Sharma Reena, Gupta Mudita, Thakur Suresh, Gupta Archit
Department of Dermatology, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India.
Department of Radiodiagnosis, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India.
BMJ Case Rep. 2019 Mar 8;12(3):e227793. doi: 10.1136/bcr-2018-227793.
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.
帕克斯·韦伯综合征（PWS）是一种罕见的疾病，其特征为动静脉（AV）瘘，同时伴有毛细血管、淋巴管、静脉畸形以及肢体肥大。斯图尔特 - 布卢法布综合征是肢端血管性皮炎的一种变体，与先天性动静脉畸形/瘘相关。它通常在生命早期开始，单侧出现在下肢，表现为紫蓝色至暗褐色的斑疹、丘疹或斑块，并有溃疡倾向。我们报告一例符合PWS三联征并伴有肢端血管性皮炎的动静脉畸形病例。
