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一名患有缺血性中风的西班牙裔男性同时存在原发性抗磷脂综合征和蛋白S缺乏症。

Coexistence of primary antiphospholipid syndrome and protein S deficiency in a Hispanic man with ischemic stroke.

作者信息

Reyes-Iglesias Y, Ortiz A A, Goitía D M, Meléndez R

机构信息

Department of Medicine, Veterans Administration Medical Center and University of Puerto Rico School of Medicine, San Juan, USA.

出版信息

South Med J. 1998 Mar;91(3):296-8. doi: 10.1097/00007611-199803000-00020.

Abstract

The primary antiphospholipid syndrome and protein S deficiency are known hypercoagulable states predisposing to ischemic strokes. The pathogenesis of those hypercoagulable states has been independently studied and, recently, interaction between them has been proposed. A 48-year-old Hispanic man had generalized seizures 5 months after the acute onset of a left middle cerebral artery infarct. He had a strong family history of strokes. After evaluation for cardiologic, rheumatologic, hematologic and metabolic etiologies for stroke, anticardiolipin antibodies and protein S deficiency were detected. Cerebral angiography was normal. First degree relatives were evaluated and screened for these conditions. Lupus anticoagulant was detected in a sister who reported a transient hemisensory deficit. None of the relatives studied had clinical or laboratory criteria for collagen vascular diseases. Coexistence of the primary antiphospholipid syndrome and protein S deficiency, two known prothrombotic states, has rarely been reported in Hispanic adults in association with ischemic stroke.

摘要

原发性抗磷脂综合征和蛋白S缺乏是已知的易导致缺血性中风的高凝状态。这些高凝状态的发病机制已分别进行了研究,最近有人提出它们之间存在相互作用。一名48岁的西班牙裔男性在左大脑中动脉梗死急性发作5个月后出现全身性癫痫发作。他有很强的中风家族史。在对中风的心脏、风湿、血液和代谢病因进行评估后,检测到抗心磷脂抗体和蛋白S缺乏。脑血管造影正常。对其一级亲属进行了这些情况的评估和筛查。在一名报告有短暂性半侧感觉障碍的姐妹中检测到狼疮抗凝物。所研究的亲属中没有一人符合胶原血管疾病的临床或实验室标准。原发性抗磷脂综合征和蛋白S缺乏这两种已知的促血栓形成状态并存,在西班牙裔成年人中与缺血性中风相关的情况鲜有报道。

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