| Huge multilobular cavernous angioma in an infant: case report. | |
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MedLine Citation:
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PMID: 8327078 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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The authors encountered a rare case of multilobular cavernous angioma arising from the paraventricular region in an infant. Total resection of the angioma, which was 8 cm in diameter, was performed. The patient showed no neurological deficit. Although 22 cases in infants have previously been reported, this is the largest cavernous angioma and it is especially rare because of its multilobular configuration. |
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Authors:
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J Kawagishi; M Suzuki; T Kayama; T Yoshimoto |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Neurosurgery Volume: 32 ISSN: 0148-396X ISO Abbreviation: Neurosurgery Publication Date: 1993 Jun |
Date Detail:
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Created Date: 1993-08-06 Completed Date: 1993-08-06 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 7802914 Medline TA: Neurosurgery Country: UNITED STATES |
Other Details:
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Languages: eng Pagination: 1028-30; discussion 1030-1 Citation Subset: IM |
Affiliation:
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Division of Neurosurgery, Tohoku University School of Medicine, Sendai, Japan. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Brain
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pathology Brain Neoplasms / congenital*, diagnosis, pathology, surgery Cephalometry Cerebral Angiography Cerebral Hemorrhage / congenital, diagnosis, pathology, surgery Craniotomy Endothelium, Vascular / pathology Hemangioma, Cavernous / congenital*, diagnosis, pathology, surgery Humans Infant Magnetic Resonance Imaging Male Tomography, X-Ray Computed |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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