Literature DB >> 15897642

Autosomal dominant polycystic kidney disease showing rupture of a lateral ventral hernia following paralytic ileus.

Takashi Kato1, Yoshifumi Ubara, Tetsuo Tagami, Naoki Sawa, Junichi Hoshino, Tatsuya Suwabe, Takaaki Yamagata, Hideyuki Katori, Fumi Takemoto, Shigeko Hara, Shuichirou Matoba, Kenmei Takaichi.   

Abstract

We report an 83-year-old Japanese male with autosomal dominant polycystic kidney disease (ADPKD), which was marked by unusually enlarged kidneys, and in whom ileus occurred after administration of procainamide. The bowels became swollen and ruptured the skin and appeared on the outside of the skin. Even after the ileus state was resolved, the projected intestinal tract was not restored due to a large defect of the skin, and ostomy was performed. Abdominal hernia including lateral ventral hernia due to enlarged kidneys may result in perforation of the abdominal wall as well as intestinal wall.

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Year:  2005        PMID: 15897642     DOI: 10.2169/internalmedicine.44.311

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  2 in total

1.  Development of an enterocutaneous fistula from an intestinal perforation in a patient with autosomal dominant polycystic kidney disease.

Authors:  Yuki Nakayama; Naoki Sawa; Tatsuya Suwabe; Akinari Sekine; Masayuki Yamanouchi; Daisuke Ikuma; Hiroki Mizuno; Yuki Oba; Eiko Hasegawa; Junichi Hoshino; Shuichiro Matoba; Yoshifumi Ubara
Journal:  CEN Case Rep       Date:  2022-07-05

2.  Percutaneous Nephrolithotomy in Autosomal Dominant Polycystic Kidney Disease: Is it Different from Percutaneous Nephrolithotomy in Normal Kidney?

Authors:  Vishwajeet Singh; Rahul Janak Sinha; Dheeraj Kumar Gupta
Journal:  Curr Urol       Date:  2013-07-28
  2 in total

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