The Journal of the Korean Rheumatism Association 2008; 15(2): 165-169
Published online June 30, 2008
© Korean College of Rheumatology
허기훈ㆍ곽승기ㆍ박윤정ㆍ최진정*ㆍ조철수
가톨릭대학교 의과대학 성모병원 류마티스내과, 포천중문의과대학교 분당차병원 류마티스내과*
Correspondence to : Chul-Soo Cho
Antiphospholipid syndrome(APS) is characterized by vascular thrombosis in association with elevated titers of antiphospholipid antibodies. Leg ulcers are a considered to be a cutaneous manifestation of APS due to thrombosis of small to medium sized vessels. We report a case of necrotic non-healing, ankle ulcers mimicking pyoderma gangrenosum associated with APS in 50-year-old man. He had a past history of autoimmune thrombocytopenia and cerebral infarction. Laboratory findings showed a circulating lupus anticoagulant, positive anticardiolipin antibodies as well as anti-dsDNA and anti-Sm antibodies. Skin biopsy of ulcer lesions showed thrombotic vasculopathy of medium sized vessels with minimal leukocyte infiltration. Ulcers were successfully treated with surgical debridement and subsequent skin graft along with anticoagulation therapy.
Keywords Cutaneous ulceration, Antiphospholipid syndrome, Pyoderma gangrenosum, Systemic lupus erythematosus
The Journal of the Korean Rheumatism Association 2008; 15(2): 165-169
Published online June 30, 2008
Copyright © Korean College of Rheumatology.
허기훈ㆍ곽승기ㆍ박윤정ㆍ최진정*ㆍ조철수
가톨릭대학교 의과대학 성모병원 류마티스내과, 포천중문의과대학교 분당차병원 류마티스내과*
Ki-Hoon Hur, Seung-Ki Kwok, Yoon-Jung Park, Jin-Jung Choi*, Chul-Soo Cho
Division of Rheumatology, St. Mary's Hospital, School of Medicine, The Catholic University of Korea, Division of Rheumatology, CHA Hospital, College of Medicine, Pochon CHA University*, Seoul, Korea
Correspondence to:Chul-Soo Cho
Antiphospholipid syndrome(APS) is characterized by vascular thrombosis in association with elevated titers of antiphospholipid antibodies. Leg ulcers are a considered to be a cutaneous manifestation of APS due to thrombosis of small to medium sized vessels. We report a case of necrotic non-healing, ankle ulcers mimicking pyoderma gangrenosum associated with APS in 50-year-old man. He had a past history of autoimmune thrombocytopenia and cerebral infarction. Laboratory findings showed a circulating lupus anticoagulant, positive anticardiolipin antibodies as well as anti-dsDNA and anti-Sm antibodies. Skin biopsy of ulcer lesions showed thrombotic vasculopathy of medium sized vessels with minimal leukocyte infiltration. Ulcers were successfully treated with surgical debridement and subsequent skin graft along with anticoagulation therapy.
Keywords: Cutaneous ulceration, Antiphospholipid syndrome, Pyoderma gangrenosum, Systemic lupus erythematosus
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