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1. Tripathy LN, Singh SN: Multiple giant cavernous angiomas of the brain. Neurol India; 2009 May-Jun;57(3):350-1

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple giant cavernous angiomas of the brain.
  • [MeSH-major] Central Nervous System Neoplasms / diagnosis. Hemangioma, Cavernous, Central Nervous System / diagnosis

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  • (PMID = 19587484.001).
  • [ISSN] 0028-3886
  • [Journal-full-title] Neurology India
  • [ISO-abbreviation] Neurol India
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] India
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2. Chen G, Leng B, Song D, Wang Q: Coexistence multiple intracerebral, spinal cavernous angiomas and multiple intracerebral meningiomas. Neurol India; 2010 Mar-Apr;58(2):332-3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Coexistence multiple intracerebral, spinal cavernous angiomas and multiple intracerebral meningiomas.
  • [MeSH-major] Hemangioma, Cavernous / complications. Meningeal Neoplasms / complications. Meningioma / complications

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  • (PMID = 20508370.001).
  • [ISSN] 0028-3886
  • [Journal-full-title] Neurology India
  • [ISO-abbreviation] Neurol India
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
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3. Detry O, De Roover A: Images in clinical medicine. Spider angiomas. N Engl J Med; 2009 Jan 15;360(3):280
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Images in clinical medicine. Spider angiomas.

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  • (PMID = 19144943.001).
  • [ISSN] 1533-4406
  • [Journal-full-title] The New England journal of medicine
  • [ISO-abbreviation] N. Engl. J. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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4. Mathews MS, Peck WW, Brant-Zawadzki M: Brown-Séquard syndrome secondary to spontaneous bleed from postradiation cavernous angiomas. AJNR Am J Neuroradiol; 2008 Nov;29(10):1989-90
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  • [Title] Brown-Séquard syndrome secondary to spontaneous bleed from postradiation cavernous angiomas.
  • We report a rare case of Brown-Séquard syndrome from spontaneous intraspinal hemorrhage in a patient with multiple cavernous angiomas in the spinal cord secondary to craniospinal radiation in childhood.
  • [MeSH-major] Brown-Sequard Syndrome / diagnosis. Brown-Sequard Syndrome / etiology. Cerebral Hemorrhage / diagnosis. Cerebral Hemorrhage / etiology. Hemangioma, Cavernous / complications. Neoplasms, Radiation-Induced / complications. Radiotherapy / adverse effects

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  • (PMID = 18617590.001).
  • [ISSN] 1936-959X
  • [Journal-full-title] AJNR. American journal of neuroradiology
  • [ISO-abbreviation] AJNR Am J Neuroradiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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5. Calvo Hernández R, Erdozain Sosa JC, Segura Cabral JM: [Unusual complication of spider angiomas: hemorrhagic diathesis controlled with antihormonal therapy (tamoxifen)]. Rev Esp Enferm Dig; 2006 Jul;98(7):558-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Unusual complication of spider angiomas: hemorrhagic diathesis controlled with antihormonal therapy (tamoxifen)].
  • [Transliterated title] Complicacion inusual de las arañas vasculares: diátesis hemorrágica con control del sangrado con terapia antihormonal (tamoxifeno).
  • [MeSH-major] Hemangioma / therapy. Skin Neoplasms / therapy
  • [MeSH-minor] Antineoplastic Agents, Hormonal / therapeutic use. Cautery. Female. Hemorrhage / etiology. Hepatopulmonary Syndrome / diagnosis. Humans. Middle Aged. Tamoxifen / therapeutic use

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  • (PMID = 17022709.001).
  • [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] Case Reports; Letter
  • [Publication-country] Spain
  • [Chemical-registry-number] 0 / Antineoplastic Agents, Hormonal; 094ZI81Y45 / Tamoxifen
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6. Huo L, Wu L, Zhang MY, Hou YH, Ding XP, Fang JS: [Electrocorticography monitoring in microsurgical treatment of solitary cavernous angiomas]. Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2008 May;33(5):448-51

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Electrocorticography monitoring in microsurgical treatment of solitary cavernous angiomas].
  • OBJECTIVE: To investigate the curative effect of electrocorticography (ECoG) monitoring in the microsurgical treatment of cavernous angiomas.
  • METHODS: Clinical data of 71 patients with epileptogenic cavernous angiomas,who had been performed ECoG monitoring during the operation,were analyzed retrospectively.
  • RESULTS: The foci of cavernous angiomas and epilepsy of the 71 patients were resected during the operation.
  • CONCLUSION: The drug treatment of epileptogenic cavernous angiomas can not control epileptic seizure,and the patients should receive the microsurgical treatment early.
  • [MeSH-major] Cerebral Cortex / physiopathology. Electroencephalography. Hemangioma, Cavernous, Central Nervous System / surgery. Microsurgery / methods. Monitoring, Intraoperative / methods

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  • (PMID = 18544851.001).
  • [ISSN] 1672-7347
  • [Journal-full-title] Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences
  • [ISO-abbreviation] Zhong Nan Da Xue Xue Bao Yi Xue Ban
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
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7. Alves de Sousa A: [Deep-seated (corpus callosum, intraventricular, basal ganglia and insula) and brain stem cavernous angiomas. Experience in Brazil]. Neurochirurgie; 2007 Jun;53(2-3 Pt 2):182-91

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Deep-seated (corpus callosum, intraventricular, basal ganglia and insula) and brain stem cavernous angiomas. Experience in Brazil].
  • [Transliterated title] Cavernomes profonds (corps calleux, intraventriculaires, ganglions de la base, insulaires) et du tronc cérébral. Expérience d'une série brésilienne.
  • [MeSH-major] Basal Ganglia / pathology. Brain Stem / pathology. Central Nervous System Neoplasms / pathology. Cerebral Cortex / pathology. Cerebral Ventricles / pathology. Corpus Callosum / pathology. Hemangioma, Cavernous, Central Nervous System / pathology

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  • (PMID = 17507054.001).
  • [ISSN] 0028-3770
  • [Journal-full-title] Neuro-Chirurgie
  • [ISO-abbreviation] Neurochirurgie
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] France
  • [Number-of-references] 44
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8. Miyazawa A, Inoue M, Hirakata A, Okada AA, Iihara K, Fujioka Y: Expression of inhibin alpha by stromal cells of retinal angiomas excised from a patient with von Hippel-Lindau disease. Jpn J Ophthalmol; 2009 Sep;53(5):501-5
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  • [Title] Expression of inhibin alpha by stromal cells of retinal angiomas excised from a patient with von Hippel-Lindau disease.
  • BACKGROUND: To report the results of immunohistochemical analyses of a retinal angioma obtained from a patient with von Hippel-Lindau (VHL) disease.
  • CASE: A 13-year-old girl with VHL disease presented with bilateral retinal angiomas and decreased vision in the right eye.
  • Although transpupillary thermotherapy was performed to treat the angiomas, the tractional and exudative retinal detachment progressed OD, requiring vitreous surgery.
  • Intraoperatively, a large retinal angioma was excised together with the surrounding retina to aid in reattaching the retina.
  • These findings are identical to those of a hemangioblastoma.
  • CONCLUSIONS: The results indicate that stromal cells in retinal angiomas are neuroectodermal in origin with immunohistochemical features, for example, inhibin alpha, similar to cerebellar hemangioblastomas and renal cell carcinomas associated with VHL disease.
  • [MeSH-major] Hemangioma / metabolism. Inhibins / metabolism. Retinal Neoplasms / metabolism. von Hippel-Lindau Disease / metabolism

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  • (PMID = 19847606.001).
  • [ISSN] 1613-2246
  • [Journal-full-title] Japanese journal of ophthalmology
  • [ISO-abbreviation] Jpn. J. Ophthalmol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Glial Fibrillary Acidic Protein; 0 / VEGFA protein, human; 0 / Vascular Endothelial Growth Factor A; 0 / inhibin-alpha subunit; 11096-26-7 / Erythropoietin; 57285-09-3 / Inhibins; EC 4.2.1.11 / Phosphopyruvate Hydratase
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9. Beall DP, Bell JP, Webb JR, Fish JR: Developmental venous anomalies and cavernous angiomas: a review of the concurrence, imaging, and treatment of these vascular malformations. J Okla State Med Assoc; 2005 Nov;98(11):535-8
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  • [Title] Developmental venous anomalies and cavernous angiomas: a review of the concurrence, imaging, and treatment of these vascular malformations.
  • Deep venous anomalies and cavernous angiomas are two distinct intracranial lesions.
  • Several imaging modalities can be used to evaluate these distinct lesions and often more than one are needed for a prompt and reliable diagnosis.
  • [MeSH-major] Brain Neoplasms. Hemangioma
  • [MeSH-minor] Hemangioma, Cavernous / diagnosis. Hemangioma, Cavernous / surgery. Humans

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  • (PMID = 16379482.001).
  • [ISSN] 0030-1876
  • [Journal-full-title] The Journal of the Oklahoma State Medical Association
  • [ISO-abbreviation] J Okla State Med Assoc
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 13
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10. Sessa A, Battini G, Meroni M, Pitingolo F, Righetti M, Ciotti P, Di Maria E, Bellone E, Ajmar F, Mandich P: Multifocal bilateral renal cell carcinoma and retinal angiomas in a patient with de novo von Hippel-Lindau disease: identification of a new germline mutation. J Nephrol; 2005 Mar-Apr;18(2):209-12
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  • [Title] Multifocal bilateral renal cell carcinoma and retinal angiomas in a patient with de novo von Hippel-Lindau disease: identification of a new germline mutation.
  • Von Hippel-Lindau (VHL) disease is a rare autosomal dominant disorder characterized by multifocal and bilateral renal cell carcinoma and cysts, retinal angiomas, hemangioblastoma of the central nervous system, pheochromocytoma, epididymis cystoadenoma, pancreatic cysts and/or islet cell tumors.
  • It is well known that about 25% of VHL patients present de novo mutations, and first cases function as possible founders of new VHL kindreds.
  • Herein, we report the clinical case of a 45-year-old Caucasian female patient affected by bilateral polycystic kidney disease with two renal carcinomas in both kidneys without lynphoadenopathies.
  • The genetic study of the unaffected parents and of the unaffected brother confirmed the diagnosis of de novo VHL disease with the dentification of a new germline mutation, never reported in the literature.
  • The patient showed normal kidney function and she did not show other organ lesions or clinical manifestations of VHL disease.
  • [MeSH-major] Carcinoma, Renal Cell / genetics. Germ-Line Mutation. Hemangioma / genetics. Kidney Neoplasms / genetics. Retinal Neoplasms / genetics. von Hippel-Lindau Disease / genetics
  • [MeSH-minor] Female. Humans. Middle Aged. Polycystic Kidney Diseases / genetics


11. 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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12. 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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  • [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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13. 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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14. Matin SF, McCutcheon IE, Gombos DS, Waguespack SG, Wen S, Smith LA, Zhang Y, Davis DW, Fuller G, Jonasch E: Treatment of VHL patients with sunitinib: Clinical observations and translational studies. J Clin Oncol; 2009 May 20;27(15_suppl):e22047

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • : e22047 Background: Von Hippel Lindau (VHL) disease induces vascular lesions in multiple organs.
  • Eligibility criteria included retinal angiomas, hemangioblastomas (HBs) measuring at least 5mm, renal cell carcinoma (RCC) 1 to 3 cm and pancreatic neuroendocrine tumors (NETs) 1 to 3 cm.

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  • (PMID = 27963229.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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15. Noto S, Fujii M, Akimura T, Imoto H, Nomura S, Kajiwara K, Kato S, Fujisawa H, Suzuki M: Management of patients with cavernous angiomas presenting epileptic seizures. Surg Neurol; 2005 Dec;64(6):495-8, discussion 498-9
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  • [Title] Management of patients with cavernous angiomas presenting epileptic seizures.
  • BACKGROUND: The aim of this study was to establish a treatment strategy for patients with cavernous angiomas and have seizures.
  • METHODS: We analyzed retrospectively 31 patients with cavernous angiomas presenting with seizures.
  • CONCLUSIONS: Surgical intervention may have greater benefits than medical intervention for patients with cavernous angiomas presenting with epileptic seizures.
  • [MeSH-major] Hemangioma, Cavernous / complications. Hemangioma, Cavernous / surgery. Seizures / etiology

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  • (PMID = 16293460.001).
  • [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 / Anticonvulsants
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16. 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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17. 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

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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18. Marasco R, Spagnoli M, Leonardi M: Association between Developmental Venous Anomalies and Cavernous Angiomas: a Retrospective MR Study. Neuroradiol J; 2009 May 15;22(2):179-85

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Association between Developmental Venous Anomalies and Cavernous Angiomas: a Retrospective MR Study.
  • Many studies suggested and then confirmed the association between cavernous angioma and developmental venous anomaly, described for the first time by Roberson in 1974.

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  • (PMID = 24207037.001).
  • [ISSN] 1971-4009
  • [Journal-full-title] The neuroradiology journal
  • [ISO-abbreviation] Neuroradiol J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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19. 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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20. Kobayashi E, Bagshaw AP, Gotman J, Dubeau F: Metabolic correlates of epileptic spikes in cerebral cavernous angiomas. Epilepsy Res; 2007 Jan;73(1):98-103
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Metabolic correlates of epileptic spikes in cerebral cavernous angiomas.
  • BACKGROUND: Cerebral cavernous angiomas (CCA) are frequently associated with focal intractable epilepsy.
  • We also demonstrated diffuse rather than focal responses, in accordance with previous studies in lesional and non-lesional temporal lobe epilepsy, confirming the frequent distant effect of epileptic spikes.
  • [MeSH-major] Brain Neoplasms / physiopathology. Epilepsy, Temporal Lobe / etiology. Hemangioma, Cavernous / physiopathology. Seizures / physiopathology

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  • (PMID = 17000081.001).
  • [ISSN] 0920-1211
  • [Journal-full-title] Epilepsy research
  • [ISO-abbreviation] Epilepsy Res.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Netherlands
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21. Shalek PA, Vinogradov BM, Pozdniakov AV, Stukov LA, Garmashov IuA: [Methods and results of stereotactic radiosurgery for cavernous angiomas]. Vopr Onkol; 2008;54(4):525-8
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  • [Title] [Methods and results of stereotactic radiosurgery for cavernous angiomas].
  • They presented with 47 cavernous angiomas and 44 of them underwent surgery.
  • [MeSH-major] Brain Neoplasms / surgery. Hemangioma, Cavernous / surgery. Radiosurgery

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  • (PMID = 18942415.001).
  • [ISSN] 0507-3758
  • [Journal-full-title] Voprosy onkologii
  • [ISO-abbreviation] Vopr Onkol
  • [Language] rus
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Russia (Federation)
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22. 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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  • [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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23. 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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  • [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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24. 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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  • [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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25. 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

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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26. Gao XH, Wang LL, Zhang L, Hong YX, Wei H, Chen HD: Familial nevus flammeus associated with early onset cherry angiomas. Int J Dermatol; 2008 Dec;47(12):1284-6
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  • [Title] Familial nevus flammeus associated with early onset cherry angiomas.
  • [MeSH-major] Hemangioma / genetics. Port-Wine Stain / genetics. Skin Neoplasms / genetics

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  • (PMID = 19126018.001).
  • [ISSN] 1365-4632
  • [Journal-full-title] International journal of dermatology
  • [ISO-abbreviation] Int. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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27. Maronn M, Chamlin S, Metry D: Multifocal tufted angiomas in 2 infants. Arch Dermatol; 2009 Jul;145(7):847-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multifocal tufted angiomas in 2 infants.
  • [MeSH-major] Hemangioma / pathology. Skin Neoplasms / pathology

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  • (PMID = 19620578.001).
  • [ISSN] 1538-3652
  • [Journal-full-title] Archives of dermatology
  • [ISO-abbreviation] Arch Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] United States
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28. Awad IA: From mutant mice to "vascular permeability therapy" in cavernous angiomas? Neurosurgery; 2009 May;64(5):N10
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] From mutant mice to "vascular permeability therapy" in cavernous angiomas?
  • [MeSH-major] Brain Neoplasms. Hemangioma, Cavernous
  • [MeSH-minor] Animals. Carrier Proteins / genetics. Disease Models, Animal. Humans. Mice. Mice, Mutant Strains

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  • (PMID = 19404130.001).
  • [ISSN] 1524-4040
  • [Journal-full-title] Neurosurgery
  • [ISO-abbreviation] Neurosurgery
  • [Language] eng
  • [Publication-type] Editorial
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / CCM2 protein, human; 0 / Carrier Proteins
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29. Soo JK, Mortimer PS: Eruptive angiomas associated with graft-versus-host disease. Br J Dermatol; 2006 Feb;154(2):376-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Eruptive angiomas associated with graft-versus-host disease.
  • [MeSH-major] Graft vs Host Disease / complications. Hemangioma / etiology. Skin Neoplasms / etiology

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  • (PMID = 16433816.001).
  • [ISSN] 0007-0963
  • [Journal-full-title] The British journal of dermatology
  • [ISO-abbreviation] Br. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] England
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30. 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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31. Kuwahara H, Noguchi Y, Saito Y, Inaba A: Multiple cavernous angiomas in the brain and spinal cord. Arch Neurol; 2010 Nov;67(11):1405-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple cavernous angiomas in the brain and spinal cord.
  • [MeSH-major] Brain / pathology. Hemangioma, Cavernous, Central Nervous System / pathology. Seizures / pathology. Spinal Cord / pathology

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  • (PMID = 21060020.001).
  • [ISSN] 1538-3687
  • [Journal-full-title] Archives of neurology
  • [ISO-abbreviation] Arch. Neurol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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32. [Angiomas]. Ann Dermatol Venereol; 2005 Oct;132(10 Suppl):7S172-7S177
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  • [Title] [Angiomas].
  • [MeSH-major] Arteriovenous Malformations / diagnosis. Arteriovenous Malformations / pathology. Hemangioma / diagnosis. Hemangioma / pathology
  • [MeSH-minor] Diagnosis, Differential. Humans

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  • (PMID = 16419542.001).
  • [ISSN] 0151-9638
  • [Journal-full-title] Annales de dermatologie et de vénéréologie
  • [ISO-abbreviation] Ann Dermatol Venereol
  • [Language] fre
  • [Publication-type] Journal Article
  • [Publication-country] France
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33. Enjolras O: [Angiomas and angiomatosis]. Presse Med; 2010 Apr;39(4):454-6
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  • [Title] [Angiomas and angiomatosis].
  • [MeSH-major] Angiomatosis / physiopathology. Hemangioma / physiopathology
  • [MeSH-minor] Child. Congresses as Topic. Humans. International Cooperation. Societies, Medical. Terminology as Topic. Vascular Malformations / physiopathology

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  • (PMID = 20207517.001).
  • [ISSN] 2213-0276
  • [Journal-full-title] Presse medicale (Paris, France : 1983)
  • [ISO-abbreviation] Presse Med
  • [Language] fre
  • [Publication-type] Editorial
  • [Publication-country] France
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34. Maciunas JA, Syed TU, Cohen ML, Werz MA, Maciunas RJ, Koubeissi MZ: Triple pathology in epilepsy: coexistence of cavernous angiomas and cortical dysplasias with other lesions. Epilepsy Res; 2010 Sep;91(1):106-10
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Triple pathology in epilepsy: coexistence of cavernous angiomas and cortical dysplasias with other lesions.
  • In addition, each of these patients had a third form of a potentially epileptogenic lesion: hippocampal sclerosis in one, and venous angioma in the other.
  • [MeSH-major] Brain Neoplasms / pathology. Epilepsy / pathology. Hemangioma, Cavernous / pathology. Malformations of Cortical Development / pathology

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  • [Copyright] Copyright 2010 Elsevier B.V. All rights reserved.
  • (PMID = 20674276.001).
  • [ISSN] 1872-6844
  • [Journal-full-title] Epilepsy research
  • [ISO-abbreviation] Epilepsy Res.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
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35. Naouri M, Lorette G: [Angiomas]. Rev Prat; 2009 Dec 20;59(10):1450
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Angiomas].
  • [MeSH-major] Hemangioma / therapy. Skin Neoplasms / therapy

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  • (PMID = 20058768.001).
  • [ISSN] 0035-2640
  • [Journal-full-title] La Revue du praticien
  • [ISO-abbreviation] Rev Prat
  • [Language] fre
  • [Publication-type] Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Adrenergic beta-Antagonists; 9Y8NXQ24VQ / Propranolol
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36. Naouri M, Lorette G: [Angiomas]. Rev Prat; 2006 Oct 31;56(16):1835-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Angiomas].
  • [MeSH-major] Hemangioma / diagnosis
  • [MeSH-minor] Age Factors. Angiodysplasia / diagnosis. Arm. Arteriovenous Malformations / diagnosis. Diagnosis, Differential. Eyelid Neoplasms / diagnosis. Facial Neoplasms / diagnosis. Female. Humans. Infant. Infant, Newborn. Lip Neoplasms / diagnosis. Lymphangioma / diagnosis. Magnetic Resonance Imaging. Male. Neoplasm Regression, Spontaneous. Prognosis. Sturge-Weber Syndrome / diagnosis. Telangiectasis / diagnosis. Time Factors. Ultrasonography, Doppler. Veins / abnormalities

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  • (PMID = 17315512.001).
  • [ISSN] 0035-2640
  • [Journal-full-title] La Revue du praticien
  • [ISO-abbreviation] Rev Prat
  • [Language] fre
  • [Publication-type] Journal Article; Review
  • [Publication-country] France
  • [Number-of-references] 0
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37. Ma HJ, Zhao G, Shi F, Wang YX: Eruptive cherry angiomas associated with vitiligo: provoked by topical nitrogen mustard? J Dermatol; 2006 Dec;33(12):877-9
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  • [Title] Eruptive cherry angiomas associated with vitiligo: provoked by topical nitrogen mustard?
  • We report a 27-year-old man who had suffered with vitiligo for 7 years and with eruptive cherry angiomas within or around the repigmented vitiliginous skin for 2 years.
  • After continual therapy for vitiligo with topical nitrogen mustard in a concentration of 0.001% for 5 years, multiple cherry angiomas erupted within or around the repigmented vitiliginous plaques.
  • The discontinue therapy with nitrogen mustard stopped the appearance of new cherry angiomas.
  • The presence of eruptive cherry angiomas was evident and was confirmed by histopathology.
  • We suggest that the chronic chemical stimuli caused by topical nitrogen mustard might result in the formation of eruptive cherry angiomas.
  • [MeSH-major] Alkylating Agents / adverse effects. Dermatologic Agents / adverse effects. Hemangioma / chemically induced. Mechlorethamine / adverse effects. Skin Neoplasms / chemically induced. Vitiligo / drug therapy


38. Cantu C, Murillo-Bonilla L, Arauz A, Higuera J, Padilla J, Barinagarrementeria F: Predictive factors for intracerebral hemorrhage in patients with cavernous angiomas. Neurol Res; 2005 Apr;27(3):314-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Predictive factors for intracerebral hemorrhage in patients with cavernous angiomas.
  • OBJECTIVES: Prediction of intracerebral hemorrhage (ICH) in patients with cavernous angiomas is not totally elucidated.
  • The aims of our study were to determine the rate of cerebral hemorrhage, its associated factors, and the clinical outcome in patients with cavernous angiomas in a Hispanic population.
  • METHODS: We studied 133 patients with cavernous angiomas.
  • Non-lobar location of angiomas was associated with hemorrhage [OR 4.82 (CI 95% 2.17-10.73; p=<0.001)].
  • In contrast, factors associated with a decreased risk of hemorrhage were a family history of epilepsy [OR 0.30 (CI 95% 0.10-0.79; p=0.016)] and lobar location of the angiomas [OR 0.21 (CI 95% 0.09-0.46; p=<0.001)].
  • It was only 1.22% per patient per year in lobar angiomas and 2.33, 2.39, and 2.82% per patient per year for brainstem, cerebellum, and deep hemispheric angiomas, respectively.
  • CONCLUSIONS: The non-lobar location of cavernous angiomas gives a higher risk of hemorrhage in our Mexican mestizo population, without the hemorrhage being related to either age or sex.
  • [MeSH-major] Cerebral Hemorrhage / epidemiology. Cerebral Hemorrhage / etiology. Hemangioma, Cavernous / complications. Risk

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  • (PMID = 15845215.001).
  • [ISSN] 0161-6412
  • [Journal-full-title] Neurological research
  • [ISO-abbreviation] Neurol. Res.
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] England
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39. 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

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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40. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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41. Bernotas G, Rastenyte D, Deltuva V, Matukevicius A, Jaskeviciene V, Tamasauskas A: Cavernous angiomas: an uncontrolled clinical study of 87 surgically treated patients. Medicina (Kaunas); 2009;45(1):21-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cavernous angiomas: an uncontrolled clinical study of 87 surgically treated patients.
  • BACKGROUND: Cerebral cavernous angiomas remain as one of the most negotiable and controversial topics in neurological and neurosurgical practice.
  • We present statistical evaluation of initial presentation, preoperative neurological findings, surgical complications, and outcome of surgically treated patients with intracerebral cavernous angiomas.
  • METHODS: During 1997 to 2004, 87 patients (41 men, 46 women) with intracerebral cavernous angiomas underwent surgical treatment in the tertiary referral center, and these were included into the present uncontrolled clinical study.
  • A simplified version of Engel's classification of the outcome of the patients with chronic seizures was applied.
  • RESULTS: The most common clinical presentation of cavernous angiomas was seizures, significant part of which was chronic.
  • CONCLUSIONS: Microsurgical removal of cavernous angiomas and surrounding hemosiderin plate tends to significant reduction or elimination of epileptic seizures and improved postoperative neurological status.
  • [MeSH-major] Brain Neoplasms / surgery. Hemangioma, Cavernous / surgery. Neoplasms, Multiple Primary / surgery
  • [MeSH-minor] Adolescent. Adult. Aged. Cerebral Hemorrhage / etiology. Chi-Square Distribution. Child. Chronic Disease. Data Interpretation, Statistical. Electrocardiography. Epilepsy / etiology. Female. Headache / etiology. Humans. Karnofsky Performance Status. Magnetic Resonance Imaging. Male. Microsurgery. Middle Aged. Seizures / etiology. Statistics, Nonparametric. Treatment Outcome

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  • (PMID = 19223702.001).
  • [ISSN] 1648-9144
  • [Journal-full-title] Medicina (Kaunas, Lithuania)
  • [ISO-abbreviation] Medicina (Kaunas)
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] Lithuania
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42. Caruso G, Galarza M, Borghesi I, Pozzati E, Vitale M: Acute presentation of spinal epidural cavernous angiomas: case report. Neurosurgery; 2007 Mar;60(3):E575-6; discussion E576

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Acute presentation of spinal epidural cavernous angiomas: case report.
  • OBJECTIVE: Spinal extramedullary hematomas stemming from cavernous angiomas in the epidural compartment are rare.
  • It is more common for spinal epidural cavernous angiomas to present with slow and progressive myelopathy or radiculopathy.
  • CLINICAL PRESENTATION: Three consecutive cases of acute spinal cavernous angiomas with overt neurological deficits were presented.
  • CONCLUSION: Spontaneous spinal epidural hematomas presented with significant pain and acute spinal cord and nerve root compression may represent the manifestation of a cavernous angioma.
  • [MeSH-major] Epidural Neoplasms / diagnosis. Epidural Neoplasms / surgery. Hemangioma, Cavernous / diagnosis. Hemangioma, Cavernous / surgery
  • [MeSH-minor] Acute Disease. Adult. Aged. Critical Care / methods. Humans. Laminectomy. Lumbar Vertebrae. Male. Treatment Outcome

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  • (PMID = 17327768.001).
  • [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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43. Dahl ME, Bothwell M, Hirschi SD: Multiple angiomas of the external auditory canal in a patient with Sturge-Weber syndrome. Ear Nose Throat J; 2007 Jan;86(1):15
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple angiomas of the external auditory canal in a patient with Sturge-Weber syndrome.

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  • (PMID = 17315824.001).
  • [ISSN] 0145-5613
  • [Journal-full-title] Ear, nose, & throat journal
  • [ISO-abbreviation] Ear Nose Throat J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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44. Labauge P, Denier C, Bergametti F, Tournier-Lasserve E: Genetics of cavernous angiomas. Lancet Neurol; 2007 Mar;6(3):237-44

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Genetics of cavernous angiomas.
  • Cerebral cavernous malformations (CCM) are vascular malformations that can occur as a sporadic or a familial autosomal dominant disorder.
  • Clinical and cerebral MRI data on large series of patients with a genetic form of the disease are now available.
  • These recent developments in clinical and molecular genetics have given us useful information about clinical care and genetic counselling and have broadened our understanding of the mechanisms of this disorder.
  • [MeSH-major] Hemangioma, Cavernous / genetics

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  • (PMID = 17303530.001).
  • [ISSN] 1474-4422
  • [Journal-full-title] The Lancet. Neurology
  • [ISO-abbreviation] Lancet Neurol
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] England
  • [Number-of-references] 84
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45. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • 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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46. Tirakotai W, Sure U, Benes L, Krischek B, Bien S, Bertalanffy H: Image-guided transsylvian, transinsular approach for insular cavernous angiomas. Neurosurgery; 2007 Jul;61(1 Suppl):423-30; discussion 430-1

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Image-guided transsylvian, transinsular approach for insular cavernous angiomas.
  • METHODS: Between 1997 and 2003, with the guidance of a frameless stereotactic system (BrainLab AG, Munich, Germany), we operated on eight patients who harbored an insular cavernoma.
  • Neuronavigation was used for 1) accurate planning of the craniotomy, 2) identification of the distal sylvian fissure, and, finally, 3) finding the exact site for insular corticotomy.
  • Accordingly, safe exposure can be obtained because of a tailored dissection of the sylvian fissure and minimal insular corticotomy.

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  • [ReprintOf] Neurosurgery. 2003 Dec;53(6):1299-304; discussion 1304-5 [14633296.001]
  • (PMID = 18813148.001).
  • [ISSN] 1524-4040
  • [Journal-full-title] Neurosurgery
  • [ISO-abbreviation] Neurosurgery
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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47. Zahedi S, Yang C, O'Hanlon D, Tanev K, Shea WP: Electroconvulsive therapy and venous angiomas: two case reports and review of the literature. J ECT; 2006 Sep;22(3):228-30

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Electroconvulsive therapy and venous angiomas: two case reports and review of the literature.
  • However, there is a paucity of cases presenting ECT in the context of a cerebral venous angioma.
  • In this article, we present 2 cases of patients treated with ECT who were found to have documented venous angiomas.
  • [MeSH-major] Central Nervous System Venous Angioma / complications. Electroconvulsive Therapy
  • [MeSH-minor] Adult. Aged. Bipolar Disorder / complications. Bipolar Disorder / pathology. Bipolar Disorder / therapy. Depressive Disorder, Major / complications. Depressive Disorder, Major / pathology. Depressive Disorder, Major / therapy. Female. Humans. Male. Stress Disorders, Post-Traumatic / complications. Stress Disorders, Post-Traumatic / pathology. Stress Disorders, Post-Traumatic / therapy

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  • (PMID = 16957543.001).
  • [ISSN] 1095-0680
  • [Journal-full-title] The journal of ECT
  • [ISO-abbreviation] J ECT
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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48. Miyake S, Uchihashi Y, Takaishi Y, Sakagami Y, Kohmura E: Multiple cavernous angiomas of the cauda equina. Case report. Neurol Med Chir (Tokyo); 2007 Apr;47(4):178-81

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple cavernous angiomas of the cauda equina. Case report.
  • An 18-year-old male presented with multiple cavernous angiomas of the cauda equina manifesting as acute onset of severe low back pain radiating into the bilateral legs.
  • Histological examination revealed cavernous angioma.
  • [MeSH-major] Cauda Equina. Hemangioma, Cavernous / diagnosis. Peripheral Nervous System Neoplasms / diagnosis

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  • (PMID = 17457023.001).
  • [ISSN] 0470-8105
  • [Journal-full-title] Neurologia medico-chirurgica
  • [ISO-abbreviation] Neurol. Med. Chir. (Tokyo)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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49. Yeon JY, Kim JS, Choi SJ, Seo DW, Hong SB, Hong SC: Supratentorial cavernous angiomas presenting with seizures: surgical outcomes in 60 consecutive patients. Seizure; 2009 Jan;18(1):14-20
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Supratentorial cavernous angiomas presenting with seizures: surgical outcomes in 60 consecutive patients.
  • The aim of this study is to determine surgical outcomes and factors affecting seizure outcomes in patients who harbor supratentorial cavernous angiomas presenting with seizures.
  • [MeSH-major] Hemangioma, Cavernous, Central Nervous System / surgery. Psychosurgery / methods. Seizures / surgery. Supratentorial Neoplasms / surgery

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  • (PMID = 18656386.001).
  • [ISSN] 1059-1311
  • [Journal-full-title] Seizure
  • [ISO-abbreviation] Seizure
  • [Language] eng
  • [Publication-type] Clinical Trial; Journal Article
  • [Publication-country] England
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50. Jung YJ, Hong SC, Seo DW, Hong SB: Surgical resection of cavernous angiomas located in eloquent areas--clinical research. Acta Neurochir Suppl; 2006;99:103-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Surgical resection of cavernous angiomas located in eloquent areas--clinical research.
  • In this retrospective study, our techniques for localizing lesion and the postoperative results of 26 patients with cavernous angiomas (CA) located at the eloquent areas are summarized.
  • [MeSH-major] Brain Neoplasms / surgery. Hemangioma, Cavernous / surgery

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  • (PMID = 17370774.001).
  • [ISSN] 0065-1419
  • [Journal-full-title] Acta neurochirurgica. Supplement
  • [ISO-abbreviation] Acta Neurochir. Suppl.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Austria
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51. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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52. 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

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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53. Menon V, Saxena R, Chaudhary Z: Pontine cavernous hemangioma presenting with horizontal gaze palsy. Indian J Pediatr; 2005 Jan;72(1):86

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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54. Matos M, Lorette G: [Angiomas and angiomatosis: Stewart-Bluefarb syndrome]. Ann Dermatol Venereol; 2007 Aug-Sep;134(8-9):704-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Angiomas and angiomatosis: Stewart-Bluefarb syndrome].
  • [Transliterated title] Angiomes et angiomatoses: syndrome de Stewart-Bluefarb.
  • [MeSH-major] Angiomatosis / diagnosis. Hemangioma / diagnosis. Skin Diseases / diagnosis. Skin Neoplasms / diagnosis
  • [MeSH-minor] Diagnosis, Differential. Diagnostic Imaging. Humans. Syndrome

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  • (PMID = 17925704.001).
  • [ISSN] 0151-9638
  • [Journal-full-title] Annales de dermatologie et de vénéréologie
  • [ISO-abbreviation] Ann Dermatol Venereol
  • [Language] fre
  • [Publication-type] Journal Article
  • [Publication-country] France
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55. Ikeda K, Hosozawa KI, Kashihara H, Kuratomi S, Kumazawa J, Shioikari M, Kuwajima A, Tamura M, Iwasaki Y: Familial cavernous angiomas. Neurology; 2005 Jan 11;64(1):163

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Familial cavernous angiomas.
  • [MeSH-major] Hemangioma, Cavernous / diagnosis. Hemangioma, Cavernous / genetics. Retinal Neoplasms / diagnosis. Retinal Neoplasms / genetics

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  • (PMID = 15642928.001).
  • [ISSN] 1526-632X
  • [Journal-full-title] Neurology
  • [ISO-abbreviation] Neurology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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56. Hamel-Teillac D: [Classification of angiomas]. Arch Pediatr; 2007 Jun;14(6):705-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Classification of angiomas].
  • [Transliterated title] Classification des angiomes.
  • [MeSH-major] Hemangioma / classification
  • [MeSH-minor] Blood Vessels / abnormalities. Child. Humans. Neoplasms, Vascular Tissue / classification. Ulcer / etiology

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  • (PMID = 17419037.001).
  • [ISSN] 0929-693X
  • [Journal-full-title] Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie
  • [ISO-abbreviation] Arch Pediatr
  • [Language] fre
  • [Publication-type] Journal Article
  • [Publication-country] France
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57. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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  • (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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58. Betlej M, Czepko R, Lopatka P, Danilewicz B, Uhl H: [Diagnosis and operative treatment cavernous angiomas of the central nervous system]. Przegl Lek; 2006;63(2):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] [Diagnosis and operative treatment cavernous angiomas of the central nervous system].
  • Among all detected cerebral angiomas the frequency of cavernous angiomas (CAs) is 5-13%.
  • [MeSH-major] Brain Neoplasms / diagnosis. Brain Neoplasms / surgery. Hemangioma, Cavernous, Central Nervous System / diagnosis. Hemangioma, Cavernous, Central Nervous System / surgery

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  • (PMID = 16967711.001).
  • [ISSN] 0033-2240
  • [Journal-full-title] Przegla̧d lekarski
  • [ISO-abbreviation] Prz. Lek.
  • [Language] pol
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Poland
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59. Maiuri F, Cappabianca P, Gangemi M, De Caro Mdel B, Esposito F, Pettinato G, de Divitiis O, Mignogna C, Strazzullo V, de Divitiis E: Clinical progression and familial occurrence of cerebral cavernous angiomas: the role of angiogenic and growth factors. Neurosurg Focus; 2006;21(1):e3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Clinical progression and familial occurrence of cerebral cavernous angiomas: the role of angiogenic and growth factors.
  • OBJECT: The authors studied the expression of angiogenic and growth factors and various proliferative indices in cavernous angiomas of the brain.
  • CONCLUSIONS: The familial occurrence and more aggressive clinical behavior of cavernous angiomas of the brain are associated with higher expression of Ki-67 and bcl-2 in the cavernoma tissue, as in other proliferative lesions.
  • [MeSH-major] Angiogenic Proteins / metabolism. Brain Neoplasms / physiopathology. Cerebral Veins / physiopathology. Growth Substances / metabolism. Hemangioma, Cavernous, Central Nervous System / physiopathology. Neovascularization, Pathologic / physiopathology
  • [MeSH-minor] Adolescent. Adult. Aged. Child. Child, Preschool. Disease Progression. Endothelial Cells / metabolism. Endothelial Cells / pathology. Female. Humans. Inheritance Patterns / genetics. Ki-67 Antigen / metabolism. Male. Middle Aged. Platelet-Derived Growth Factor / metabolism. Proto-Oncogene Proteins c-bcl-2 / metabolism. Tenascin / metabolism. Transforming Growth Factor beta / metabolism. Up-Regulation / physiology. Vascular Endothelial Growth Factor A / metabolism

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  • (PMID = 16859256.001).
  • [ISSN] 1092-0684
  • [Journal-full-title] Neurosurgical focus
  • [ISO-abbreviation] Neurosurg Focus
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Angiogenic Proteins; 0 / Growth Substances; 0 / Ki-67 Antigen; 0 / Platelet-Derived Growth Factor; 0 / Proto-Oncogene Proteins c-bcl-2; 0 / Tenascin; 0 / Transforming Growth Factor beta; 0 / Vascular Endothelial Growth Factor A
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60. Mirceva V, Hein R, Ring J, Möhrenschlager M: A case of multiple angiomas without any angiokeratomas in a female heterozygote with Fabry disease. Australas J Dermatol; 2010 Feb;51(1):36-8
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  • [Title] A case of multiple angiomas without any angiokeratomas in a female heterozygote with Fabry disease.
  • Fabry disease is a rare, X-chromosome-linked lysosomal storage disease caused by a deficient alpha-galactosidase A enzyme.
  • The disease manifests primarily in affected hemizygous males and to some extent in heterozygous females ('carrier').
  • A 45-year-old female Fabry disease patient without angiokeratomas but with numerous angiomas is presented.
  • An intrafamilial follow-up search detected a reduced leukocyte alpha-galactosidase A activity in her father, who suffered exclusively from coronary heart disease.
  • Our case report underlines the possible wide range of clinical signs in Fabry disease patients, sometimes complicated by missing typical lesions (e.g. angiokeratomas).
  • In oligosymptomatic Fabry disease cases, genetic analysis is recommended.
  • [MeSH-major] Fabry Disease / diagnosis. Hemangioma / diagnosis. Heterozygote Detection. Skin Neoplasms / diagnosis. alpha-Galactosidase / genetics
  • [MeSH-minor] Angiokeratoma / diagnosis. Angiokeratoma / genetics. Angiokeratoma / pathology. Female. Heterozygote. Humans. Leukocytes / enzymology. Male. Middle Aged

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  • (PMID = 20148840.001).
  • [ISSN] 1440-0960
  • [Journal-full-title] The Australasian journal of dermatology
  • [ISO-abbreviation] Australas. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
  • [Chemical-registry-number] EC 3.2.1.22 / alpha-Galactosidase
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61. Park SB, Jahng TA, Chung CK: The clinical outcomes after complete surgical resection of intramedullary cavernous angiomas: changes in motor and sensory symptoms. Spinal Cord; 2009 Feb;47(2):128-33

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] The clinical outcomes after complete surgical resection of intramedullary cavernous angiomas: changes in motor and sensory symptoms.
  • STUDY DESIGN: Evaluation of the surgical effects of patients with intramedullary spinal cord cavernous angiomas (CAs).
  • [MeSH-major] Hemangioma, Cavernous / physiopathology. Hemangioma, Cavernous / surgery. Neurosurgery / methods. Spinal Cord Neoplasms / physiopathology. Spinal Cord Neoplasms / surgery

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  • (PMID = 18663373.001).
  • [ISSN] 1362-4393
  • [Journal-full-title] Spinal cord
  • [ISO-abbreviation] Spinal Cord
  • [Language] eng
  • [Publication-type] Clinical Trial; Journal Article
  • [Publication-country] England
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62. Tohyama J, Akasaka N, Saito N, Kanazawa O, Morota N, Kameyama S: [An infant with multiple cavernous angiomas presenting with frequent epileptic seizures - detection of epileptic focus by magnetoencephalography]. No To Hattatsu; 2007 Jul;39(4):295-9
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  • [Title] [An infant with multiple cavernous angiomas presenting with frequent epileptic seizures - detection of epileptic focus by magnetoencephalography].
  • We report on a six-year-old girl with frequent partial seizures secondary to multiple cavernous angiomas (CAs) since the age of 17 months.
  • [MeSH-major] Brain / pathology. Brain Neoplasms / complications. Epilepsies, Partial / diagnosis. Epilepsies, Partial / etiology. Hemangioma, Cavernous / complications. Magnetoencephalography

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  • (PMID = 17633088.001).
  • [ISSN] 0029-0831
  • [Journal-full-title] No to hattatsu. Brain and development
  • [ISO-abbreviation] No To Hattatsu
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
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63. 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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64. Gamrot J, Bazowski P, Rudnik A, Zawadzki T: [Cavernous angiomas in the Department of Neurosurgery in Katowice]. Wiad Lek; 2005;58(11-12):595-7
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  • [Title] [Cavernous angiomas in the Department of Neurosurgery in Katowice].
  • There were 30 (18%) patients diagnosed as cavernous angioma (CA).
  • [MeSH-major] Brain Neoplasms / epidemiology. Hemangioma, Cavernous / epidemiology

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  • (PMID = 16594466.001).
  • [ISSN] 0043-5147
  • [Journal-full-title] Wiadomości lekarskie (Warsaw, Poland : 1960)
  • [ISO-abbreviation] Wiad. Lek.
  • [Language] pol
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Poland
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65. Santoro A, Piccirilli M, Bristot R, di Norcia V, Salvati M, Delfini R: Extradural spinal cavernous angiomas: report of seven cases. Neurosurg Rev; 2005 Oct;28(4):313-9
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  • [Title] Extradural spinal cavernous angiomas: report of seven cases.
  • The authors describe seven cases of extradural spinal cavernous angioma.
  • Although cavernoma itself is not rare, the extradural spinal localization is uncommon and makes preoperative differential diagnosis difficult.
  • Considering their rarity in this site, their presenting symptoms and the difficulties involved in neuroradiological diagnosis, the authors discuss the role of surgery as the principal form of treatment and review the relevant literature.
  • All patients had a CT scan, as well as MRI with gadolinium when possible, which detected an extradural roundish lesion: differential diagnosis was very difficult, especially between neurinoma and cavernoma.
  • In all cases histological diagnosis was cavernous angioma.
  • [MeSH-major] Hemangioma, Cavernous / pathology. Spinal Neoplasms / pathology

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  • (PMID = 15926084.001).
  • [ISSN] 0344-5607
  • [Journal-full-title] Neurosurgical review
  • [ISO-abbreviation] Neurosurg Rev
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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66. Tournier-Lasserve E: [Contribution of molecular genetics in cavernous angiomas]. Neurochirurgie; 2007 Jun;53(2-3 Pt 2):136-40

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Contribution of molecular genetics in cavernous angiomas].
  • [Transliterated title] Apports de la génétique moléculaire dans les angiomes caverneux.
  • In 20% of cases, central nervous system cavernomas are an autosomal dominant familial disease.
  • 2) in patients with multiple lesions who have an affected relative, the genetic nature of the disease is obvious and molecular tests are useful only for genetic counseling;.
  • 3) in sporadic cases with multiple lesions and no known affected relative, molecular tests can establish the genetic nature of the disease and be useful for genetic counseling.
  • [MeSH-major] Central Nervous System Neoplasms / genetics. Hemangioma, Cavernous, Central Nervous System / genetics. Molecular Biology

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  • (PMID = 17507048.001).
  • [ISSN] 0028-3770
  • [Journal-full-title] Neuro-Chirurgie
  • [ISO-abbreviation] Neurochirurgie
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] France
  • [Number-of-references] 31
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67. Boutarbouch M, Ben Salem D, Giré L, Giroud M, Béjot Y, Ricolfi F: Multiple cerebral and spinal cord cavernomas in Klippel-Trenaunay-Weber syndrome. J Clin Neurosci; 2010 Aug;17(8):1073-5
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  • Klippel-Trenaunay-Weber syndrome (KTWS) is a rare syndrome in which patients harbor cutaneous hemangiomas, venous varicosities, and osseous-soft tissue hypertrophy of the affected limb.
  • Similarly, the KRIT1 gene is involved in pathogenesis of cavernous angiomas.
  • We report a 55-year-old male with KTWS harboring multiple cavernous angiomas in the thoracic spinal cord and the brainstem, as revealed by MRI.
  • The rarity of cavernous angiomas in KTWS and the possibilities of shared genetic pathways between KTWS and cavernous angiomas are discussed.
  • [MeSH-major] Cerebral Cortex / pathology. Hemangioma, Cavernous, Central Nervous System / complications. Klippel-Trenaunay-Weber Syndrome / complications. Spinal Cord / pathology

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  • [Copyright] Copyright 2010 Elsevier Ltd. All rights reserved.
  • (PMID = 20493710.001).
  • [ISSN] 1532-2653
  • [Journal-full-title] Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
  • [ISO-abbreviation] J Clin Neurosci
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Scotland
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68. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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69. Samoilă O, Călugăru D, Călugăru M: [Clinical and fluorescein angiographic aspects in retinal angiomatosis (von Hippel)]. Oftalmologia; 2007;51(2):56-9
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  • Retinal angiomas represent a rare condition consisting of hamartomas isolated or associated with a systemic disease (Von Hippel-Lindau Disease).
  • We present a patient with multiple retinal angiomas, with atypical fluorescein angiography possible due to vascular thrombotic phenomena.
  • [MeSH-major] Angiomatosis / diagnosis. Fluorescein Angiography. Retinal Diseases / diagnosis. von Hippel-Lindau Disease / complications
  • [MeSH-minor] Diagnosis, Differential. Female. Humans. Middle Aged. Vision Disorders / etiology. Visual Acuity

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  • (PMID = 17937036.001).
  • [ISSN] 1220-0875
  • [Journal-full-title] Oftalmologia (Bucharest, Romania : 1990)
  • [ISO-abbreviation] Oftalmologia
  • [Language] rum
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Romania
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70. 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

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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71. Ficcadenti A, Santoro L, Petroni V, Carini C, Gabrielli O: Mental retardation, facial anomalies, brachydactyly, cerebral angiomas, femoral nucleus necrosis: a new entity or Hall-Riggs syndrome? Am J Med Genet A; 2009 May;149A(5):1001-5
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  • [Title] Mental retardation, facial anomalies, brachydactyly, cerebral angiomas, femoral nucleus necrosis: a new entity or Hall-Riggs syndrome?
  • We report on a 4-year-old boy with mental retardation, facial and skeletal anomalies, cerebral angiomas, femoral nucleus necrosis, mild biochemical abnormalities.
  • [MeSH-major] Brain Neoplasms / diagnosis. Central Nervous System Venous Angioma / diagnosis. Craniofacial Abnormalities / diagnosis. Facies. Femur / abnormalities. Fingers / abnormalities. Intellectual Disability / diagnosis. Osteonecrosis / diagnosis


72. Ozer E, Yücesoy K, Kalemci O: Demonstrated rapid growth of a corpus callosum cavernous angioma within a short period of time. J Neurosurg Sci; 2005 Dec;49(4):155-8; discussion 158
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  • [Title] Demonstrated rapid growth of a corpus callosum cavernous angioma within a short period of time.
  • Cavernous angiomas are uncommon central nervous system vascular malformations.
  • In this study we report a case of corpus callosum cavernous angioma which demonstrated rapid growth within a short period of time.
  • Corpus callosum cavernous angiomas have distinct features regarding growth and should be treated more carefully by giving more importance to surgical removal rather than a conservative approach.
  • [MeSH-major] Brain Neoplasms / pathology. Corpus Callosum / pathology. Hemangioma, Cavernous, Central Nervous System / pathology

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  • (PMID = 16374407.001).
  • [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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73. 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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  • [Cites] Neurol Med Chir (Tokyo). 2000 Nov;40(11):575-80 [11109795.001]
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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
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74. Martínez-Frías ML, Grupo de trabajo del ECEMC: Epidemiological association between isolated skin marks in newborn infants and single umbilical artery (SUA). Does it have biological plausibility? Am J Med Genet A; 2008 Jan 1;146A(1):26-34
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Using data from the Spanish Collaborative Study of Congenital Malformations (ECEMC), we analyzed "angiomas" (including all type of capillary skin marks, since it is not possible to distinguish it during the first 3 days of life), and nevi because they are the only defects detected in newborn infants as isolated skin defects.
  • In the ECEMC methodology, infants with nevi or angiomas as the only congenital defect are considered as cases when they present with only one of these skin marks measuring at least 1 cm in diameter and within the first 3 days of life, or when they have three or more such marks of any size.
  • A total sample of 1,832 consecutive newborn infants with isolated congenital skin marks was identified: 871 with nevi, 958 with angiomas, and 3 with both.
  • Newborn infants with SUA and isolated angiomas displayed higher birth measurements, and older maternal and paternal ages than newborn infants with angiomas and three umbilical vessels.
  • Similar results were observed when infants with angiomas and SUA were compared with control infants either with or without SUA.
  • The distribution of the angiomas by body areas, and sex preferences were also analyzed.
  • After evaluating the limitations and advantages of the present study, the results suggest that newborn infants with angiomas (irrespective of their type), SUA, and higher centile measurements may have one of the syndromes that exhibit this type of skin mark.
  • [MeSH-major] Congenital Abnormalities / epidemiology. Hemangioma / epidemiology. Nevus / epidemiology. Umbilical Arteries / abnormalities

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  • [Copyright] (c) 2007 Wiley-Liss, Inc.
  • (PMID = 17994564.001).
  • [ISSN] 1552-4833
  • [Journal-full-title] American journal of medical genetics. Part A
  • [ISO-abbreviation] Am. J. Med. Genet. A
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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75. Podobed OV, Konalenko VL: [Uterine arteriovenous anomaly in a young woman]. Arkh Patol; 2006 Jul-Aug;68(4):32-3
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  • The paper presents a case of uterine arteriovenous anomaly as mixed hamartoma with the signs of racemose and intramuscular angiomas, which was a morphological finding in an 18-year-old woman when the uterus removed for misdiagnosed postpartum septic endometritis was examined.
  • [MeSH-major] Arteriovenous Malformations / diagnosis. Uterine Neoplasms / diagnosis. Uterus / abnormalities. Uterus / blood supply

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  • (PMID = 16986494.001).
  • [ISSN] 0004-1955
  • [Journal-full-title] Arkhiv patologii
  • [ISO-abbreviation] Arkh. Patol.
  • [Language] rus
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Russia (Federation)
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76. Smith Pearl M, Abdalla WM, Lin DD, Comi AM, Boltshauser E, Gailloud P, Huisman TA: Sturge-Weber syndrome with cerebellar involvement. J Neuroradiol; 2009 Mar;36(1):57-60
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Sturge-Weber syndrome is a rare neurocutaneous disorder that typically presents with angiomas involving the face, ocular choroid and ipsilateral supratentorial leptomeninges.
  • [MeSH-major] Cerebellum / pathology. Magnetic Resonance Imaging / methods. Sturge-Weber Syndrome / diagnosis
  • [MeSH-minor] Child. Child, Preschool. Contrast Media. Diagnosis, Differential. Humans. Male

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  • (PMID = 18722014.001).
  • [ISSN] 0150-9861
  • [Journal-full-title] Journal of neuroradiology. Journal de neuroradiologie
  • [ISO-abbreviation] J Neuroradiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Contrast Media
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77. Chun SW, Kim SJ, Lee TH, Koo HS: Intra-root cavernous angioma of the cauda equina : a case report and review of the literature. J Korean Neurosurg Soc; 2010 Apr;47(4):291-4

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Intra-root cavernous angioma of the cauda equina : a case report and review of the literature.
  • Authors experienced intra-root cavernous angioma which is very rare case among cavernous angiomas of cauda equina.
  • Our intra-root cavernous angioma was confirmed by findings from operating field and microscopic examination.

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  • [Cites] Neurosurgery. 1995 Aug;37(2):195-204; discussion 204-5 [7477769.001]
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  • (PMID = 20461171.001).
  • [ISSN] 1598-7876
  • [Journal-full-title] Journal of Korean Neurosurgical Society
  • [ISO-abbreviation] J Korean Neurosurg Soc
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2864823
  • [Keywords] NOTNLM ; Cauda equina / Cavernous angioma / Intra-root cavernous angioma
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78. Kreusel KM, Bechrakis NE, Krause L, Neumann HP, Foerster MH: Retinal angiomatosis in von Hippel-Lindau disease: a longitudinal ophthalmologic study. Ophthalmology; 2006 Aug;113(8):1418-24
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Retinal angiomatosis in von Hippel-Lindau disease: a longitudinal ophthalmologic study.
  • OBJECTIVE: To characterize the clinical course of retinal angiomatosis (RA) in von Hippel-Lindau (VHL) disease.
  • PARTICIPANTS: Fifty-seven consecutive VHL disease patients with RA with a mean follow-up of 7.3 years.
  • METHODS: A retrospective chart review was performed to characterize the clinical course and functional outcome of RA to substantiate ophthalmic screening recommendations for VHL disease patients.
  • MAIN OUTCOME MEASURES: Age and visual acuity (VA) at diagnosis, angioma number, size, fundus position and growth behavior, functional outcome, and risk factors for adverse visual outcome (VA < or =20/1000) were evaluated.
  • Ocular disease was unilateral in 58% of patients at diagnosis; prevalence of bilateral RA as calculated by Kaplan-Meier analysis was 100% at age 56.4 years.
  • Risk factors included large angiomas at presentation, first manifestation at a younger age, and symptomatic RA.
  • In most eyes, development of new angiomas was slow and only small angiomas were detected on annual follow-up.
  • Eyes harboring multiple angiomas or RA complicated by retinal detachment were at risk of developing large angiomas after short follow-up intervals.
  • Formation of new angiomas was largely independent of patient age.
  • CONCLUSIONS: Retinal angiomatosis in VHL disease bears a high risk of severe vision loss at a young age.
  • In uncomplicated RA, annual ocular screening for presymptomatic angiomas is sufficient.
  • Because RA can occur at any age, lifelong ocular screening is recommended in VHL disease gene carriers starting at preschool age.
  • [MeSH-major] Angiomatosis / complications. Angiomatosis / physiopathology. Retinal Diseases / complications. Retinal Diseases / physiopathology. von Hippel-Lindau Disease / complications

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  • (PMID = 16769118.001).
  • [ISSN] 1549-4713
  • [Journal-full-title] Ophthalmology
  • [ISO-abbreviation] Ophthalmology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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79. Nishijima H, Nishimura S, Furuno Y, Kaimori M, Nishijima M: [A case of posttraumatic forehead cavernous angioma]. No Shinkei Geka; 2009 Sep;37(9):899-904
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  • [Title] [A case of posttraumatic forehead cavernous angioma].
  • Cavernous angiomas of the bone are rare tumors.
  • Most cavernous angiomas of the bone are congenital tumors.
  • In a review of the literature, we found only one case report of de novo generation of a skull cavernous angioma.
  • We present a case of a 25-year-old woman who had experienced a head injury, and 7 years later exhibited a skull tumor at the exact region of the injury.
  • Pathological findings showed a cavernous angioma-like lesion with some atypical details.
  • We finally diagnosed the lesion as a de novo cavernous angioma.
  • Our case suggests that fine injury may result in de novo generation of bone cavernomas.
  • [MeSH-major] Frontal Bone / injuries. Hemangioma, Cavernous / pathology. Skull Neoplasms / pathology

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  • (PMID = 19764425.001).
  • [ISSN] 0301-2603
  • [Journal-full-title] No shinkei geka. Neurological surgery
  • [ISO-abbreviation] No Shinkei Geka
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
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80. Yun TJ, Na DG, Kwon BJ, Rho HG, Park SH, Suh YL, Chang KH: A T1 hyperintense perilesional signal aids in the differentiation of a cavernous angioma from other hemorrhagic masses. AJNR Am J Neuroradiol; 2008 Mar;29(3):494-500
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A T1 hyperintense perilesional signal aids in the differentiation of a cavernous angioma from other hemorrhagic masses.
  • BACKGROUND AND PURPOSE: A cavernous angioma is a developmental vascular malformation with a high risk of hemorrhage.
  • The purpose of this work was to retrospectively determine whether an MR sign of T1 hyperintense perilesional signal intensity is useful for the differentiation of cavernous angioma from other hemorrhagic cerebral masses.
  • We retrospectively evaluated the MR images of 72 patients with acute or subacute cerebral hemorrhagic lesions with perilesional edema (29 cavernous angiomas, 13 glioblastomas, 1 oligodendroglioma, 16 metastatic tumors, and 13 intracerebral hemorrhages) for the presence of T1 hyperintense perilesional signal intensity.
  • In addition, T1 signal intensities of a perilesional edema were quantitatively analyzed.
  • In cavernous angiomas, volumes of hemorrhagic lesions and perilesional edemas, lesion locations, presence of contrast enhancement, and time intervals between symptom onset and MR imaging were also assessed.
  • RESULTS: T1 hyperintense perilesional signal intensity sign was found in 18 (62.1%) of 29 cavernous angiomas, in 1 (6.3%) of 16 metastases, and in 0 primary brain tumors or intracerebral hemorrhages.
  • Sensitivity, specificity, and positive predictive value of this sign for cavernous angioma were 62%, 98%, and 95%, respectively.
  • The perilesional T1 hyperintensity was significantly higher in cavernous angiomas (P = .045) than in normal white matter.
  • Perilesional edema volumes were larger in cavernous angiomas with the MR sign than in cavernous angiomas without the sign (P = .009).
  • CONCLUSION: When the MR sign of T1 hyperintense perilesional signal intensity is present, there is a high probability of cavernous angioma being present in the brain, and this MR sign may be helpful for differentiating cavernous angioma from hemorrhagic tumors and intracerebral hemorrhages.
  • [MeSH-major] Brain Neoplasms / diagnosis. Cerebral Hemorrhage / diagnosis. Hemangioma, Cavernous / diagnosis. Image Enhancement / methods. Magnetic Resonance Imaging / methods
  • [MeSH-minor] Adolescent. Adult. Aged. Child. Diagnosis, Differential. Female. Humans. Male. Middle Aged. Reproducibility of Results. Sensitivity and Specificity


81. 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
The Weizmann Institute of Science GeneCards and MalaCards databases. gene/protein/disease-specific - MalaCards for tufted angioma .

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  • [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


82. Gil C, Bellefleur JP, Vellin A, Leone M, Martin C: [Epidural analgesia and cutaneous angioma: need to perform MRI]. Ann Fr Anesth Reanim; 2010 Jan;29(1):48-9
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  • [Title] [Epidural analgesia and cutaneous angioma: need to perform MRI].
  • We wonder whether the use of magnetic resonance imaging (MRI) may be relevant for the detection of spinal angiomas in case of cutaneous angiomas.
  • The likelihood of finding a spinal angioma with MRI is low and the modus operandi is infrequently modified.
  • We report here a case of parturient with a cutaneous median angioma in the lumbar region, which was detected by MRI.
  • [MeSH-major] Analgesia, Epidural / methods. Analgesia, Obstetrical / methods. Hemangioma / pathology. Magnetic Resonance Imaging. Skin Neoplasms / pathology. Unnecessary Procedures

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  • [Copyright] Copyright 2009 Elsevier Masson SAS. All rights reserved.
  • (PMID = 20080013.001).
  • [ISSN] 1769-6623
  • [Journal-full-title] Annales françaises d'anesthèsie et de rèanimation
  • [ISO-abbreviation] Ann Fr Anesth Reanim
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] France
  • [Number-of-references] 8
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83. 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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84. Iza-Vallejo B, Mateo-Sierra O, Mosqueira-Centurión B, Ruíz-Juretschke F, Carrillo R: [Cerebral cavernomas. A review and update of aetiological, clinical and therapeutic features]. Rev Neurol; 2005 Dec 16-31;41(12):725-32
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  • INTRODUCTION: Cavernous angiomas are uncommon lesions, with a reported incidence of 0.4 to 0.8%, presenting a controversial management especially regarding their surgical treatment.
  • AIM: To update cavernous angiomas characteristics and management through a deep review of the literature concerning their aetiology, epidemiology, history, signs and symptoms, diagnosis, and surgical and radiosurgical treatment.
  • [MeSH-major] Brain Neoplasms. Hemangioma, Cavernous
  • [MeSH-minor] Diagnosis, Differential. Humans. Neurosurgery

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  • (PMID = 16355357.001).
  • [ISSN] 0210-0010
  • [Journal-full-title] Revista de neurologia
  • [ISO-abbreviation] Rev Neurol
  • [Language] spa
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Spain
  • [Number-of-references] 65
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85. Noez S, Collignon L, Bex V, Sacré F, Crielaard JM: [Kyphoplasty for the treatment of painful vertebral hemangioma]. Rev Med Liege; 2006 Feb;61(2):91-6
ORBi (University of Liege). Free full Text at ORBi .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Kyphoplasty for the treatment of painful vertebral hemangioma].
  • Vertebral angiomas are frequent and often asymptomatic.
  • Sometimes although they do not seem invasive radiologically, they are responsible for local pain.
  • If there is concordance between pain and vertebral angioma localisation, surgery such as vertebroplasty or cyphoplasty can be proposed.
  • [MeSH-major] Hemangioma / surgery. Orthopedic Procedures / methods. Spinal Neoplasms / surgery. Thoracic Vertebrae / surgery

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  • (PMID = 16566116.001).
  • [ISSN] 0370-629X
  • [Journal-full-title] Revue médicale de Liège
  • [ISO-abbreviation] Rev Med Liege
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Belgium
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86. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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87. Tomelleri G, Cappellari M, Di Matteo A, Zanoni T, Colato C, Bovi P, Moretto G: Blue rubber bleb nevus syndrome with late onset of central nervous system symptomatic involvement. Neurol Sci; 2010 Aug;31(4):501-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Blue rubber bleb nevus syndrome is a rare vascular disorder characterized by cavernous angiomas of skin and other organs including the gastrointestinal tract.
  • Here, we describe a case of 82-year-old patient presenting multiple skin haemangiomas for some years, who was admitted for a brain hemorrhage.
  • The MRI demonstrated the presence of multiple cavernous angiomas within the cerebral tissue.
  • [MeSH-major] Central Nervous System Diseases / etiology. Central Nervous System Diseases / pathology. Hemangioma, Cavernous, Central Nervous System / complications. Hemangioma, Cavernous, Central Nervous System / pathology. Nevus, Blue / complications. Nevus, Blue / pathology

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  • [Cites] Rom J Gastroenterol. 2004 Sep;13(3):237-40 [15470538.001]
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  • (PMID = 20352269.001).
  • [ISSN] 1590-3478
  • [Journal-full-title] Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
  • [ISO-abbreviation] Neurol. Sci.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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88. Gandhi M, Iyer H, Sehmbi H, Datir K: Anaesthetic management of a patient with sturge-weber syndrome undergoing oophorectomy. Indian J Anaesth; 2009 Feb;53(1):64-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Anaesthetic management of a patient with sturge-weber syndrome undergoing oophorectomy.
  • SUMMARY: The Sturge-Weber Syndrome (SWS) is a neurocutaneous disorder characterized by leptomeningeal and facial angiomas, neurologic and ocular manifestations.

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  • [Cites] Proc R Soc Med. 1929 Feb;22(4):431-442.5 [19986835.001]
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  • (PMID = 20640080.001).
  • [ISSN] 0976-2817
  • [Journal-full-title] Indian journal of anaesthesia
  • [ISO-abbreviation] Indian J Anaesth
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC2900036
  • [Keywords] NOTNLM ; Cerebro-Cortical Atrophy / Port Wine Angioma / Propofol / Sturge-Weber Syndrome
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89. Palleschi GM, Torchia D, Fabbri P: Blue rubber-bleb nevus syndrome: report of a case associated with osteoid osteomas. J Dermatol; 2005 Jul;32(7):589-93
MedlinePlus Health Information. consumer health - Skin Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Blue rubber-bleb nevus syndrome: report of a case associated with osteoid osteomas.
  • Blue rubber-bleb nevus syndrome (BRBNS), or Bean's syndrome, is a rare angiomatosis characterized by multiple cavernous hemangiomas of the skin, mucosae and frequently of other sites.
  • A 49-year-old male patient had been affected since birth by multiple angiomas localized in the skin, lips, oral cavity, cranial theca, and central nervous system; intrauterine rupture of angiomas in the right parietal lobe had caused partial hypotrophic paralysis of the left hemisoma.
  • [MeSH-major] Bone Neoplasms / pathology. Hemangioma / pathology. Neoplasms, Multiple Primary / pathology. Nevus, Blue / pathology. Osteoma, Osteoid / pathology. Skin Neoplasms / pathology


90. Gelal F, Feran H, Rezanko T, Vidinli BD: Giant cavernous angioma of the temporal lobe: a case report and review of the literature. Acta Radiol; 2005 May;46(3):310-3
MedlinePlus Health Information. consumer health - Brain Tumors.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Giant cavernous angioma of the temporal lobe: a case report and review of the literature.
  • Cavernous angiomas of the central nervous system are angiographically occult vascular lesions and are easily diagnosed by magnetic resonance imaging (MRI).
  • Giant cavernous angiomas (GCA) are rare, with only 11 cases reported in the literature.
  • Some GCAs have features that are similar to those of typical cavernous angiomas, whereas some lesions may be purely cystic; and some present with significant contrast enhancement and mass effect, mimicking neoplasms.
  • While the presence of hemosiderin, blood degradation products, and calcification may be helpful in the diagnosis of some cases, the correct diagnosis is not apparent until histopathological evaluation of the specimen is made in many instances.
  • [MeSH-major] Brain Neoplasms / diagnosis. Hemangioma, Cavernous / diagnosis. Temporal Lobe / pathology. Temporal Lobe / radiography
  • [MeSH-minor] Diagnosis, Differential. Female. Humans. Magnetic Resonance Imaging / methods. Middle Aged. Tomography, X-Ray Computed / methods

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  • (PMID = 15981729.001).
  • [ISSN] 0284-1851
  • [Journal-full-title] Acta radiologica (Stockholm, Sweden : 1987)
  • [ISO-abbreviation] Acta Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Sweden
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91. 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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92. Zapałowicz K, Radek M, Radek A, Błaszczyk B, Koziński T, Zelechowski J, Karnicki F, Myśliński R: Percutaneous vertebroplasty in the treatment of diseases causing vertebral bone loss. Ortop Traumatol Rehabil; 2005 Oct 30;7(5):499-504

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Percutaneous vertebroplasty in the treatment of diseases causing vertebral bone loss.
  • Between November 1999 and January 2005 the authors performed percutaneous vertebroplasty on 75 patients: 45 with osteoporotic compression fractures, 15 with angiomas of the vertebral bodies, and 12 patients with spinal neoplasms.
  • There were also 3 patients with coexisting spinal angiomas and osteoporotic compression fractures.
  • All these patients were treated under local anesthesia.
  • Filling with cement is effective in the treatment of osteoporotic compression fractures and of vertebral angiomas.

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  • (PMID = 17611442.001).
  • [ISSN] 1509-3492
  • [Journal-full-title] Ortopedia, traumatologia, rehabilitacja
  • [ISO-abbreviation] Ortop Traumatol Rehabil
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Poland
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93. Cortés JJ, Bernabé JM, Riera N, Arenas JJ: [Intracranial cavernous angioma.]. Radiologia; 2009 Mar-Apr;51(2):190-3
MedlinePlus Health Information. consumer health - Brain Tumors.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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94. Zakaria A, Lalani I, Belorgey L, Jay Foreman P: Focal occipital seizures with cerebral polyopia. Epileptic Disord; 2006 Dec;8(4):295-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Polyopia is the visual perception of multiple images of a single visual stimulus.
  • We report the case of a man with multiple cavernous angiomas and occipital lobe seizures manifesting as cerebral polyopia.

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  • (PMID = 17150444.001).
  • [ISSN] 1294-9361
  • [Journal-full-title] Epileptic disorders : international epilepsy journal with videotape
  • [ISO-abbreviation] Epileptic Disord
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
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95. Fortunato M, Di Pietro R, Gravina L, Maggi R, Ubaldi A, Vadalà P: Photodynamic therapy in von Hippel-Lindau disease in children. J Pediatr Ophthalmol Strabismus; 2009 Nov-Dec;46(6):376-9
MedlinePlus Health Information. consumer health - Von Hippel-Lindau Disease.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Photodynamic therapy in von Hippel-Lindau disease in children.
  • Von Hippel-Lindau disease is characterized by retinal hemangiomas that often produce hemorrhages and retinal detachment.
  • A 10-year-old boy with von Hippel-Lindau disease presenting with telangiectasias, endophytic angiomas, and exudative retinal detachment underwent treatment with retrobulbar steroid injection, laser photocoagulation, and photodynamic therapy, which led to improvement of visual acuity.
  • [MeSH-major] Photochemotherapy / methods. Photosensitizing Agents / therapeutic use. Porphyrins / therapeutic use. Retinal Detachment / drug therapy. von Hippel-Lindau Disease / drug therapy

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  • [Copyright] Copyright 2009, SLACK Incorporated.
  • (PMID = 19928746.001).
  • [ISSN] 0191-3913
  • [Journal-full-title] Journal of pediatric ophthalmology and strabismus
  • [ISO-abbreviation] J Pediatr Ophthalmol Strabismus
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Photosensitizing Agents; 0 / Porphyrins; 129497-78-5 / verteporfin
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96. Adam Z, Krikavová L, Krejcí M, Mechl M, Pour L, Moulis M, Vanícek J, Neumann C, Navrátil M, Veselý K, Vorlícek J: [Treatment of multiple angiomatosis involving the skeleton and the abdominal and thoracic cavities with interferon alpha, thalidomide and zoledronate]. Vnitr Lek; 2008 Jun;54(6):653-64
Hazardous Substances Data Bank. THALIDOMIDE .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Multiple angiomatosis is a very rare disease formed by histologically benign angiomas spreading beyond single organ or tissue.
  • In the case reported herein, hemangiomas affected several vertebrae of a young man and spread through his peritoneal cavity projecting to his stomach and causing recurrent hematemesis.
  • Even though the therapy eliminated bone pain after 2 months, CT check at a later stage showed but little regression of the mass of the angiomas in the abdominal cavity and the mediastinum.
  • Substantial reduction in the mass of the angiomas to merely residual quantity, i.e. partial remission of the disease, was achieved only after the addition of 100 mg/day thalidomide (Myrin) to the above mentioned doses of interferon and zoledronate administered on a regular basis.
  • However, the disease recurred after the therapy was interrupted, and the above triple combination therapy has had to be restored.
  • Maintenance therapy will succeed to repeated achievement of remission of angiomas.
  • [MeSH-major] Angiogenesis Inhibitors / administration & dosage. Angiomatosis / drug therapy. Diphosphonates / administration & dosage. Imidazoles / administration & dosage. Interferon-alpha / administration & dosage. Mediastinal Diseases / drug therapy. Peritoneal Diseases / drug therapy. Spinal Diseases / drug therapy. Thalidomide / administration & dosage
  • [MeSH-minor] Adult. Diagnosis, Differential. Drug Therapy, Combination. Humans. Male

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  • (PMID = 18672578.001).
  • [ISSN] 0042-773X
  • [Journal-full-title] Vnitr̆ní lékar̆ství
  • [ISO-abbreviation] Vnitr Lek
  • [Language] cze
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Czech Republic
  • [Chemical-registry-number] 0 / Angiogenesis Inhibitors; 0 / Diphosphonates; 0 / Imidazoles; 0 / Interferon-alpha; 4Z8R6ORS6L / Thalidomide; 6XC1PAD3KF / zoledronic acid
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97. Suprabha BS, Baliga M: Total oral rehabilitation in a patient with portwine stains. J Indian Soc Pedod Prev Dent; 2005 Jun;23(2):99-102
MedlinePlus Health Information. consumer health - Tooth Disorders.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Sturge-Weber syndrome is an uncommon condition characterized by presence of Portwine stains on the face along with ocular disorders, mental retardation, oral involvement and leptomeningeal angiomas.
  • A report of a case with atypical manifestations of this syndrome along with a step-by-step protocol oral rehabilitation of such patients is described.
  • [MeSH-major] Face. Mouth Rehabilitation. Port-Wine Stain / complications. Tooth Diseases / therapy
  • [MeSH-minor] Adolescent. Crowns. Dental Caries / therapy. Dental Plaque / prevention & control. Dental Restoration, Permanent. Female. Follow-Up Studies. Humans. Root Canal Therapy. Sturge-Weber Syndrome / diagnosis

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  • (PMID = 16012215.001).
  • [ISSN] 1998-3905
  • [Journal-full-title] Journal of the Indian Society of Pedodontics and Preventive Dentistry
  • [ISO-abbreviation] J Indian Soc Pedod Prev Dent
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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98. Bornfeld N, Kreusel KM: [Capillary hemangioma of the retina in cases of von Hippel-Lindau syndrome. New therapeutic directions]. Ophthalmologe; 2007 Feb;104(2):114-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Capillary hemangioma of the retina in cases of von Hippel-Lindau syndrome. New therapeutic directions].
  • Thermal photocoagulation of small peripheral angiomas is the treatment of choice for capillary hemangiomas in patients with von Hippel-Lindau disease.
  • Larger peripheral angiomas are better treated with beta-ray brachytherapy resulting in improved results in terms of local tumor control and the side effects of treatment.
  • Photodynamic treatment is an alternative option in the management of capillary hemangiomas of the retina.
  • The treatment of juxtapapillary angiomas is still a therapeutic dilemma.
  • [MeSH-major] Hemangioma, Capillary / therapy. Retinal Neoplasms / therapy. von Hippel-Lindau Disease

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  • (PMID = 17256181.001).
  • [ISSN] 0941-293X
  • [Journal-full-title] Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft
  • [ISO-abbreviation] Ophthalmologe
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Protons
  • [Number-of-references] 51
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99. Ruban JM, Baggio E: [Tumoral exophthalmitis]. J Fr Ophtalmol; 2009 Oct;32(8):600-9
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  • Generally, young people (0-20 years of age) will be affected mainly by benign diseases, such as angiomas or cysts (often dermoid cysts).
  • Adults (20-60 years of age) will for the most part develop benign tumors (cavernous hemangiomas, meningiomas) and inflammatory diseases.

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  • (PMID = 19853966.001).
  • [ISSN] 1773-0597
  • [Journal-full-title] Journal français d'ophtalmologie
  • [ISO-abbreviation] J Fr Ophtalmol
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
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100. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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