Stewart-Bluefarb syndrome revisited.

Abstract:

:Stewart-Bluefarb syndrome (SBS) is a subtype of pseudo-Kaposi sarcoma (PKS), which is associated with congenital arteriovenous malformation. It is a rare syndrome, characterized by cutaneous lesions with onset in the second decade of life. We report a case of SBS in a 33-year-old man presenting with a 15-year history of unilateral, reddish-brown, raised lesions on his right lower leg and the dorsum of his foot. Diagnosis of PKS was confirmed by histopathology and radiology. We report the clinical features, aetiopathogenesis, differential diagnosis and treatment of this rare condition.

journal_name

Clin Exp Dermatol

authors

Verma SB,Vasani R

doi

10.1111/ced.12839

subject

Has Abstract

pub_date

2016-07-01 00:00:00

pages

522-5

issue

5

eissn

0307-6938

issn

1365-2230

journal_volume

41

pub_type

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