Hey A, Röckelein G
Institut für Pathologie, Universität Erlangen-Nürnberg.
Dtsch Med Wochenschr. 1987 Nov 20;112(47):1819-22. doi: 10.1055/s-2008-1068335.
In a 38-year-old woman, arterial hypertension was diagnosed a few weeks before her death. She died unexpectedly before a diagnostic clarification of the cause was possible. Autopsy revealed an arterial fibromuscular dysplasia with manifestation in both common iliac arteries, both renal arteries, the celiac trunk and the splenic artery. Both renal arteries displayed stenotic dissecant aneurysms which were the cause of the arterial hypertension. As a rare and lethal complication of fibromuscular dysplasia, a ruptured saccular aneurysm was found in the splenic artery. Histologically, the vascular alterations were a combination of medical fibromuscular dysplasia (type II) and periarterial or adventitial fibroplasia (type III). On the basis of the immunohistochemical detection of abundant lysozyme-positive cells, the periarterial fibroplasia appears to be a secondary chronic granulating and cicatricial reaction and not a separate form of fibromuscular dysplasia.
一名38岁女性在死亡前几周被诊断出患有动脉高血压。在对病因进行诊断性澄清之前,她意外死亡。尸检发现动脉纤维肌发育不良,累及双侧髂总动脉、双侧肾动脉、腹腔干和脾动脉。双侧肾动脉均显示狭窄性夹层动脉瘤,这是动脉高血压的病因。作为纤维肌发育不良罕见的致命并发症,在脾动脉中发现了一个破裂的囊状动脉瘤。组织学上,血管改变是医源性纤维肌发育不良(II型)和动脉周围或外膜纤维增生(III型)的组合。基于免疫组化检测到大量溶菌酶阳性细胞,动脉周围纤维增生似乎是一种继发性慢性肉芽形成和瘢痕形成反应,而不是纤维肌发育不良的一种单独形式。