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抗磷脂抗体阳性患者中导致坏疽和截肢的周围血管闭塞。

Peripheral vascular occlusions leading to gangrene and amputations in antiphospholipid antibody positive patients.

作者信息

Asherson Ronald A, Cervera Ricard, Shoenfeld Yehuda

机构信息

Division of Immunology, School of Pathology, University of the Witwatersrand, Johannesburg, South Africa.

出版信息

Ann N Y Acad Sci. 2007 Jun;1108:515-29. doi: 10.1196/annals.1422.055.

Abstract

Twenty-one cases from several medical centers (Brazil, Italy, Serbia, South Africa, Israel, and the United Kingdom) with severe peripheral vascular disease progressing to amputations of limbs/digits, all of whom tested positive for antiphospholipid antibodies, are documented. The patients were suffering from either systemic lupus erythematosus, discoid LE, "primary" antiphospholipid syndrome (PAPS), "lupus-like" disease, undifferentiated connective tissue disease. A high frequency of livedo reticularis preceding the arterial occlusions in our series of patients who subsequently progressed to ischemic necrosis and amputation of limbs/digits was noted. Five of the 10 patients, in whom histopathological studies had been performed, demonstrated the typical vasculopathy seen with the antiphospholipid syndrome ("APS vasculopathy"). Complicating vasculitis was present in seven of the patients. Five of the patients developed severe peripheral vascular disease during the course of the catastrophic antiphospholipid (Asherson's) syndrome.

摘要

来自几个医疗中心(巴西、意大利、塞尔维亚、南非、以色列和英国)的21例患有严重外周血管疾病并进展至肢体/指趾截肢的病例被记录在案,所有这些患者抗磷脂抗体检测均呈阳性。这些患者患有系统性红斑狼疮、盘状红斑狼疮、“原发性”抗磷脂综合征(PAPS)、“狼疮样”疾病、未分化结缔组织病。在我们这组随后进展为缺血性坏死并肢体/指趾截肢的患者中,发现动脉闭塞之前出现网状青斑的频率很高。在10例进行了组织病理学研究的患者中,有5例表现出抗磷脂综合征所见的典型血管病变(“抗磷脂综合征血管病变”)。7例患者存在并发血管炎。5例患者在灾难性抗磷脂(阿舍尔森氏)综合征病程中出现严重外周血管疾病。

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