Recurrent Myelopathy in a Patient with Klippel-Trenaunay Syndrome / 대한임상신경생리학회지
Korean Journal of Clinical Neurophysiology
;
: 76-79, 2015.
Article
in Korean
| WPRIM
| ID: wpr-215704
ABSTRACT
Klippel-Trenaunay syndrome (KTS) is a rare congenital malformation syndrome involving blood and lymph vessels, which is characterized by triad of cutaneous hemangioma, venous varicosities, and overgrowth of the affected limbs. Because vascular malformation in KTS can be located anywhere except the face and brain, the clinical presentation could be extremely variable. But there are only rare case reports that KTS is associated with spinal cord lesion. We report a case of recurrent myelopathy in a patient with KTS.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Spinal Cord
/
Spinal Cord Diseases
/
Brain
/
Klippel-Trenaunay-Weber Syndrome
/
Extremities
/
Vascular Malformations
/
Hemangioma
Limits:
Humans
Language:
Korean
Journal:
Korean Journal of Clinical Neurophysiology
Year:
2015
Type:
Article
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