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Parkes Weber syndrome presenting as Stewart-Bluefarb acroangiodermatitis
Reena Sharma1, Mudita Gupta1, Suresh Thakur2
1Department of Dermatology, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India.
Abstract:
Parkes Weber syndrome (PWS) is a rare disorder characterised by arteriovenous (AV) fistula, along with capillary, lymphatic, venous malformations and limb hypertrophy. Stewart-Bluefarb syndrome is a variant of acroangiodermatitis, which is associated with congenital AV malformation/fistulas. It usually begins early in life, unilaterally over lower extremities presenting as violaceous to dusky coloured macules, papules or plaques with tendency to ulcerate. We are reporting a case of AV malformation fulfilling the triad of PWS and presenting with acroangiodermatitis.
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