Anti-phospholipid antibody syndrome with skin as a primary involved organ: an interesting case report

Aum N. Soni, Harshad V. Parmar, Hinal J. Prajapati
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Abstract

Anti-phospholipid antibody (APLA) syndrome is a multisystem vascular thrombopathy characterized by presence of antibodies against phospholipid antigens. Resulting thrombosis due to these antibodies leads to hallmark obstetric complications, cutaneous and cerebral vascular involvement, pulmonary embolism and thrombosis which can occur in vasculature of any organ system of body. Though APLA syndrome is characterized by pregnancy loss and foetal morbidity, isolated cutaneous or other system presentation has been reported especially in male patients. Here we present an interesting case report of an old aged male patient presenting with cutaneous ulcers and skin involvement as presenting feature.
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以皮肤为主要受累器官的抗磷脂抗体综合征:一份有趣的病例报告
抗磷脂抗体(APLA)综合征是一种多系统血管血栓病,其特点是存在针对磷脂抗原的抗体。这些抗体导致的血栓形成可引起产科并发症、皮肤和脑血管受累、肺栓塞和血栓形成,可发生在身体任何器官系统的血管中。虽然APLA综合征的特点是妊娠失败和胎儿发病率高,但也有报道称其表现为孤立的皮肤或其他系统受累,尤其是男性患者。我们在此报告了一例有趣的病例,患者是一名老年男性,以皮肤溃疡和皮肤受累为主要特征。
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