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Stewart-Bluefarb syndrome associated with an iatrogenic arteriovenous fistula.
Nefrologia (Engl Ed)
September 2022
Servicio de Radiología, Hospital Universitario Severo Ochoa, Leganés (Madrid), Spain.
Acroangiodermatitis presenting as unilateral hypertrophic verrucous plaques.
Dermatol Online J
March 2022
Department of Internal Medicine, UTHealth McGovern Medical School, Houston, Texas, USA.
Acroangiodermatitis (AAD)[KL1] is a rare vasoproliferative disorder often involving the extremities that has been classified into two variants. Mali-type AAD is more common and associated with chronic venous stasis. Stewart-Bluefarb syndrome[KL2], the other variant, is associated with underlying arteriovenous abnormalities.
View Article and Find Full Text PDFStewart-Bluefarb syndrome following traumatic arteriovenous malformation.
Pediatr Dermatol
May 2021
Department of Dermatology, Liverpool Hospital, Liverpool, NSW, Australia.
Stewart-Bluefarb syndrome is a rare angioproliferative disorder that presents as violet plaques on the extremities, due to an underlying arteriovenous malformation (AVM). We report the case of a 12-year-old boy who developed a traumatic AVM in a bicycle accident and presented seven years later with exophytic, violet plaques. This is the first instance of a traumatic AVM preceding Stewart-Bluefarb syndrome in a pediatric patient in the literature.
View Article and Find Full Text PDFStewart-Bluefarb syndrome associated with an iatrogenic arteriovenous fistula.
Nefrologia (Engl Ed)
December 2020
Servicio de Radiología, Hospital Universitario Severo Ochoa, Madrid, España.
Acroangiodermatitis, Mali and Stewart-Bluefarb type: Two additional cases in adolescents.
Australas J Dermatol
February 2021
National Institute of Pathology (Indian Council of Medical Research), New Delhi, India.
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