Hanson Cody, Fischer Ryan, Fraga Garth, Rajpara Anand
University of Kansas Medical Center - Department of Dermatology.
Dermatol Online J. 2014 Nov 16;21(2):13030/qt0tp272d1.
Granulomatous pigmented purpuric dermatosis (PPD) is a rare subtype of pigmented purpuric dermatosis that is typically seen in women of Far East Asian descent on the distal lower extremities and feet. Granulomatous PPD is a benign condition that does not typically require treatment. Hyperlipidemia has been seen in over half of the eighteen cases reported in the literature. We report an unusual presentation of granulomatous PPD seen in a 71 year-old Caucasian female with hyperlipidemia.
肉芽肿性色素性紫癜性皮病（PPD）是色素性紫癜性皮病的一种罕见亚型，通常见于远东裔女性的下肢远端和足部。肉芽肿性PPD是一种良性疾病，通常不需要治疗。在文献报道的18例病例中，超过半数出现了高脂血症。我们报告了一例71岁患有高脂血症的白种女性患者出现的肉芽肿性PPD的不寻常表现。
