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[系统性红斑狼疮表现为皮质静脉血栓形成诱发的蛛网膜下腔出血,随后发生延髓内侧梗死]

[Systemic lupus erythematosus manifesting as subarachnoid hemorrhage induced by cortical venous thrombosis and followed by medial medullary infarction].

作者信息

Oshiro Shinya, Motomura Kazuhisa, Fukushima Takeo

机构信息

Department of Neurosurgery, Okinawa Prefectural Miyako Hospital, 807 Higashi-Nakasone, Hirara, Okinawa 906-0007, Japan.

出版信息

No To Shinkei. 2003 Sep;55(9):791-5.

Abstract

A 43-year-old female, who had been treated for systemic lupus erythematosus (SLE), presented with a subarachnoid hemorrhage (SAH) induced by rupture of cortical venous thrombosis, and be followed by medial medullary infarction during the acute stage of the SAH. The patient initially manifested a SAH. Angiography demonstrated no evidence of any aneurysms or arteriovenous malformations, but revealed cortical venous thrombosis. She suddenly developed left hemiplegia caused by medial medullary infarction on the 6th day. An active anticoagulant therapy was thought to be inappropriate because of initial symptoms as a hemorrhage. Since she had been accompanied by the medullary infarction, then, initially started by antiplatelet therapy. After the confirmation of no saccular or dissecting aneurysms with 2nd angiography, her treatment could be changed to anticoagulant therapy. Because of the sustained negative reactions of anti-cardiolipin beta 2 glycoprotein I antibody and lupus anticoagulant during the course of SLE, the definite diagnosis of antiphospholipid syndrome (APS) could not be made. However, this case is pathogenically thought to be cerebrovascular disease based upon APS, considering that this syndrome may be related to various antigen/antibody systems.

摘要

一名43岁女性,曾接受系统性红斑狼疮(SLE)治疗,因皮质静脉血栓破裂导致蛛网膜下腔出血(SAH),并在SAH急性期继发延髓内侧梗死。患者最初表现为SAH。血管造影未发现任何动脉瘤或动静脉畸形,但显示有皮质静脉血栓形成。她在第6天突然因延髓内侧梗死出现左侧偏瘫。由于最初表现为出血症状,积极的抗凝治疗被认为不合适。由于她伴有延髓梗死,因此最初开始采用抗血小板治疗。在第二次血管造影证实没有囊状或夹层动脉瘤后,她的治疗可改为抗凝治疗。由于在SLE病程中抗心磷脂β2糖蛋白I抗体和狼疮抗凝物持续呈阴性反应,无法明确诊断抗磷脂综合征(APS)。然而,考虑到该综合征可能与各种抗原/抗体系统有关,该病例在病因上被认为是基于APS的脑血管疾病。

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