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[自发性肾破裂——结节性多动脉炎的一种并发症]

[Spontaneous kidney ruptures--a complication of panarteritis nodosa].

作者信息

Brkovic D, Möhring K, Nöldge G, Dörsam J, Kälble T, Pomer S, Staehler G

机构信息

Urologische Abteilung, Chirurgischen Universitätsklinik Heidelberg.

出版信息

Urologe A. 1995 Nov;34(6):470-4.

PMID:8848859
Abstract

Besides renal cell carcinomas and angiomyolipomas panarteritis nodosa (PAN) is a common underlying disorder for spontaneous perirenal hematomas (SPH). Herein we report on 3 cases with PAN associated kidney ruptures where diagnosis of PAN was not known before in 2 instances. The hematoma was identified by computerized tomography (CT) in all patients, nevertheless CT failed to reveal the underlying disorder in any case. In this situation angiography was extremely valuable visualizing multiple renal microaneurysms that are typical for PAN. Operative exploration and drainage of the hematoma was necessary in two patients because of hemodynamic instability. In one patient bleeding could be controlled after an immediate immunosuppressive therapy with prednisone and cyclophosphamide. Due to the high incidence of PAN associated spontaneous perirenal hematomas angiography should be performed in all cases with unclear SPH after CT evaluation. In our opinion an immediate surgical intervention is only indicated in cases with hemodynamic instability. Otherwise a conservative approach including immediate immunosuppression seems justified. Nephrectomy should be avoided whenever possible.

摘要

除肾细胞癌和血管平滑肌脂肪瘤外,结节性多动脉炎(PAN)是自发性肾周血肿(SPH)常见的潜在病因。在此,我们报告3例与PAN相关的肾破裂病例,其中2例之前未确诊PAN。所有患者均通过计算机断层扫描(CT)发现血肿,但CT均未能揭示潜在病因。在这种情况下,血管造影对于显示PAN典型的多发性肾微动脉瘤极为有价值。由于血流动力学不稳定,2例患者需要进行手术探查和血肿引流。1例患者在立即使用泼尼松和环磷酰胺进行免疫抑制治疗后出血得到控制。鉴于PAN相关自发性肾周血肿的高发生率,在CT评估后所有不明原因的SPH病例均应进行血管造影。我们认为,仅在血流动力学不稳定的情况下才需要立即进行手术干预。否则,包括立即免疫抑制在内的保守方法似乎是合理的。应尽可能避免肾切除术。

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