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狼疮伴继发性抗磷脂综合征的自发性脾动脉出血:一例报告

Spontaneous splenic artery hemorrhage with secondary antiphospholipid syndrome in lupus: a case report.

作者信息

Itagaki M W, Gregory J S

机构信息

University of Illinois, College of Medicine at Urbana-Champaign, Urbana, Illinois 61801, USA.

出版信息

Lupus. 2005;14(6):479-82. doi: 10.1191/0961203305lu2089cr.

Abstract

Spontaneous hemorrhage is a rare complication of lupus. We describe a 36-year old female with lupus who suffered spontaneous, nontraumatic hemorrhage from branches of the splenic artery with massive blood loss while being treated for a lupus flare. We compare this to the two other reported cases of similar lupus-associated splenic artery hemorrhage documented in the literature, both of which had significant pre-existing hemorrhagic risk factors. Spontaneous, nontraumatic hemorrhage of the splenic artery in the absence of risk factors, and in a patient with secondary antiphospholipid syndrome, has been previously undescribed in lupus.

摘要

自发性出血是狼疮的一种罕见并发症。我们描述了一名36岁的狼疮女性患者,在狼疮病情活动接受治疗时,出现了脾动脉分支的自发性、非创伤性出血,并伴有大量失血。我们将此病例与文献中报道的另外两例类似的狼疮相关性脾动脉出血病例进行比较,这两例均有明显的既往出血危险因素。在没有危险因素的情况下,以及在一名继发性抗磷脂综合征患者中出现脾动脉自发性、非创伤性出血,此前在狼疮中尚未有过描述。

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