Stewart Bluefarb syndrome: case report of a rare variant of acroangiodermatitis

Stewart Bluefarb syndrome is a rare acroangiodermatitis which occurs due to presence of arteriovenous malformations. It presents at birth or during early childhood as an erythematous to violaceous plaques over the dorsum of foot or ankle. It's a benign condition but can mimic a malignant condit...

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Bibliographic Details
Main Author: Guneet Awal (Author)
Format: Book
Published: Our Dermatology Online, 2018-07-01T00:00:00Z.
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520 |a Stewart Bluefarb syndrome is a rare acroangiodermatitis which occurs due to presence of arteriovenous malformations. It presents at birth or during early childhood as an erythematous to violaceous plaques over the dorsum of foot or ankle. It's a benign condition but can mimic a malignant condition, Kaposi's sarcoma. Histopathological differentiation between these two conditions is important. Investigations like doppler ultrasound are required to establish the diagnosis. In long standing cases, complications like ulceration, bleeding and secondary infections can occur. Treatment includes surgical correction of underlying arteriovenous malformation. 
546 |a EN 
546 |a ES 
546 |a FR 
546 |a PL 
690 |a Stewart Bluefarb syndrome 
690 |a Acroangiodermatitis 
690 |a Arteriovenous malformation 
690 |a Dermatology 
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786 0 |n Nasza Dermatologia Online, Vol 9, Iss 3, Pp 287-289 (2018) 
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