. Sci.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2722013
  •  go-up   go-down


41. Priego P, Rodríguez Velasco G, Griffith PS, Fresneda V: Littoral cell angioma of the spleen. Clin Transl Oncol; 2008 Jan;10(1):61-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Littoral cell angioma of the spleen.
  • Littoral cell angiomas (LCAs) are rare splenic vascular neoplasms that arise from the cells lining the red pulp sinuses.
  • The clinical course is benign and in most cases asymptomatic.
  • The definitive diagnosis is made on histology and confirmed with immunohistochemistry.
  • The use of percutaneous fine-needle aspiration biopsy (FNA) in preoperative diagnosis is controversial.
  • [MeSH-major] Hemangioma / pathology. Splenic Neoplasms / pathology

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  • [Cites] AJR Am J Roentgenol. 2002 Dec;179(6):1591-6 [12438060.001]
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  • (PMID = 18208795.001).
  • [ISSN] 1699-048X
  • [Journal-full-title] Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
  • [ISO-abbreviation] Clin Transl Oncol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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42. Corapçioğlu F, Akansel G, Gönüllü E, Yildiz K, Etuş V: Fatal giant pediatric intracranial cavernous angioma. Turk J Pediatr; 2006 Jan-Mar;48(1):89-92
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  • [Title] Fatal giant pediatric intracranial cavernous angioma.
  • Cavernous angioma is a benign vascular lesion that may occur in the central nervous system.
  • A diagnosis of brain death was made.
  • A cavernous hemangioma was diagnosed with pathologic examination.
  • In conclusion, a cavernous angioma may occasionally follow a rapid and fatal course by causing gross hemorrhage in the pediatric age group.
  • [MeSH-major] Brain Neoplasms / diagnosis. Hemangioma, Cavernous / diagnosis

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  • (PMID = 16562795.001).
  • [ISSN] 0041-4301
  • [Journal-full-title] The Turkish journal of pediatrics
  • [ISO-abbreviation] Turk. J. Pediatr.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Turkey
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43. Namazi MR, Maghsoodi M: Association of angiokeratoma of the vulva with angioma serpiginosum. J Drugs Dermatol; 2008 Sep;7(9):882-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Association of angiokeratoma of the vulva with angioma serpiginosum.
  • Angioma serpiginosum is a rare benign vascular disorder usually beginning in childhood.
  • [MeSH-major] Angiokeratoma / pathology. Hemangioma / pathology. Vulvar Neoplasms / pathology

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  • (PMID = 19112804.001).
  • [ISSN] 1545-9616
  • [Journal-full-title] Journal of drugs in dermatology : JDD
  • [ISO-abbreviation] J Drugs Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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44. Toldo I, Drigo P, Mammi I, Marini V, Carollo C: Vertebral and spinal cavernous angiomas associated with familial cerebral cavernous malformation. Surg Neurol; 2009 Feb;71(2):167-71
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  • [Title] Vertebral and spinal cavernous angiomas associated with familial cerebral cavernous malformation.
  • Until now, vertebral hemangiomas associated with CCM have been described only in one case.
  • The coexistence of intracranial and spinal cavernous angiomas in familial CCM is extremely rare.
  • In addition to previous studies, the occurrence of spinal, vertebral, and cutaneous cavernous angiomas is now described in different members of a large family with CCM.
  • CASE DESCRIPTION: Our study reports a previously described family (IFCAS-07) with 12 members affected by autosomal dominant cavernous angiomas: 11 had CCM either alone or associated with hepatic or retinal angiomas, and one had only hepatic angioma.
  • Spinal MRI showed in 5 subjects spinal cavernous angiomas either alone or associated with vertebral hemangiomas.
  • CONCLUSIONS: To our knowledge, this is the largest family reported with different subjects affected by CCM associated with multiple cavernous angiomas throughout (brain and spinal cord) and besides (retina, skin, liver, and vertebral column) the CNS.
  • We emphasize the importance of spinal MRI in the diagnosis of spinal and vertebral cavernous angiomas in all patients affected by familial CCM.
  • [MeSH-major] Central Nervous System Neoplasms / etiology. Central Nervous System Vascular Malformations / complications. Hemangioma, Cavernous / etiology. Spinal Neoplasms / etiology
  • [MeSH-minor] Adult. Cohort Studies. Female. Humans. Male. Microtubule-Associated Proteins / genetics. Middle Aged. Pedigree. Proto-Oncogene Proteins / genetics. Skin Neoplasms / diagnosis. Skin Neoplasms / etiology. Skin Neoplasms / therapy. Young Adult

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  • (PMID = 18207546.001).
  • [ISSN] 0090-3019
  • [Journal-full-title] Surgical neurology
  • [ISO-abbreviation] Surg Neurol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / KRIT1 protein, human; 0 / Microtubule-Associated Proteins; 0 / Proto-Oncogene Proteins
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45. Wang YJ, Li F, Cao F, Sun JB, Liu JF, Wang YH: Littoral cell angioma of the spleen. Asian J Surg; 2009 Jul;32(3):167-71
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Littoral cell angioma of the spleen.
  • Littoral cell angioma (LCA) is a rare primary benign vascular neoplasm of the spleen.
  • The case of a 52-year-old female with LCA is reported.
  • This is the first report of a LCA combined with gallbladder stones.

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  • (PMID = 19656757.001).
  • [ISSN] 0219-3108
  • [Journal-full-title] Asian journal of surgery
  • [ISO-abbreviation] Asian J Surg
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] China
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46. Tee M, Vos P, Zetler P, Wiseman SM: Incidental littoral cell angioma of the spleen. World J Surg Oncol; 2008;6:87
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Incidental littoral cell angioma of the spleen.
  • BACKGROUND: Littoral cell angioma (LCA) is a recently described primary vascular neoplasm of the spleen that may be associated with other malignancies and may itself also have malignant potential.
  • Post-operative outcome was favourable with no evidence of complication or recurrent disease.
  • CONCLUSION: LCA is a rare, generally benign, primary vascular tumour of the spleen that typically is discovered incidentally.
  • [MeSH-major] Hemangioma / diagnosis. Splenic Neoplasms / diagnosis
  • [MeSH-minor] Cholecystectomy. Colic / surgery. Diagnosis, Differential. Female. Humans. Magnetic Resonance Imaging. Middle Aged. Tomography, X-Ray Computed

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  • (PMID = 18713469.001).
  • [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/ PMC2527567
  •  go-up   go-down


47. Varoglu AO, Tan H, Onbas O, Tuzun Y, Deniz O, Gursan N: Intramedullary angioma with bilateral arm hypothermia. Br J Neurosurg; 2008 Oct;22(5):687-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Intramedullary angioma with bilateral arm hypothermia.
  • They are rare and frequently accompany cranial cavernous angiomas.
  • We present a 12-year-old boy with bilateral hypothermia predominantly in the left arm and motor weakness of the upper extremities, and lesser involvement of the lower extremities The case had normal cranial magnetic resonance imaging, but MRI of cervical region revealed an intramedullary cavernous haemangioma confirmed with histopathological examination.
  • We suggested that hypothermia in the extremities may be added as a rare finding to the list of the clinical features in cervical myelopathy.
  • [MeSH-major] Hemangioma, Cavernous / complications. Hypothermia / etiology. Spinal Cord Neoplasms / complications

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  • (PMID = 19016121.001).
  • [ISSN] 1360-046X
  • [Journal-full-title] British journal of neurosurgery
  • [ISO-abbreviation] Br J Neurosurg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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48. Arai E, Kuramochi A, Tsuchida T, Tsuneyoshi M, Kage M, Fukunaga M, Ito T, Tada T, Izumi M, Shimizu K, Hirose T, Shimizu M: Usefulness of D2-40 immunohistochemistry for differentiation between kaposiform hemangioendothelioma and tufted angioma. J Cutan Pathol; 2006 Jul;33(7):492-7
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  • [Title] Usefulness of D2-40 immunohistochemistry for differentiation between kaposiform hemangioendothelioma and tufted angioma.
  • Our objective was to elucidate, using D2-40 immunohistochemistry, the differences among capillary hemangiomas, and especially between kaposiform hemangioendothelioma (KHE) and tufted angioma (TA).
  • In addition, the difference of immunostaining pattern of D2-40 is limited to the peripheral area of capillary proliferation and surrounding dilated vessels; therefore, it is suggested that KHE and TA may reflect different stages in the evolution of a single entity.
  • [MeSH-major] Antibodies, Monoclonal / immunology. Biomarkers, Tumor / immunology. Hemangioendothelioma / diagnosis. Hemangioma / diagnosis. Sarcoma, Kaposi / diagnosis. Skin Neoplasms / diagnosis
  • [MeSH-minor] Antibodies, Monoclonal, Murine-Derived. Capillaries. Diagnosis, Differential. Humans. Immunohistochemistry. Retrospective Studies


49. Al-Za'abi AM, Ghazarian D, Greenberg GR, Shaw JC: Eruptive tufted angiomas in a patient with Crohn's disease. J Clin Pathol; 2005 Feb;58(2):214-6
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  • [Title] Eruptive tufted angiomas in a patient with Crohn's disease.
  • Angioblastoma is a rare, benign vascular tumour composed of undifferentiated mesenchymal cells with a tendency to form lumina.
  • This entity was first described by Nakagawa in 1949 as angioblastoma, and Wilson Jones was the first to use the term "tufted angioma" in 1976.
  • Tufted angiomas usually occur in infancy and spread slowly.
  • This report describes lesions from the right side of the forehead, forearms, and thighs of a 24 year old man with a four year history of Crohn's disease, who was receiving infliximab in addition to long standing azathioprine and ciprofloxacillin.
  • He developed numerous small itchy erythematous vascular appearing papules, which on histological examination resembled tufted angiomas, showing the classic "cannon ball" appearance.
  • This case may represent an eruptive acquired tufted angioma in which immunosuppression or drug induced modification of angiogenesis played a role in its development and regression.
  • One previous case of eruptive tufted angioma has been reported in an immunosuppressed patient.
  • [MeSH-major] Crohn Disease / pathology. Hemangioma / pathology. Skin Neoplasms / pathology

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  • [Cites] Dermatology. 2000;201(1):68-70 [10971067.001]
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  • (PMID = 15677546.001).
  • [ISSN] 0021-9746
  • [Journal-full-title] Journal of clinical pathology
  • [ISO-abbreviation] J. Clin. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antibodies, Monoclonal; 0 / Gastrointestinal Agents; B72HH48FLU / Infliximab
  • [Other-IDs] NLM/ PMC1770572
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50. Ilknur T, Fetil E, Akarsu S, Altiner DD, Ulukuş C, Güneş AT: Angioma serpiginosum: dermoscopy for diagnosis, pulsed dye laser for treatment. J Dermatol; 2006 Apr;33(4):252-5
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  • [Title] Angioma serpiginosum: dermoscopy for diagnosis, pulsed dye laser for treatment.
  • Angioma serpiginosum is a rare benign vascular disorder, characterized clinically by multiple minute, red to purple, grouped macules in serpiginous and gyrate patterns and histopathologically by ectatic dilatation of capillaries.
  • An 18-year-old man with angioma serpiginosum of his left arm was evaluated by dermoscopy and treated with pulsed dye laser.
  • Our case supports the hypothesis that dermoscopy is beneficial in the diagnosis of angioma serpiginosum and that pulsed dye laser is effective in the treatment of this disorder.
  • [MeSH-major] Hemangioma / pathology. Hemangioma / radiotherapy. Skin Neoplasms / pathology. Skin Neoplasms / radiotherapy

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  • (PMID = 16674788.001).
  • [ISSN] 0385-2407
  • [Journal-full-title] The Journal of dermatology
  • [ISO-abbreviation] J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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51. Sarikaya-Seiwert S, Gierga K, Wessalowski R, Steiger HJ, Hänggi D: Solitary spinal epidural cavernous angiomas in children presenting with acute neurological symptoms caused by hemorrhage. J Neurosurg Pediatr; 2010 Jan;5(1):89-93

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  • [Title] Solitary spinal epidural cavernous angiomas in children presenting with acute neurological symptoms caused by hemorrhage.
  • Spinal solitary epidural cavernous angiomas are rare benign vascular malformations, which occur even less frequently in children than in adults.
  • In this report the authors describe 2 children presenting with acute symptoms and neurological deficits caused by hemorrhage within solitary spinal epidural cavernous angiomas.
  • The histological examination of the lesions revealed the characteristic structures of a cavernous angioma with hemosiderin deposits and acute hemorrhage.
  • Review of the literature confirmed that spinal epidural cavernous angiomas are extremely rare in the pediatric patient population, described currently in only 2 instances, but without acute hemorrhage.
  • These cases suggest that epidural cavernous angiomas also have to be considered in the pediatric patient population in the differential diagnosis of intraspinal lesions with acute or progressive neurological symptoms.
  • [MeSH-major] Epidural Neoplasms / surgery. Hemangioma, Cavernous, Central Nervous System / surgery
  • [MeSH-minor] Adolescent. Cervical Vertebrae / pathology. Cervical Vertebrae / surgery. Child. Female. Hematoma, Epidural, Spinal / diagnosis. Hematoma, Epidural, Spinal / surgery. Humans. Laminectomy. Magnetic Resonance Imaging. Spinal Cord Compression / diagnosis. Spinal Cord Compression / surgery. Thoracic Vertebrae / pathology. Thoracic Vertebrae / surgery

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  • (PMID = 20043742.001).
  • [ISSN] 1933-0715
  • [Journal-full-title] Journal of neurosurgery. Pediatrics
  • [ISO-abbreviation] J Neurosurg Pediatr
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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52. Alberola FT, Betlloch I, Montero LC, Nortes IB, Martínez NL, Paz AM: Congenital tufted angioma: Case report and review of the literature. Dermatol Online J; 2010;16(5):2
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  • [Title] Congenital tufted angioma: Case report and review of the literature.
  • Tufted angiomas (TA) are rare benign vascular tumors of unknown pathogenesis.
  • Their clinical presentation is non-specific and characterized by bluish-erythmatous plaques or nodules.
  • The differential diagnosis includes infantile hemangiomas, congenital hemangiomas, kaposiform hemangioendothelioma and vascular malformations.
  • Tufted angiomas have a characteristic histology consisting of a proliferation of endothelial cells forming lobules with the typical "shotgun" distribution.
  • [MeSH-major] Hemangioma / congenital. Skin Neoplasms / congenital
  • [MeSH-minor] Diagnosis, Differential. Female. Humans. Infant

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  • (PMID = 20492819.001).
  • [ISSN] 1087-2108
  • [Journal-full-title] Dermatology online journal
  • [ISO-abbreviation] Dermatol. Online J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 24
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53. Boockvar JA, Stiefel M, Malhotra N, Dolinskas C, Dwyer-Joyce C, LeRoux PD: Dural cavernous angioma of the posterior sagittal sinus: case report. Surg Neurol; 2005 Feb;63(2):178-81; discussion 181
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  • [Title] Dural cavernous angioma of the posterior sagittal sinus: case report.
  • BACKGROUND: Extraaxial cavernous hemangiomas (cavernomas) are very rare lesions, and less than 20 descriptions of these lesions outside the middle fossa have been reported.
  • In this report, we describe a dural cavernous angioma involving the posterior sagittal sinus and discuss the clinical, radiological, operative, and histological features of this very uncommon lesion.
  • The histological features were consistent with cavernous angioma.
  • CONCLUSION: This report demonstrates that although extra axial cavernomas are quite rare, they must be included in the differential diagnosis of enhancing lesions along the posterior sagittal sinus.
  • [MeSH-major] Cavernous Sinus / surgery. Dura Mater / surgery. Hemangioma, Cavernous / diagnosis. Hemangioma, Cavernous / surgery. Meningeal Neoplasms / diagnosis. Meningeal Neoplasms / surgery
  • [MeSH-minor] Adult. Cerebral Angiography. Diagnosis, Differential. Humans. Magnetic Resonance Imaging. Male

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  • (PMID = 15680668.001).
  • [ISSN] 0090-3019
  • [Journal-full-title] Surgical neurology
  • [ISO-abbreviation] Surg Neurol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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54. Lee B, Chiu M, Soriano T, Craft N: Adult-onset tufted angioma: a case report and review of the literature. Cutis; 2006 Nov;78(5):341-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult-onset tufted angioma: a case report and review of the literature.
  • Tufted angiomas (TAs) are benign vascular tumors, primarily occurring on the trunk and extremities of children younger than 5 years.
  • [MeSH-major] Hemangioma / pathology. Lip Neoplasms / pathology. Skin Neoplasms / pathology


55. Suvajdzić N, Cemerikić-Martinović V, Saranović D, Petrović M, Popović M, Artiko V, Cupić M, Elezović I: Littoral-cell angioma as a rare cause of splenomegaly. Clin Lab Haematol; 2006 Oct;28(5):317-20
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  • [Title] Littoral-cell angioma as a rare cause of splenomegaly.
  • We report the case of a littoral-cell angioma of the spleen, a recently described benign vascular tumour, whose imaging and pathological characteristics have been discussed only by a few authors.
  • The diagnosis was made after elective splenectomy.
  • [MeSH-major] Hemangioma / complications. Splenic Neoplasms / complications. Splenomegaly / etiology

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  • (PMID = 16999722.001).
  • [ISSN] 0141-9854
  • [Journal-full-title] Clinical and laboratory haematology
  • [ISO-abbreviation] Clin Lab Haematol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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56. Stockman A, Boralevi F, Taïeb A, Léauté-Labrèze C: SACRAL syndrome: spinal dysraphism, anogenital, cutaneous, renal and urologic anomalies, associated with an angioma of lumbosacral localization. Dermatology; 2007;214(1):40-5
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  • [Title] SACRAL syndrome: spinal dysraphism, anogenital, cutaneous, renal and urologic anomalies, associated with an angioma of lumbosacral localization.
  • BACKGROUND: Publications concerning perineal infantile hemangiomas are scarce, and comprise no large series.
  • OBJECTIVE: Studying clinical features of hemangiomas of the perineal area, complications and associated malformations.
  • METHODS: Retrospective analysis of all hemangiomas localized in the perineal area, encountered at the Children's Hospital in Bordeaux from 1994.
  • RESULTS: Of 49 perineal hemangiomas (34 girls, 15 boys), 5 patients had accompanying malformation, mainly lipomyelomeningocele with tethered cord.
  • The superficial hemangiomas were more represented in males and presented sooner than the nodular counterpart.
  • CONCLUSION: Superficial perineal hemangiomas are more often complicated by ulceration, and are associated with developmental anomalies.
  • As a counterpart for the PHACE syndrome in facial hemangioma, we propose the acronym SACRAL for perineal hemangiomas: Spinal dysraphism, Anogenital anomalies, Cutaneous anomalies, Renal and urologic anomalies, associated with Angioma of Lumbosacral localization.
  • [MeSH-major] Anal Canal / abnormalities. Hemangioma / complications. Skin Abnormalities / complications. Spinal Dysraphism / complications. Urogenital Abnormalities / complications
  • [MeSH-minor] Diagnosis, Differential. Female. France / epidemiology. Humans. Incidence. Infant. Infant, Newborn. Lumbosacral Plexus. Male. Perineum. Retrospective Studies. Sex Distribution. Syndrome

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  • [CommentIn] Dermatology. 2007;215(4):360; author reply 360-1 [17911998.001]
  • (PMID = 17191046.001).
  • [ISSN] 1018-8665
  • [Journal-full-title] Dermatology (Basel, Switzerland)
  • [ISO-abbreviation] Dermatology (Basel)
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Switzerland
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57. Bounameaux H, Calza AM, de Tonnac N, La Scala G, Pittet-Cuenod B, Yilmaz H, Rüfenacht D: [Multidisciplinary management of angiomas]. Rev Med Suisse; 2010 Feb 10;6(235):287-8, 290-1
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Multidisciplinary management of angiomas].
  • [Transliterated title] Prise en charge multidisciplinaire des angiomes.
  • Angiomas are heterogenous vascular abnormalities, in terms of anatomy, biology and clinical course.
  • The present paper summarizes contemporary classification of angiomas and presents some principles of multidisciplinary approach as it is applied for the past fifteen years at the University Hospitals of Geneva.
  • [MeSH-major] Hemangioma / therapy
  • [MeSH-minor] Arteriovenous Malformations / diagnosis. Arteriovenous Malformations / therapy. Humans. Infant, Newborn. Infant, Newborn, Diseases / therapy. Interprofessional Relations. Klippel-Trenaunay-Weber Syndrome / diagnosis. Klippel-Trenaunay-Weber Syndrome / therapy

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  • (PMID = 20218177.001).
  • [ISSN] 1660-9379
  • [Journal-full-title] Revue médicale suisse
  • [ISO-abbreviation] Rev Med Suisse
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Switzerland
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58. Colović R, Suvajdzić N, Grubor N, Colović N, Terzić T: Atypical immunophenotype in a littoral cell angioma. Vojnosanit Pregl; 2009 Jan;66(1):63-5
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  • [Title] Atypical immunophenotype in a littoral cell angioma.
  • BACKGROUND: Littoral-cell angioma (LCA) is a recently described benign vascular tumor of the spleen, whose imaging and pathologic characteristics have been discussed only by a few authors.
  • CASE REPORT: We reported a 60-year-old male with moderate nodular splenomegaly with one large hypoechogenic solid lesion and mild thrombocytopenia in whom the diagnosis of LCA was made after the elective splenectomy.
  • Namely, histopathological and immunohistochemical data allowed a final diagnosis of classical LCA in spite of CD21 negativity.
  • CONCLUSION: Littoral-cell angioma is a very rare benign splenic neoplasm that should be considered in the differential diagnosis of multinodular splenomegaly, particularly if the patient has the signs of hypersplenism.
  • [MeSH-major] Hemangioma / pathology. Splenic Neoplasms / pathology

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  • (PMID = 19195267.001).
  • [ISSN] 0042-8450
  • [Journal-full-title] Vojnosanitetski pregled
  • [ISO-abbreviation] Vojnosanit Pregl
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Serbia
  • [Chemical-registry-number] 0 / Antigens, CD; 0 / Antigens, Differentiation, Myelomonocytic; 0 / CD68 antigen, human
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59. Stavrinou LC, Stranjalis G, Flaskas T, Sakas DE: Trigonal cavernous angioma: a short illustrated review. Acta Neurochir (Wien); 2009 Nov;151(11):1517-20
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  • [Title] Trigonal cavernous angioma: a short illustrated review.
  • METHODS: We performed a search of the literature of the last 30 years and identified all cases of intraventricular cavernous angiomas.
  • RESULTS: Of a total of 61 intraventricular cases, 13 were located in the trigone of the lateral ventricles.
  • We feel that this difference has received little attention in the international literature.
  • We discuss a possible pathogenetic mechanism for the presence of intracranial hypertension and address different aspects of diagnosis and treatment of this benign lesion.
  • CONCLUSIONS: Trigonal cavernomas are benign lesions that have an excellent outcome after radical excision.
  • [MeSH-major] Cerebral Ventricle Neoplasms / pathology. Cerebral Ventricle Neoplasms / physiopathology. Hemangioma, Cavernous, Central Nervous System / pathology. Hemangioma, Cavernous, Central Nervous System / physiopathology. Lateral Ventricles / pathology
  • [MeSH-minor] Cerebral Hemorrhage / etiology. Cerebral Hemorrhage / physiopathology. Diagnosis, Differential. Female. Humans. Hydrocephalus / etiology. Hydrocephalus / physiopathology. Intracranial Hypertension / etiology. Intracranial Hypertension / physiopathology. Magnetic Resonance Imaging. Middle Aged. Neurosurgical Procedures. Papilledema / etiology. Papilledema / physiopathology. Seizures / etiology. Seizures / physiopathology. Treatment Outcome

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  • (PMID = 19300903.001).
  • [ISSN] 0942-0940
  • [Journal-full-title] Acta neurochirurgica
  • [ISO-abbreviation] Acta Neurochir (Wien)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Austria
  • [Number-of-references] 23
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60. Chen JH, Wang KH, Hu CH, Chiu JS: Atypical angioma serpiginosum. Yonsei Med J; 2008 Jun 30;49(3):509-13
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  • [Title] Atypical angioma serpiginosum.
  • Angioma serpiginosum is an uncommon, acquired vascular nevoid disorder with capillary dilation and proliferation in the papillary dermis.
  • According to the clinical and pathological findings, we established a diagnosis of angioma serpiginosum.
  • [MeSH-major] Skin Diseases, Vascular / diagnosis. Telangiectasis / diagnosis
  • [MeSH-minor] Dermatologic Surgical Procedures. Female. Foot Diseases / diagnosis. Foot Diseases / surgery. Humans. Lasers, Dye / therapeutic use. Middle Aged. Skin / blood supply. Skin / pathology. Treatment Outcome

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  • (PMID = 18581605.001).
  • [ISSN] 0513-5796
  • [Journal-full-title] Yonsei medical journal
  • [ISO-abbreviation] Yonsei Med. J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2615349
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61. Caroli E, Acqui M, Trasimeni G, Di Stefano D, Ferrante L: A case of intraroot cauda equina cavernous angioma: clinical considerations. Spinal Cord; 2007 Apr;45(4):318-21
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  • [Title] A case of intraroot cauda equina cavernous angioma: clinical considerations.
  • CONCLUSION: Lumbar intradural cavernous angioma may present with sciatalgia, low-back pain, neurological deficit, or, more rarely with subarachnoid hemorrhage or hydrocephalus.
  • Sometimes the sacrifice of the spinal root is inevitable because, as in present case, the cavernous angioma is included in the nerve root.
  • These lesions are rare and benign lesions.
  • [MeSH-major] Cauda Equina / pathology. Hemangioma, Cavernous / diagnosis. Magnetic Resonance Imaging / methods. Spinal Cord Neoplasms / diagnosis
  • [MeSH-minor] Aged. Diagnosis, Differential. Humans. Male

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  • (PMID = 16896337.001).
  • [ISSN] 1362-4393
  • [Journal-full-title] Spinal cord
  • [ISO-abbreviation] Spinal Cord
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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62. Chong PK, Loo AV, Alagaratnam JV: Von Hippel angioma. Med J Malaysia; 2007 Oct;62(4):343-4
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  • [Title] Von Hippel angioma.
  • We report a three year follow up of a 35-year-old Indian gentleman who presented with sudden, painless blurring of left (L) eye vision with initial visual acuity (VA) of 6/60.
  • Fundoscopy revealed (L) vitreous haemorrhage and subsequently confirmed a (L) inferotemporal capillary haemangioma.
  • The adjacent area of capillary haemangioma was treated with barricade argon laser photocoagulation to prevent progression of exudative retinal detachment inferiorly.
  • Subsequent follow up showed mild regression of capillary haemangioma with maintenance of (L) eye vision at 6/9.
  • [MeSH-major] Hemangioma, Capillary / diagnosis. Vision Disorders / diagnosis. Visual Acuity. von Hippel-Lindau Disease / diagnosis

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  • (PMID = 18551944.001).
  • [ISSN] 0300-5283
  • [Journal-full-title] The Medical journal of Malaysia
  • [ISO-abbreviation] Med. J. Malaysia
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Malaysia
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63. Lenzi J, Seferi A, Nardone A, Salvati M, Vreto G, Santoro A, Raco A, Pichierri A, Petrela M: Sylvian subarachnoid and extra-pial cavernous angioma. J Neurosurg Sci; 2005 Dec;49(4):163-6; discussion 166
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  • [Title] Sylvian subarachnoid and extra-pial cavernous angioma.
  • Cavernous angiomas are one of the four types of vascular malformations of the central nervous system.
  • Our case represents an unusual localization of a subarachnoid cavernous angioma.
  • This case represents a radiologically visible supratentorial extra-pial subarachnoidal cavernous angioma.
  • [MeSH-major] Hemangioma, Cavernous / pathology. Subarachnoid Space / pathology. Supratentorial Neoplasms / pathology

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  • (PMID = 16374409.001).
  • [ISSN] 0390-5616
  • [Journal-full-title] Journal of neurosurgical sciences
  • [ISO-abbreviation] J Neurosurg Sci
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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64. Korotkikh NG, Ol'shanskiĭ MS, Shcherbinin AS, Stepanov IV, Alekseeva TV, Ovsiannikov IuM: [Endovascular microembolization of the posterior auricular artery in comprehensive surgical management of capillary angioma of the floor of the auricle]. Angiol Sosud Khir; 2007;13(4):74-6
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  • [Title] [Endovascular microembolization of the posterior auricular artery in comprehensive surgical management of capillary angioma of the floor of the auricle].
  • The article deals with the description of a rare clinical case wherein a 44-year-old female patient presenting with bleeding capillary angioma of the left auricle obstructing the auditory passage was fist subjected to endovascular microembolization of the posterior auricular artery by means of polyvinyl alcohol (PVA-500), followed by a second stage of virtually bloodlessly surgical removal of the tumour carried out five days thereafter.
  • This case report once again points to feasibility of combined, i. e. endovascular and conventional surgical management of capillary angiomas.
  • Preoperative microembolization of a bleeding haemangioma arrests haemorrhage from the tumour, resulting in the decreased size thereof, as well as leading to circumscribing the tumour from healthy tissue.
  • [MeSH-major] Ear Neoplasms / therapy. Ear, External / blood supply. Embolization, Therapeutic / methods. Hemangioma, Capillary / therapy

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  • (PMID = 18385652.001).
  • [ISSN] 1027-6661
  • [Journal-full-title] Angiologii︠a︡ i sosudistai︠a︡ khirurgii︠a︡ = Angiology and vascular surgery
  • [ISO-abbreviation] Angiol Sosud Khir
  • [Language] rus
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Russia (Federation)
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65. Kim HG, Park IS, Lee JI, Jeong S, Lee JW, Kwon KS, Lee DH, Kim PS, Kim HG, Shin YW, Kim YS, Ahn IS, Lee KY: Littoral cell angioma (LCA) associated with liver cirrhosis. Yonsei Med J; 2005 Feb 28;46(1):184-8
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  • [Title] Littoral cell angioma (LCA) associated with liver cirrhosis.
  • A littoral cell angioma (LCA) is a rare benign vascular tumor of the spleen.
  • A 60-year-old man, with multiple nodules in imaging study and liver cirrhosis graded as Child-Pugh classification class A, was transferred for splenomegaly.
  • Because there was no evidence of hematological and visceral malignancy, a splenectomy was performed for a definitive diagnosis.
  • There has been no previous report of a LCA combined with liver cirrhosis.
  • Herein, the first case of a LCA in Korea, diagnosed and treated by a splenectomy, is reported.
  • [MeSH-major] Hemangioma / complications. Liver Cirrhosis / complications. Splenic Neoplasms / complications

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  • [Cites] AJR Am J Roentgenol. 1999 Apr;172(4):933-7 [10587123.001]
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  • (PMID = 15744827.001).
  • [ISSN] 0513-5796
  • [Journal-full-title] Yonsei medical journal
  • [ISO-abbreviation] Yonsei Med. J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2823050
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66. Le Huu AR, Jokinen CH, Rubin BP, Mihm MC, Weiss SW, North PE, Dadras SS: Expression of prox1, lymphatic endothelial nuclear transcription factor, in Kaposiform hemangioendothelioma and tufted angioma. Am J Surg Pathol; 2010 Nov;34(11):1563-73
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Expression of prox1, lymphatic endothelial nuclear transcription factor, in Kaposiform hemangioendothelioma and tufted angioma.
  • Kaposiform hemangioendothelioma (KHE) and tufted angioma (TA) are rare tumors mainly occurring in early childhood.
  • For this purpose, we examined 75 vascular lesions: KHE (n=18), TA (n=13), infantile hemangioma (n=13), pyogenic granuloma (n=18), and granulation tissue (n=13).
  • The lesional cells of all infantile hemangiomas and pyogenic granulomas were negative for Prox1 in the presence of positive internal control.
  • Overall, our results show, for the first time, that Prox1 is an immunohistochemical biomarker helpful in confirming the diagnosis of KHE/TA and in distinguishing it from infantile hemangioma and pyogenic granuloma.
  • [MeSH-major] Biomarkers, Tumor / analysis. Hemangioendothelioma / chemistry. Hemangioma / chemistry. Homeodomain Proteins / analysis. Skin Neoplasms / chemistry. Soft Tissue Neoplasms / chemistry. Tumor Suppressor Proteins / analysis
  • [MeSH-minor] Adolescent. Antigens, CD31 / analysis. Antigens, CD34 / analysis. Cell Nucleus / chemistry. Child. Child, Preschool. Cytoplasm / chemistry. Diagnosis, Differential. Granuloma, Pyogenic / metabolism. Humans. Immunohistochemistry. Immunophenotyping. Infant. Membrane Glycoproteins / analysis. Predictive Value of Tests. Vesicular Transport Proteins / analysis

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  • [ErratumIn] Am J Surg Pathol. 2011 Feb;35(2):314. Ruben, Brian P [corrected to Rubin, Brian P]
  • (PMID = 20975337.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD31; 0 / Antigens, CD34; 0 / Biomarkers, Tumor; 0 / Homeodomain Proteins; 0 / LYVE1 protein, human; 0 / Membrane Glycoproteins; 0 / PDPN protein, human; 0 / Tumor Suppressor Proteins; 0 / Vesicular Transport Proteins; 0 / prospero-related homeobox 1 protein
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67. Zakaria MA, Abdullah JM, George JP, Mutum SS, Lee NN: Third ventricular cavernous angioma. Med J Malaysia; 2006 Jun;61(2):229-32
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  • [Title] Third ventricular cavernous angioma.
  • Third ventricular cavernous angiomas are rare vascular malformations of the brain.
  • We report an eight-year old boy with a rare third ventricular cavernous angioma that hemorrhaged presenting with symptoms of acute hydrocephalus.
  • [MeSH-major] Central Nervous System Neoplasms / diagnosis. Hemangioma, Cavernous, Central Nervous System / diagnosis. Third Ventricle
  • [MeSH-minor] Child. Diagnosis, Differential. Follow-Up Studies. Humans. Magnetic Resonance Imaging. Male. Tomography, X-Ray Computed

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  • (PMID = 16898318.001).
  • [ISSN] 0300-5283
  • [Journal-full-title] The Medical journal of Malaysia
  • [ISO-abbreviation] Med. J. Malaysia
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Malaysia
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68. Ohba S, Shimizu K, Shibao S, Nakagawa T, Murakami H: Cystic cavernous angiomas. Neurosurg Rev; 2010 Oct;33(4):395-400
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  • [Title] Cystic cavernous angiomas.
  • Cystic cavernous angiomas are rarely found in patients.
  • We have reviewed 25 cases of cystic cavernous angiomas, including our case.
  • The cystic cavernous angiomas were located in the supratentorial region in 16 (64%) cases, the cerebellopontine angle in 4 (16%) cases, and the cerebellum in 5 (20%) cases.
  • [MeSH-major] Brain Neoplasms / surgery. Central Nervous System Cysts / surgery. Hemangioma, Cavernous / surgery

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  • (PMID = 20174956.001).
  • [ISSN] 1437-2320
  • [Journal-full-title] Neurosurgical review
  • [ISO-abbreviation] Neurosurg Rev
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Germany
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69. Bi CF, Jiang LL, Li Z, Liu WP: [Littoral cell angioma of spleen: a clinicopathologic study of 17 cases]. Zhonghua Bing Li Xue Za Zhi; 2007 Apr;36(4):239-43
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Littoral cell angioma of spleen: a clinicopathologic study of 17 cases].
  • OBJECTIVE: To study the clinicopathologic features and immunophenotype of splenic littoral cell angioma.
  • METHODS: The clinical features, radiologic findings and histopathology of 17 cases of splenic littoral cell angioma were retrospectively reviewed.
  • Immunohistochemical study was carried out on paraffin-embedded tissues, using normal spleen, cases of congestive splenomegaly and cavernous hemangioma as controls.
  • The immunophenotype of splenic littoral cell angioma was different from that of the controls.
  • CONCLUSIONS: Littoral cell angioma is a benign condition, likely secondary to hemodynamic disturbance in spleen.
  • The littoral cells become hyperplastic and anastomose, resulting in a hemangioma-like growth associated with histiocytic reaction.
  • Attention to the characteristic histopathologic findings and immunophenotype are crucial for diagnosis.
  • [MeSH-major] Antigens, CD31 / metabolism. Hemangioma / pathology. Spleen / pathology. Splenic Neoplasms / pathology
  • [MeSH-minor] Adult. Aged. Antigens, CD / metabolism. Antigens, Differentiation, Myelomonocytic / metabolism. Diagnosis, Differential. Female. Follow-Up Studies. Hemangioma, Cavernous / immunology. Hemangioma, Cavernous / pathology. Humans. Immunohistochemistry. Male. Middle Aged. Receptors, Cell Surface / metabolism. Retrospective Studies. Splenomegaly / metabolism. Splenomegaly / pathology. von Willebrand Factor / metabolism

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  • (PMID = 17706114.001).
  • [ISSN] 0529-5807
  • [Journal-full-title] Zhonghua bing li xue za zhi = Chinese journal of pathology
  • [ISO-abbreviation] Zhonghua Bing Li Xue Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] 0 / Antigens, CD; 0 / Antigens, CD31; 0 / Antigens, Differentiation, Myelomonocytic; 0 / CD163 antigen; 0 / CD68 antigen, human; 0 / Receptors, Cell Surface; 0 / von Willebrand Factor
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70. Mohan V, Jones RC, Drake AJ 3rd, Daly PL, Shakir KM: Littoral cell angioma presenting as metastatic thyroid carcinoma to the spleen. Thyroid; 2005 Feb;15(2):170-5
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  • [Title] Littoral cell angioma presenting as metastatic thyroid carcinoma to the spleen.
  • This is the case of a 25-year-old man with a history of PTC (1.4 cm primary; no capsular invasion and negative lymph node metastases).
  • One year after initial surgery, recurrent disease was found in multiple neck nodes by central neck dissection.
  • Computerized axial tomography (CT) of the chest one year later showed no gross mediastinal or pulmonary disease.
  • Despite the serum thyroglobulin of only 9.4 ng/mL, the finding of I(131) accumulation within solid splenic masses led to a preoperative diagnosis of thyroid carcinoma metastases.
  • To establish the diagnosis and to remove the risk for splenic rupture, a laparoscopic splenectomy was performed.
  • Histopathologic analysis showed large littoral cell angiomas (LCA).
  • False-positive radioiodine scintigraphy in the setting of PTC involving a vertebral hemangioma has been reported.
  • To our knowledge, this is the first case that describes multiple angiomas mimicking metastatic thyroid carcinoma to the spleen.
  • [MeSH-major] Carcinoma, Papillary / secondary. Hemangioma / pathology. Splenic Neoplasms / secondary. Thyroid Neoplasms / pathology
  • [MeSH-minor] Adult. Diagnosis, Differential. False Positive Reactions. Female. Humans. Iodine Radioisotopes. Tomography, X-Ray Computed. Ultrasonography, Doppler

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  • (PMID = 15753678.001).
  • [ISSN] 1050-7256
  • [Journal-full-title] Thyroid : official journal of the American Thyroid Association
  • [ISO-abbreviation] Thyroid
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Iodine Radioisotopes
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71. Bayramgurler D, Filinte D, Kiran R: Angioma serpiginosum with sole involvement. Eur J Dermatol; 2008 Nov-Dec;18(6):708-9
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  • [Title] Angioma serpiginosum with sole involvement.
  • Angioma serpiginosum, which is characterized by multiple, minute, angiomatous puncta, is mainly located on the lower extremities of girls under the age of 16.
  • Increased levels of estrogens have been proposed in the development of angioma serpiginosum.
  • [MeSH-major] Foot Diseases / pathology. Skin Diseases, Vascular / pathology

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  • (PMID = 18955205.001).
  • [ISSN] 1167-1122
  • [Journal-full-title] European journal of dermatology : EJD
  • [ISO-abbreviation] Eur J Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
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72. Lin CH, Yu JC, Shih ML, Peng YJ, Hsieh CB: Littoral cell angioma of the spleen in a patient with hepatocellular carcinoma. J Formos Med Assoc; 2005 Apr;104(4):282-5
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  • [Title] Littoral cell angioma of the spleen in a patient with hepatocellular carcinoma.
  • Littoral cell angioma (LCA) is a rare primitive vascular tumor of the spleen which is benign and usually associated with visceral malignancy.
  • The diagnosis of LCA is based on histologic and immunohistologic analysis.
  • Histopathology showed a moderately differentiated HCC of the liver and splenic angioma with dilated vascular channels lined by plump endothelial cells.

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  • (PMID = 15909068.001).
  • [ISSN] 0929-6646
  • [Journal-full-title] Journal of the Formosan Medical Association = Taiwan yi zhi
  • [ISO-abbreviation] J. Formos. Med. Assoc.
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Singapore
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73. Yagi K, Kageji T, Nagahiro S, Murayama Y: Multiple cystic cavernous angiomas associated with hemorrhage. Acta Neurochir (Wien); 2005 Feb;147(2):201-3; discussion 203

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  • [Title] Multiple cystic cavernous angiomas associated with hemorrhage.
  • The histological diagnosis was cavernous angioma.
  • The first report of multiple cystic cavernous angiomas is reported.
  • [MeSH-major] Brain / pathology. Central Nervous System Cysts / complications. Cerebral Hemorrhage / etiology. Cerebral Hemorrhage / pathology. Hemangioma, Cavernous, Central Nervous System / complications. Hemangioma, Cavernous, Central Nervous System / pathology
  • [MeSH-minor] Adult. Calcinosis / etiology. Calcinosis / pathology. Calcinosis / radiography. Craniotomy. Diagnosis, Differential. Humans. Magnetic Resonance Imaging. Male. Memory Disorders / etiology. Memory Disorders / pathology. Memory Disorders / radiography. Neurocysticercosis / diagnosis. Tomography, X-Ray Computed

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  • (PMID = 15365796.001).
  • [ISSN] 0001-6268
  • [Journal-full-title] Acta neurochirurgica
  • [ISO-abbreviation] Acta Neurochir (Wien)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Austria
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74. Erçin C, Gürbüz Y, Hacihanefioğlu A, Turgut Karakaya A: Multiple littoral cell angioma of the spleen in a case of myelodysplastic syndrome. Hematology; 2005 Apr;10(2):141-4
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  • [Title] Multiple littoral cell angioma of the spleen in a case of myelodysplastic syndrome.
  • Littoral cell angioma (LCA) of the spleen is a relatively recently described rare entity, which is associated with haemophagocytosis.
  • The patient presented with pancytopenia and multiple haemangiomas were observed in spleen during diagnostic abdominal ultrasound.
  • As LCA of the spleen and myelodysplastic syndrome may both cause cytopenia their co-existence may complicate the clinical presentation leading to an incomplete or inappropriate diagnosis.
  • In cases of haematological disorders with an atypical course, the radiological examination of the spleen should be considered and the possibility of angiomas must be included to the differential diagnosis.
  • [MeSH-major] Hemangioma / pathology. Myelodysplastic Syndromes / pathology. Splenic Neoplasms / pathology

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  • (PMID = 16019460.001).
  • [ISSN] 1024-5332
  • [Journal-full-title] Hematology (Amsterdam, Netherlands)
  • [ISO-abbreviation] Hematology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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75. Dong MJ, Zhou GY: [Imaging diagnosis of hemangioma in infants]. Shanghai Kou Qiang Yi Xue; 2008 Apr;17(2):221-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Imaging diagnosis of hemangioma in infants].
  • Hemangioma is the most commonly benign tumor of soft tissue tumors in infants.
  • In this article, the current situation of application with all imaging examinations used in diagnosis of hemangioma is reviewed.
  • [MeSH-major] Hemangioma / diagnosis

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  • (PMID = 18470434.001).
  • [ISSN] 1006-7248
  • [Journal-full-title] Shanghai kou qiang yi xue = Shanghai journal of stomatology
  • [ISO-abbreviation] Shanghai Kou Qiang Yi Xue
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
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76. Kazim SF, Bhatti, Enam SA: Intracranial cavernous angiomas. J Coll Physicians Surg Pak; 2010 Nov;20(11):738-43
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Intracranial cavernous angiomas.
  • OBJECTIVE: To describe the clinical presentation, diagnosis, and management of patients presenting with intracranial cavernous angiomas (CAs) at a tertiary care hospital in Pakistan.
  • The studied variables included patient demographics, clinical presentation, family history of intracranial CAs or other space occupying lesions, modality of diagnosis, management, and outcome.
  • The median age at diagnosis was 28.5 years.
  • The outcome was satisfactory except for one patient, who died within 6 months of diagnosis.
  • This data raises a possibility of a higher frequency of multiple cavernomas in Pakistani patients.
  • [MeSH-major] Brain Neoplasms / surgery. Hemangioma, Cavernous / surgery

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  • (PMID = 21078247.001).
  • [ISSN] 1022-386X
  • [Journal-full-title] Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
  • [ISO-abbreviation] J Coll Physicians Surg Pak
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Pakistan
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77. Gianfrancesco F, Cannella M, Martino T, Maglione V, Esposito T, Innocenzi G, Vitale E, Liquori CL, Marchuk DA, Squitieri F: Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations. Am J Med Genet B Neuropsychiatr Genet; 2007 Jul 5;144B(5):691-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations.
  • In most cases, cerebral cavernous malformations (CCMs) involve the brain alone, and are rarely associated with skin hemangiomas, spinal cord, retinal, hepatic or vertebral lesions.
  • After collecting CCM families of Italian origin and investigating the genetic basis of the disorder we disclosed two novel molecular variations in the KRIT1 and MGC4607 genes.
  • We found a novel CCM1 gene mutation (Q66X) in a family with apparently asymptomatic old-aged mutation carriers and patients who either had skin angiomas alone or the full association of cerebral, spinal, and skin lesions.
  • [MeSH-major] Carrier Proteins / genetics. Hemangioma, Cavernous, Central Nervous System / genetics. Microtubule-Associated Proteins / genetics. Mutation. Penetrance. Proto-Oncogene Proteins / genetics

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  • (PMID = 17440989.001).
  • [ISSN] 1552-4841
  • [Journal-full-title] American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
  • [ISO-abbreviation] Am. J. Med. Genet. B Neuropsychiatr. Genet.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / CCM2 protein, human; 0 / Carrier Proteins; 0 / KRIT1 protein, human; 0 / Microtubule-Associated Proteins; 0 / Proto-Oncogene Proteins
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78. Mühlfeld AS, Eitner F, Perez-Bouza A, Knuechel R, Heintz B, Floege J: Littoral cell angioma of the spleen mimicking posttransplantation lymphoma in a 63-year-old renal transplant patient. Am J Kidney Dis; 2008 Sep;52(3):e11-4
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  • [Title] Littoral cell angioma of the spleen mimicking posttransplantation lymphoma in a 63-year-old renal transplant patient.
  • Littoral cell angiomas are benign vascular tumors originating from the littoral cells lining the splenic sinuses.
  • In this report, we describe the case of a 63-year-old patient who developed night sweats 16 months after renal transplantation.
  • Histological examination of the pathological specimen from the splenectomy specimen showed multiple littoral cell angiomas of the spleen.
  • More specific tools need to be developed to aid in the differential diagnosis of splenic masses to avoid splenectomy in patients with littoral cell angiomas.
  • [MeSH-major] Hemangioma / diagnosis. Kidney Transplantation / adverse effects. Lymphoma / diagnosis. Lymphoma / etiology. Neoplasms, Second Primary / diagnosis. Splenic Neoplasms / diagnosis
  • [MeSH-minor] Diagnosis, Differential. Humans. Male. Middle Aged. Spleen / pathology. Spleen / radiography. Tomography, X-Ray Computed

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  • (PMID = 18479795.001).
  • [ISSN] 1523-6838
  • [Journal-full-title] American journal of kidney diseases : the official journal of the National Kidney Foundation
  • [ISO-abbreviation] Am. J. Kidney Dis.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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79. Yamate J, Izawa T, Kuwamura M, Mitsunaga F, Nakamura S: Vasoformative disorder, resembling littoral cell angioma, of the spleen in a geriatric Japanese macaque (Macaca fuscata). Vet Pathol; 2009 May;46(3):520-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Vasoformative disorder, resembling littoral cell angioma, of the spleen in a geriatric Japanese macaque (Macaca fuscata).
  • The enlarged spleen consisted of neoplastic proliferation of anastomosing vascular channels resembling morphologic structures of red pulp sinuses; occasionally, papillary fronds were seen in dilated channels.
  • Based on the pathologic characteristics, particularly the presence of neoplastic cells with macrophage/histiocyte-like attributes, this tumor was regarded as littoral cell angioma; this is a rare benign splenic vascular tumor.
  • [MeSH-major] Hemangioma / veterinary. Macaca. Monkey Diseases / pathology. Splenic Neoplasms / veterinary

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  • (PMID = 19176500.001).
  • [ISSN] 0300-9858
  • [Journal-full-title] Veterinary pathology
  • [ISO-abbreviation] Vet. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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80. Johnson C, Goyal M, Kim B, Wasdahl D, Nazinitsky K: Littoral cell angioma. Clin Imaging; 2007 Jan-Feb;31(1):27-31
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Littoral cell angioma.
  • Littoral cell angioma (LCA) is an extremely rare primary splenic tumor.
  • [MeSH-major] Erythrocytes / radionuclide imaging. Hemangioma / diagnosis. Hemangioma / surgery. Splenic Neoplasms / diagnosis. Splenic Neoplasms / surgery. Technetium
  • [MeSH-minor] Diagnosis, Differential. Female. Humans. Magnetic Resonance Imaging. Middle Aged. Radiopharmaceuticals. Rare Diseases / diagnosis. Tomography, X-Ray Computed. Treatment Outcome. Ultrasonography

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  • (PMID = 17189843.001).
  • [ISSN] 0899-7071
  • [Journal-full-title] Clinical imaging
  • [ISO-abbreviation] Clin Imaging
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Radiopharmaceuticals; 7440-26-8 / Technetium
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81. Prada F, Saladino A, Giombini S: Trigonal cavernous angioma presenting with selective ventricular exclusion. J Neurosurg Sci; 2010 Dec;54(4):153-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Trigonal cavernous angioma presenting with selective ventricular exclusion.
  • We present a case of a patient with an intraventricular cavernous angioma originating from the splenium of the corpus callosum presenting with intracranial hypertension syndrome.
  • [MeSH-major] Brain Neoplasms / pathology. Corpus Callosum / pathology. Hemangioma, Cavernous / pathology. Occipital Lobe / pathology. Temporal Lobe / pathology
  • [MeSH-minor] Adult. Female. Humans. Intracranial Hypertension / diagnosis. Magnetic Resonance Imaging. Neurosurgical Procedures. Tomography, X-Ray Computed. Treatment Outcome

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  • (PMID = 21423086.001).
  • [ISSN] 0390-5616
  • [Journal-full-title] Journal of neurosurgical sciences
  • [ISO-abbreviation] J Neurosurg Sci
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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82. Qu ZB, Liu LX, Wu LF, Zhao S, Jiang HC: Multiple littoral cell angioma of the spleen: a case report and review of the literature. Onkologie; 2007 May;30(5):256-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple littoral cell angioma of the spleen: a case report and review of the literature.
  • BACKGROUND: Littoral cell angioma (LCA) is a rare benign vascular tumor of the spleen with characteristic histomorphologic features.
  • It is a unique splenic tumor which may present with abdominal pain or as an incidental finding.
  • CASE REPORT: In this case report, we present the case of a 34-year-old woman with multiple splenic LCA.
  • After a diagnostic abdominal ultrasound, multiple hemangiomas were observed in the spleen.
  • Postoperative histological and immunohistochemical profiles confirmed the diagnosis of LCA.
  • CONCLUSION: LCA is a unique splenic tumor diagnosed in patients with abdominal pain or as an incidental finding.
  • [MeSH-major] Hemangioma / surgery. Neoplasms, Multiple Primary / surgery. Splenic Neoplasms / surgery

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  • (PMID = 17460421.001).
  • [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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83. Cosme A, Tejada A, Bujanda L, Vaquero M, Elorza JL, Ojeda E, Goikoetxea U: Littoral-cell angioma of the spleen: a case report. World J Gastroenterol; 2007 Dec 28;13(48):6603-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Littoral-cell angioma of the spleen: a case report.
  • Littoral-cell angioma (LCA) is a primary splenic vascular tumor that arises from the normal littoral cells lining the sinus channels of the splenic red pulp.
  • LCA is a benign vascular tumor of the spleen that needs to be included in the differential diagnosis of multiple splenic nodules.
  • [MeSH-major] Hemangioma / diagnosis. Hemangioma / pathology. Splenic Neoplasms / diagnosis. Splenic Neoplasms / pathology

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  • (PMID = 18161935.001).
  • [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
  • [Chemical-registry-number] 0 / Antigens, CD; 0 / Antigens, CD31; 0 / Antigens, Differentiation, Myelomonocytic; 0 / Biomarkers; 0 / CD68 antigen, human
  • [Other-IDs] NLM/ PMC4611304
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84. Puso C, Guillot B, Durand L, Guilhou JJ, Bessis D: [Capillary malformations associated with cerebral cavernous malformation]. Ann Dermatol Venereol; 2005 May;132(5):471-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Transliterated title] Malformations capillaires associées à un angiome caverneux cérébral.
  • INTRODUCTION: Capillary malformations such as benign hereditary telangiectasia are a familial affection, of dominant autosomal transmission, characterized by the progressive development of cutaneous telangiectasia during childhood.
  • The familial history of telangiectasic macules and clinical and histological examination led to the diagnosis of benign hereditary telangiectasia.
  • DISCUSSION: This case report raises doubt on the exclusively cutaneous nature of benign hereditary telangiectasic-type capillary malformations.
  • Moreover, it illustrates the possibility of a particular clinical form of this affection, associating classical telangiectasia and post-wine stain-type macules.
  • The recent localization of the locus implied in this affection in 5q14 in the same chromosomic space as the CMC1 locus incriminated in familial capillary malformations, suggests that these two affections are in fact phenotype variations of a single and same clinical entity.
  • [MeSH-major] Central Nervous System Vascular Malformations / complications. Central Nervous System Vascular Malformations / pathology. Hemangioma, Cavernous / complications. Hemangioma, Cavernous / pathology

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  • (PMID = 15988361.001).
  • [ISSN] 0151-9638
  • [Journal-full-title] Annales de dermatologie et de vénéréologie
  • [ISO-abbreviation] Ann Dermatol Venereol
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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85. Cai C, Böttcher MC, Werner JA, Mandic R: Differential expression of VEGF121, VEGF165 and VEGF189 in angiomas and squamous cell carcinoma cell lines of the head and neck. Anticancer Res; 2010 Mar;30(3):805-10
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Differential expression of VEGF121, VEGF165 and VEGF189 in angiomas and squamous cell carcinoma cell lines of the head and neck.
  • To determine the expression of VEGF isoforms in angioma and head and neck squamous cell carcinoma (HNSCC), both being dependent on pathological neovascularization, we included 11 HNSCC cell lines, 4 hemangiomas and 5 vascular malformations (VMs) in the study.
  • Interestingly, VMs expressed significantly higher (p=0.0286) amounts of VEGF(121) compared with hemangiomas, which had levels similar to normal control mucosa.
  • One drawback of this study was the small number of specimens available, particularly since VMs and hemangiomas are relatively rare diseases.
  • Future studies need to follow-up on these observations and further evaluate the potential role of specific VEGF isoforms in the pathogenesis of hemangioma and VM.
  • [MeSH-major] Carcinoma, Squamous Cell / metabolism. Head and Neck Neoplasms / metabolism. Hemangioma / metabolism. Vascular Endothelial Growth Factor A / biosynthesis

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  • (PMID = 20393000.001).
  • [ISSN] 1791-7530
  • [Journal-full-title] Anticancer research
  • [ISO-abbreviation] Anticancer Res.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Greece
  • [Chemical-registry-number] 0 / Protein Isoforms; 0 / VEGFA protein, human; 0 / Vascular Endothelial Growth Factor A
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86. Ramesh R, De Silva B, Atherton DJ: Congenital tufted angioma with persistent low-grade coagulopathy. Clin Exp Dermatol; 2009 Dec;34(8):e766-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Congenital tufted angioma with persistent low-grade coagulopathy.
  • A female infant, born with a tufted angioma, developed a coagulopathy with prolonged bleeding time, with the risk of progression to Kasabach-Merritt phenomenon.
  • We opted for a conservative approach of observation, which was vindicated by the outcome.
  • [MeSH-major] Hemangioma / pathology. Skin Neoplasms / pathology

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  • (PMID = 19778314.001).
  • [ISSN] 1365-2230
  • [Journal-full-title] Clinical and experimental dermatology
  • [ISO-abbreviation] Clin. Exp. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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87. Osio A, Fraitag S, Hadj-Rabia S, Bodemer C, de Prost Y, Hamel-Teillac D: Clinical spectrum of tufted angiomas in childhood: a report of 13 cases and a review of the literature. Arch Dermatol; 2010 Jul;146(7):758-63
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Clinical spectrum of tufted angiomas in childhood: a report of 13 cases and a review of the literature.
  • BACKGROUND: Tufted angioma (TA) is a rare benign vascular tumor that mostly appears during infancy or early childhood.
  • Histologic tufts of capillaries infiltrating the whole dermis in a "cannonball" distribution pattern associated with dilated lymphatic vessels are characteristic of the disease and confirm the diagnosis.
  • Few case series of TA have been published, and the morphologic structure and evolution of TA seem to vary.
  • [MeSH-major] Hemangioma / pathology. Skin / pathology. Skin Neoplasms / pathology
  • [MeSH-minor] Adolescent. Child. Child, Preschool. Diagnosis, Differential. Female. Follow-Up Studies. Humans. Male. Retrospective Studies. Young Adult

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  • (PMID = 20644037.001).
  • [ISSN] 1538-3652
  • [Journal-full-title] Archives of dermatology
  • [ISO-abbreviation] Arch Dermatol
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] United States
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88. Kreusel KM, Bechrakis NE, Neumann HP, Foerster MH: Pars plana vitrectomy for juxtapapillary capillary retinal angioma. Am J Ophthalmol; 2006 Mar;141(3):587-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Pars plana vitrectomy for juxtapapillary capillary retinal angioma.
  • PURPOSE: To describe the treatment of juxtapapillary capillary angioma by pars plana vitrectomy (PPV) and tumor excision.
  • METHODS: A 6-year-old girl with symptomatic juxtapapillary capillary retinal angioma with associated epiretinal membrane (ERM) underwent PPV and extraction of the tumor and ERM.
  • A clinical and molecular genetic workup for the presence of von Hippel-Lindau disease (VHL) was performed.
  • Capillary retinal angioma was confirmed by histology of the surgical specimen, and familial VHL was revealed.
  • CONCLUSIONS: PPV and extraction of the tumor is applicable in juxtapapillary capillary retinal angioma with associated ERM.
  • [MeSH-major] Hemangioma, Capillary / surgery. Retinal Neoplasms / surgery. Vitrectomy / methods
  • [MeSH-minor] Child. Epiretinal Membrane / pathology. Epiretinal Membrane / surgery. Female. Fluorescein Angiography. Humans. Visual Acuity. Von Hippel-Lindau Tumor Suppressor Protein / genetics. von Hippel-Lindau Disease / genetics

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  • (PMID = 16490522.001).
  • [ISSN] 0002-9394
  • [Journal-full-title] American journal of ophthalmology
  • [ISO-abbreviation] Am. J. Ophthalmol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] EC 6.3.2.19 / VHL protein, human; EC 6.3.2.19 / Von Hippel-Lindau Tumor Suppressor Protein
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89. Capelle HH, Nakamura M, Lenarz T, Brandis A, Haubitz B, Krauss JK: Cavernous angioma of the geniculate ganglion. J Neurosurg; 2008 Nov;109(5):893-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cavernous angioma of the geniculate ganglion.
  • Intracranial extraaxial cavernous angiomas are rare vascular malformations.
  • Histological examination revealed a cavernous angioma.
  • [MeSH-major] Cranial Nerve Neoplasms / diagnosis. Geniculate Ganglion. Hemangioma, Cavernous / diagnosis
  • [MeSH-minor] Adult. Facial Paralysis / diagnosis. Facial Paralysis / etiology. Humans. Male

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  • (PMID = 18976080.001).
  • [ISSN] 0022-3085
  • [Journal-full-title] Journal of neurosurgery
  • [ISO-abbreviation] J. Neurosurg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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90. Wu MC, Luo SQ, Xie J, Ma ZY, Zhang YQ, Jia G: [Supratentorial cavernous angiomas in children]. Zhonghua Yi Xue Za Zhi; 2006 Feb 7;86(5):329-31

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Supratentorial cavernous angiomas in children].
  • OBJECTIVE: To discuss the clinical features, treatment, and prognosis of supratentorial cavernous angiomas in children.
  • METHODS: The clinical data of 25 pediatric patients with supratentorial cavernous angioma, 17 boys and 6 girls, aged 9.6 (1-15), were reviewed retrospectively, and the relationship between the duration of epilepsy before surgery and prognosis was analyzed.
  • [MeSH-major] Hemangioma, Cavernous, Central Nervous System / surgery. Supratentorial Neoplasms / surgery

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  • (PMID = 16677527.001).
  • [ISSN] 0376-2491
  • [Journal-full-title] Zhonghua yi xue za zhi
  • [ISO-abbreviation] Zhonghua Yi Xue Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
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91. Hara S: Venous angioma in an airman. Aviat Space Environ Med; 2007 Jun;78(6):627-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Venous angioma in an airman.
  • Cerebral venous angioma generally has a benign clinical course; however, it might cause cerebral hemorrhage or seizure.
  • On evaluation of an applicant with cerebral hemorrhage due to venous angioma, ruling out other primary diseases is important to consider about the potential of incapacitation.
  • [MeSH-major] Aerospace Medicine. Brain / abnormalities. Central Nervous System Venous Angioma / complications. Cerebral Hemorrhage / etiology

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  • (PMID = 17571667.001).
  • [ISSN] 0095-6562
  • [Journal-full-title] Aviation, space, and environmental medicine
  • [ISO-abbreviation] Aviat Space Environ Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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92. Kumar GS, Poonnoose SI, Chacko AG, Rajshekhar V: Trigonal cavernous angiomas: report of three cases and review of literature. Surg Neurol; 2006 Apr;65(4):367-71, discussion 371
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Trigonal cavernous angiomas: report of three cases and review of literature.
  • BACKGROUND: Intraventricular cavernous angiomas are very rare.
  • Only few cases of trigonal angiomas have been reported.
  • CASE DESCRIPTION: We report three cases of trigonal cavernous angiomas who presented with raised intracranial pressure or seizures and who underwent total excision with a good recovery.
  • CONCLUSION: On magnetic resonance imaging, intraventricular cavernous angiomas lack the hemosiderin ring characteristically seen around parenchymal cavernous angiomas.
  • This explains why trigonal cavernous angiomas can mimic malignant neoplasm on imaging, and they should be considered in the differential diagnosis of intraventricular masses.
  • [MeSH-major] Brain Neoplasms / diagnosis. Brain Neoplasms / surgery. Hemangioma, Cavernous, Central Nervous System / diagnosis. Hemangioma, Cavernous, Central Nervous System / surgery. Lateral Ventricles / pathology. Lateral Ventricles / surgery
  • [MeSH-minor] Adult. Arteriovenous Malformations / diagnosis. Child. Diagnosis, Differential. Diagnostic Errors / prevention & control. Female. Glioma / diagnosis. Headache / etiology. Headache / physiopathology. Hemianopsia / etiology. Hemianopsia / physiopathology. Humans. Intracranial Hypertension / etiology. Intracranial Hypertension / physiopathology. Magnetic Resonance Imaging. Male. Meningioma / diagnosis. Neurosurgical Procedures / methods. Paresis / etiology. Paresis / physiopathology. Seizures / etiology. Tomography, X-Ray Computed. Treatment Outcome

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  • (PMID = 16531197.001).
  • [ISSN] 0090-3019
  • [Journal-full-title] Surgical neurology
  • [ISO-abbreviation] Surg Neurol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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93. Nishikawa M, Ohata K, Ishibashi K, Takami T, Goto T, Hara M: The anterolateral partial vertebrectomy approach for ventrally located cervical intramedullary cavernous angiomas. Neurosurgery; 2006 Jul;59(1 Suppl 1):ONS58-63; discussion ONS58-63
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] The anterolateral partial vertebrectomy approach for ventrally located cervical intramedullary cavernous angiomas.
  • OBJECTIVE: We report three cases with ventral cervical intramedullary cavernous angiomas.
  • MATERIALS AND METHODS: All three patients presented with numbness in the upper extremities and investigation revealed a cavernous angioma on the ventral aspect of the spinal cord in each case.
  • RESULTS: Complete resection of the cavernous angioma was performed in all patients.
  • CONCLUSION: Anterolateral partial vertebrectomy provides direct exposure and is probably an ideal approach for selected cases with ventrally located intramedullary cavernous angiomas.
  • [MeSH-major] Cervical Vertebrae / surgery. Hemangioma, Cavernous, Central Nervous System / surgery. Neurosurgical Procedures / methods. Spinal Cord Neoplasms / surgery. Vascular Surgical Procedures / methods

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  • (PMID = 16888552.001).
  • [ISSN] 1524-4040
  • [Journal-full-title] Neurosurgery
  • [ISO-abbreviation] Neurosurgery
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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94. Kamiyama H, Nishimura S, Kaimori M, Watanabe M, Furuno Y, Saito A, Nishijima M: Cavernous angioma associated with arteriovenous malformation of the brain--case report. Neurol Med Chir (Tokyo); 2010;50(2):131-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cavernous angioma associated with arteriovenous malformation of the brain--case report.
  • A 61-year-old man presented a rare case of cerebral cavernous angioma associated with cerebral arteriovenous malformation (AVM) manifesting as headache.
  • Magnetic resonance imaging showed an AVM in the right occipital lobe and a cavernous angioma in the left middle fossa.
  • The histological diagnoses were cavernous angioma and AVM, respectively.
  • [MeSH-major] Brain Neoplasms / pathology. Hemangioma, Cavernous, Central Nervous System / pathology. Intracranial Arteriovenous Malformations / pathology. Sella Turcica / pathology. Skull Base Neoplasms / pathology

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  • (PMID = 20185878.001).
  • [ISSN] 1349-8029
  • [Journal-full-title] Neurologia medico-chirurgica
  • [ISO-abbreviation] Neurol. Med. Chir. (Tokyo)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Angiogenic Proteins; 0 / Biomarkers, Tumor
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95. Granel B, Serratrice J, de Roux-Serratrice C, Ene N, Disdier P, Weiller PJ: Multiple cutaneous angiomas and Poems syndrome. Presse Med; 2006 Mar;35(3 Pt 1):430-2
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  • [Title] Multiple cutaneous angiomas and Poems syndrome.
  • CASE: We describe here a case in which the eruption of diffuse cutaneous angiomas in a woman with a history of bone plasmocytoma and progressive polyneuropathy helped physicians to diagnose Poems syndrome.
  • [MeSH-major] Hemangioma / etiology. POEMS Syndrome / complications. Skin Neoplasms / etiology

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  • (PMID = 16550137.001).
  • [ISSN] 0755-4982
  • [Journal-full-title] Presse medicale (Paris, France : 1983)
  • [ISO-abbreviation] Presse Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Steroids
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96. Carrasco R, Pedrosa M, Pascual JM, Navas M, Liberal R, Sola RG: Cavernous angiomas of the lateral ventricles. Acta Neurochir (Wien); 2009 Feb;151(2):149-54

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cavernous angiomas of the lateral ventricles.
  • BACKGROUND: Cavernous angiomas are vascular malformations which rarely involve the cavities of the lateral ventricles.
  • [MeSH-major] Cerebral Ventricle Neoplasms / pathology. Hemangioma, Cavernous, Central Nervous System / pathology. Lateral Ventricles / pathology

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  • (PMID = 19194650.001).
  • [ISSN] 0942-0940
  • [Journal-full-title] Acta neurochirurgica
  • [ISO-abbreviation] Acta Neurochir (Wien)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Austria
  • [Number-of-references] 42
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97. Sandhu K, Gupta S: Angioma serpiginosum: report of two unusual cases. J Eur Acad Dermatol Venereol; 2005 Jan;19(1):127-8
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  • [Title] Angioma serpiginosum: report of two unusual cases.
  • Angioma serpiginosum (AS) is a rare vascular naevoid disorder due to ectatic dilation of capillaries in the papillary dermis.
  • [MeSH-major] Skin Diseases, Vascular / diagnosis. Telangiectasis / diagnosis
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Humans. Leg. Thorax

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  • (PMID = 15649209.001).
  • [ISSN] 0926-9959
  • [Journal-full-title] Journal of the European Academy of Dermatology and Venereology : JEADV
  • [ISO-abbreviation] J Eur Acad Dermatol Venereol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
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98. Blansfield JA, Goldhahn RT Jr, Josloff RK: Littoral cell angioma of the spleen treated by laparoscopic splenectomy. JSLS; 2005 Apr-Jun;9(2):222-4
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  • [Title] Littoral cell angioma of the spleen treated by laparoscopic splenectomy.
  • Massive splenomegaly due to multifocal littoral cell angioma was discovered incidentally in a 55-year-old man during a workup for an unrelated condition.
  • We report the second case of littoral cell angioma of the spleen treated laparoscopically.

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  • [Cites] AJR Am J Roentgenol. 2000 Feb;174(2):467-9 [10658726.001]
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  • (PMID = 15984716.001).
  • [ISSN] 1086-8089
  • [Journal-full-title] JSLS : Journal of the Society of Laparoendoscopic Surgeons
  • [ISO-abbreviation] JSLS
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC3015579
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99. Lim SC, Hong R, Kim YS, Jang SJ: Large cystic cavernous angioma of the cerebellum mimicking pilocytic astrocytoma. J Neurooncol; 2006 Sep;79(2):169-70
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Large cystic cavernous angioma of the cerebellum mimicking pilocytic astrocytoma.
  • OBJECTIVE AND IMPORTANCE: Cavernous angiomas are relatively rare vascular malformations.
  • Cavernous angiomas, accompanied by a large cyst, are very rare.
  • We present a case of a cavernous angioma with the unusual MRI findings of a large cyst and a small mural nodule.
  • CLINICAL PRESENTATION: The patient was a 48-year-old man who complained of a history of dizziness for several weeks.
  • Therefore, a rare cystic angioma must be considered in the differential diagnosis of infratentorial cystic masses.
  • [MeSH-major] Astrocytoma / diagnosis. Brain Neoplasms / diagnosis. Central Nervous System Cysts / diagnosis. Cerebellum / pathology. Hemangioma, Cavernous, Central Nervous System / diagnosis
  • [MeSH-minor] Diagnosis, Differential. Dizziness / etiology. Humans. Magnetic Resonance Imaging. Male. Middle Aged. Treatment Outcome

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  • (PMID = 16821089.001).
  • [ISSN] 0167-594X
  • [Journal-full-title] Journal of neuro-oncology
  • [ISO-abbreviation] J. Neurooncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
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100. Samii M, Nakamura M, Mirzai S, Vorkapic P, Cervio A: Cavernous angiomas within the internal auditory canal. J Neurosurg; 2006 Oct;105(4):581-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cavernous angiomas within the internal auditory canal.
  • OBJECT: The aim of this study was to describe the symptomatology, radiological features, and surgical treatment of patients with cavernous angiomas within the internal auditory canal (IAC).
  • METHODS: The authors reviewed the cases of seven patients with cavernous angiomas in the IAC that had been surgically treated in the 22-year period between 1983 and 2005.
  • Interestingly, these same angiomas showed variable features on magnetic resonance (MR) imaging, making their differentiation from intrameatal vestibular schwannomas (VSs) sometimes impossible.
  • CONCLUSIONS: Cavernous angiomas of the IAC are very uncommon lesions that can imitate the symptoms of VSs.
  • Thus, the preoperative diagnosis must be based on patient symptoms plus the CT and MR imaging features.
  • [MeSH-major] Ear Neoplasms / surgery. Hemangioma, Cavernous, Central Nervous System / surgery. Labyrinth Diseases / surgery
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Hearing Loss, Sensorineural / etiology. Humans. Magnetic Resonance Imaging. Male. Middle Aged. Postoperative Complications / etiology. Retrospective Studies. Tinnitus / etiology. Tomography, X-Ray Computed

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  • (PMID = 17044562.001).
  • [ISSN] 0022-3085
  • [Journal-full-title] Journal of neurosurgery
  • [ISO-abbreviation] J. Neurosurg.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 47
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