Document Detail


Klippel-Trenaunay syndrome and cerebral haemangiopericytoma: a potential association.
MedLine Citation:
PMID:  18297229     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Klippel-Trenaunay syndrome (KTS) a rare mesodermal phakomatosis consisting of capillary malformations, varicose veins, and limb hypertrophy, often associated with vascular malformations and benign tumours. A 33-year-old male presented with headaches secondary to a previously diagnosed intracranial tumour. He had a large blanching port-wine stain and hypertrophy of the left side of his body and limbs partial syndactyly of the 2(nd) and 3(rd) digits in all four extremities. The lesion was surgically resected and histology showed a Haemangiopericytoma. Thus KTS may be associated with intracranial Haemangiopericytomas, a malignant vascular tumour.
Authors:
M S Mathews; R C Kim; G Y Chang; M E Linskey
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Publication Detail:
Type:  Case Reports; Journal Article     Date:  2008-02-25
Journal Detail:
Title:  Acta neurochirurgica     Volume:  150     ISSN:  0942-0940     ISO Abbreviation:  Acta Neurochir (Wien)     Publication Date:  2008 Apr 
Date Detail:
Created Date:  2008-03-17     Completed Date:  2008-04-14     Revised Date:  2009-11-11    
Medline Journal Info:
Nlm Unique ID:  0151000     Medline TA:  Acta Neurochir (Wien)     Country:  Austria    
Other Details:
Languages:  eng     Pagination:  399-402; discussion 402     Citation Subset:  IM    
Affiliation:
Department of Neurological Surgery, University of California Irvine, Orange, CA, USA. mmathews@uci.edu
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MeSH Terms
Descriptor/Qualifier:
Adult
Combined Modality Therapy
Dura Mater* / pathology
Hemangiopericytoma / diagnosis*,  pathology,  therapy
Humans
Klippel-Trenaunay-Weber Syndrome / diagnosis*,  pathology,  therapy
Magnetic Resonance Imaging
Male
Meningeal Neoplasms / diagnosis*,  pathology,  therapy
Nerve Compression Syndromes / diagnosis,  pathology,  therapy
Neurologic Examination
Optic Nerve Diseases / diagnosis,  pathology,  surgery
Tomography, X-Ray Computed

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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