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色素性紫癜性皮病与原发性抗磷脂综合征相关。

Pigmented purpuric dermatosis associated with primary antiphospholipid syndrome.

作者信息

Yildiz Fatih, Tas Didem Arslan, Açikalin Arbil, Karakas Tugba, Kalyoncu Umut, Erken Eren

机构信息

Department of Rheumatology-Immunology, Cukurova University Faculty of Medicine, Turkey.

出版信息

Intern Med. 2013;52(11):1255-7. doi: 10.2169/internalmedicine.52.0028.

Abstract

Pigmented purpuric dermatosis (PPD) is a group of chronic disorders characterized by the extravasation of erythrocytes and marked hemosiderin deposits in the dermis. Schamberg disease is a subtype of pigmented purpuric dermatosis in which nonpalpable purpura is prominent on the lower extremities. No cases of primary antiphospholipid syndrome and pigmented purpuric dermatosis have so far been reported in the literature. We herein report a case of pigmented purpuric dermatosis associated with primary antiphospholipid syndrome.

摘要

色素性紫癜性皮病(PPD)是一组以红细胞外渗和真皮内明显含铁血黄素沉积为特征的慢性疾病。尚伯格病是色素性紫癜性皮病的一种亚型,其特征为下肢出现不可触及的紫癜。目前文献中尚未报道原发性抗磷脂综合征与色素性紫癜性皮病相关的病例。我们在此报告一例原发性抗磷脂综合征相关的色素性紫癜性皮病病例。

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