Literature DB >> 15730059

Spontaneous rupture of a left gastroepiploic artery aneurysm in a patient with autosomal-dominant polycystic kidney disease.

Y Nagaba1, H Nishimaki, M Ichinoe, Y Okuwaki, M Hamura, T Makino, T Sano, M Higashihara, K Kamata, K Soma.   

Abstract

Autosomal-dominant polycystic kidney disease (ADPKD) has been known to be associated with a variety of vascular diseases. We present a hemodialysis patient with ADPKD who died of a massive intraperitoneal hemorrhage caused by the spontaneous rupture of a left gastroepiploic artery aneurysm. A 64-year-old male was admitted to our hospital with acute upper abdominal pain and hemorrhagic shock. An abdominal angiography showed three aneurysms and the source of hemorrhage was assumed to be the left gastroepiploic artery aneurysm. The patient died of severe metabolic acidosis and disseminated intravascular coagulation (DIC) on the second hospital day. At autopsy, there was massive bleeding into the abdominal cavity, and pathological examination of the left gastroepiploic artery aneurysm revealed a dissecting aneurysm. This is the first case describing a rupture of a gastroepiploic aneurysm in a patient with ADPKD.

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Year:  2005        PMID: 15730059     DOI: 10.5414/cnp63163

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN: 0301-0430            Impact factor:   0.975


  3 in total

1.  Ruptured left gastroepiploic artery aneurysm - a diagnostic dilemma.

Authors:  Amith Kumar Choudhury; Shabuddin Khan; Graham Hoadley; Steve Pettit
Journal:  Indian J Surg       Date:  2008-07-30       Impact factor: 0.656

2.  Idiopathic Omental Bleeding Treated by Laparoscopic Partial Omentectomy: A Case Report and Review of the Literature.

Authors:  Shoryu Takayama; Koshiro Harata; Rei Mizuno; Riki Ganeko
Journal:  Cureus       Date:  2021-06-21

Review 3.  Spontaneous omental bleeding: a case report and literature review.

Authors:  Yun-Xiao Lyu; Yun-Xiao Cheng; Ting Li
Journal:  BMC Surg       Date:  2018-05-30       Impact factor: 2.102

  3 in total

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