DiFrancesco Lisa M, Burkart Peter, Hoehn James G
Division of Plastic Surgery, Albany Medical College, NY 12208, USA.
Ann Plast Surg. 2003 Nov;51(5):517-22. doi: 10.1097/01.SAP.0000058926.77448.9D.
Antiphospholipid antibody syndrome is a disease defined by the presence of a hypercoagulable clinical state in association with antiphospholipid antibodies. This syndrome can involve large-vessel thrombosis or thrombotic microangiopathy. Approximately 40% of patients will present with a cutaneous manifestation as the first indication of this disease, with a marked number of patients concurrently developing multiorgan involvement. The authors present a patient with extensive cutaneous necrosis-a devastating sequela of antiphospholipid antibody syndrome. Additionally, multiorgan involvement developed, requiring systemic anticoagulation and supportive care. When medically stable, plastic surgical intervention was necessary to treat extensive areas of cutaneous necrosis. Widespread cutaneous necrosis is a rare but known sequela of this syndrome. Studies have demonstrated that prophylaxis for thrombosis is not effective. However, long-term medical management with oral anticoagulants has been shown to reduce the risk of recurrent thrombosis. Occasionally, plastic surgical intervention is needed to treat the sequelae of this disease. Therefore, knowledge of the presentation and manifestations of this disease is critical in the early detection and prompt treatment of patients to prevent life-threatening consequences of this catastrophic disease process.
抗磷脂抗体综合征是一种由高凝临床状态与抗磷脂抗体同时存在所定义的疾病。该综合征可累及大血管血栓形成或血栓性微血管病。约40%的患者会以皮肤表现作为该病的首发症状,且有相当数量的患者同时并发多器官受累。作者报告了一例患有广泛皮肤坏死的患者——抗磷脂抗体综合征的一种严重后遗症。此外,还出现了多器官受累,需要进行全身抗凝和支持治疗。病情稳定后,需要进行整形外科干预来治疗大面积皮肤坏死。广泛皮肤坏死是该综合征一种罕见但已知的后遗症。研究表明,预防血栓形成无效。然而,口服抗凝剂的长期药物治疗已被证明可降低复发性血栓形成的风险。偶尔,需要进行整形外科干预来治疗该病的后遗症。因此,了解该疾病的表现对于早期发现和及时治疗患者以预防这种灾难性疾病过程的危及生命后果至关重要。