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内膜中层黏液样动脉变性,一种具有法医学意义的罕见动脉疾病。

Intimomedial mucoid arterial degeneration, a rare arterial disorder of forensic significance.

作者信息

Wiskott Kim, Genet Pia, Lobrinus Johannes A, Fracasso Tony, Lardi Christelle

机构信息

University Center of Legal Medicine, Rue Michel-Servet 1, 1205, Geneva, Switzerland.

Clinical Pathology Division, Geneva University Hospitals, Rue Michel-Servet 1, 1205, Geneva, Switzerland.

出版信息

Forensic Sci Med Pathol. 2019 Dec;15(4):591-594. doi: 10.1007/s12024-019-00154-x. Epub 2019 Aug 24.

Abstract

The body of a 43-year-old African woman with a history of aortic aneurysm and hypertension was forensically investigated after her sudden death. The cause of death was related to a cardiac tamponade due to a ruptured aneurysm of the ascending aorta. Post-mortem gross examination showed an abnormal whitish discoloration of the intima with fibrous thickening of the aortic wall. Several arteries (left main and circumflex coronaries, carotid, renal and iliac arteries) showed similar features. Upon histological examination, the aortic aneurysm as well as the other arteries sampled showed mucoid degeneration, excess mucopolysaccharides and pools of mucin inside the intima and the media associated with collagen and elastic fiber destruction and loss of smooth muscle cells. This pattern strongly suggested the diagnosis of intimomedial mucoid degeneration (IMMD), a rare arterial disorder consisting of a progressive deposition of mucin into the intima and media, with a strong prevalence in middle-aged black African females with high blood pressure. In addition to the typical features of IMMD, histological examination of the ascending aorta showed a thickening of the adventita with sparse mixed inflammatory infiltrates and fibrosis, suggesting an additional chronic infectious aortitis. No infectious agent was detected. The body of literature on IMMD is reviewed and the origin of death is discussed in this case report.

摘要

一名有主动脉瘤和高血压病史的43岁非洲女性突然死亡后,其尸体进行了法医检查。死因与升主动脉瘤破裂导致的心包填塞有关。尸检大体检查显示内膜有异常的白色变色,主动脉壁纤维增厚。几条动脉(左冠状动脉主干和回旋支、颈动脉、肾动脉和髂动脉)表现出类似特征。组织学检查显示,主动脉瘤以及所取的其他动脉均表现为黏液样变性,内膜和中膜内有过多的黏多糖和黏液池,伴有胶原和弹性纤维破坏以及平滑肌细胞丢失。这种模式强烈提示诊断为内膜中层黏液样变性(IMMD),这是一种罕见的动脉疾病,其特征是黏液蛋白逐渐沉积到内膜和中膜,在患有高血压的中年非洲黑人女性中患病率较高。除了IMMD的典型特征外,升主动脉的组织学检查显示外膜增厚,有稀疏的混合性炎性浸润和纤维化,提示存在额外的慢性感染性主动脉炎。未检测到感染病原体。本文回顾了关于IMMD的文献,并在本病例报告中讨论了死亡原因。

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