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结节性多动脉炎中的自发性脾破裂。

Spontaneous splenic rupture in polyarteritis nodosa.

作者信息

Ford G A, Bradley J R, Appleton D S, Thiru S, Calne R Y

出版信息

Postgrad Med J. 1986 Oct;62(732):965-6. doi: 10.1136/pgmj.62.732.965.

Abstract

A 28 year old man presented with haematuria and renal failure. Renal arteriography revealed bleeding into the pelvis of a solitary right kidney from a hilar artery. Multiple aneurysms were noted in the splenic artery. The spleen subsequently ruptured spontaneously and was removed at laparotomy together with the right kidney. Histological examination of the spleen and kidney revealed an acute necrotizing vasculitis involving medium-sized and smaller arteries confirming a diagnosis of polyarteritis nodosa. An area of infarction involved a subcapsular area of the spleen. Spontaneous splenic rupture is a rare but important complication of systemic vasculitides.

摘要

一名28岁男性出现血尿和肾衰竭。肾动脉造影显示,右侧孤立肾肾门动脉出血进入肾盂。脾动脉发现多个动脉瘤。随后脾脏自发破裂,在剖腹手术中与右肾一并切除。脾脏和肾脏的组织学检查显示,一种累及中、小动脉的急性坏死性血管炎,确诊为结节性多动脉炎。脾脏的一个包膜下区域出现梗死灶。自发性脾破裂是系统性血管炎罕见但重要的并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/2419066/c1554f07bf8a/postmedj00104-0058-a.jpg

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