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脾脏淀粉样变性:自发性脾破裂的罕见病因。

Splenic amyloidosis: a rare cause of spontaneous splenic rupture.

机构信息

Department of Diagnostic Imaging, Hospital Kuala Lumpur, Jalan Pahang, Kuala Lumpur 50586, Malaysia.

出版信息

Singapore Med J. 2011 Nov;52(11):e232-5.

Abstract

A 62 year-old woman who presented with an atraumatic acute abdomen was discovered to have haemoperitoneum with splenic rupture on urgent computed tomography and was immediately referred for life-saving emergency splenectomy. Histopathological examination revealed secondary splenic amyloidosis. The patient was later found to be suffering from infective endocarditis secondary to her permanent cardiac pacemaker. This report describes a patient who could have suffered from a long-standing infected vegetation on a permanent cardiac pacemaker, which led to splenic amyloidosis and spontaneous splenic rupture.

摘要

一位 62 岁女性因无创伤性急性腹痛就诊,紧急 CT 检查发现腹腔积血和脾破裂,立即转至普外科行紧急脾切除术。组织病理学检查显示继发性脾淀粉样变性。随后发现患者患有感染性心内膜炎,继发于她的永久性心脏起搏器。本报告描述了一位患者,她可能长期患有永久性心脏起搏器上的感染性赘生物,导致脾淀粉样变性和自发性脾破裂。

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