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系统性硬化症患者因嗜铬细胞瘤引发的足趾坏死和急性心肌梗死

Toe necrosis and acute myocardial infarction precipitated by a pheochromocytoma in a patient with systemic sclerosis.

作者信息

Balbir-Gurman Alexandra, Menahem Nahir Abraham, Rozin Alexander, Markovits Doron, Braun-Moscovici Yolanda

机构信息

B. Shine Department of Rheumatology, Rambam Health Care Campus, Haifa, Israel.

出版信息

J Clin Rheumatol. 2007 Dec;13(6):331-3. doi: 10.1097/RHU.0b013e31815c1df8.

Abstract

Systemic sclerosis (SSc) patients typically experience Raynaud phenomena that is often complicated by digital ischemic lesions, gangrene, and digital loss. Other causes of peripheral ischemia, such as atherosclerosis, cryoglobulinemia, antiphospholipid syndrome, myeloproliferative disorders, paraneoplastic syndromes, and hyperadrenergic endocrine conditions, may be masked in SSc patients. We present a woman with limited SSc who developed toe necrosis and acute coronary events as a complication of a previously undiagnosed pheochromocytoma.

摘要

系统性硬化症(SSc)患者通常会出现雷诺现象,常并发指端缺血性病变、坏疽和指端缺失。外周缺血的其他原因,如动脉粥样硬化、冷球蛋白血症、抗磷脂综合征、骨髓增殖性疾病、副肿瘤综合征和高肾上腺素能内分泌疾病,在SSc患者中可能被掩盖。我们报告一例局限性SSc女性患者,其因先前未诊断出的嗜铬细胞瘤而并发足趾坏死和急性冠脉事件。

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