| Literature DB >> 17927784 |
M Zutt1, S Emmert, I Moussa, E Haas, C Mitteldorf, H P Bertsch, C Neumann.
Abstract
We describe the rare Stewart-Bluefarb syndrome in a 15-year-old boy. This syndrome presents as a congenital arteriovenous malformation of the lower leg with multiple arteriovenous shunts accompanied by the benign acroangiodermatitis of Mali (pseudo-Kaposi's sarcoma). The clinical features of this disorder and the treatment options are reviewed.Entities:
Mesh：
Year: 2007 PMID： 17927784 DOI： 10.1111/j.1365-2230.2007.02541.x
Source DB: PubMed Journal: Clin Exp Dermatol ISSN： 0307-6938 Impact factor: 3.470