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A Case of Encapsulated Peritoneal Sclerosis Associated with a Ventriculo-Peritoneal Shunt Katsuhiko KONO 1 , Eiki WADA 1 , Tatsuya NISHIOKA 1 , Yuji KINUTA 1 , Yo MIZUKAMI 2 , Kenji FURUICHI 3 , Shigetaka SATO 4 1Department of Neurosurgery, Osaka Prefecture Saiseikai Noe Hospital 2Department of Gastroenterological Surgery, Osaka Prefecture Saiseikai Noe Hospital 3Department of Radiology, Osaka Prefecture Saiseikai Noe Hospital 4Department of Radiology, Shiga University of Medical Science Keyword: encapsulated peritoneal sclerosis , EPS , VP shunt , omental cyst , cerebrospinal pseudocyst , ileus pp.211-216
Published Date 2019/2/10
DOI https://doi.org/10.11477/mf.1436203919
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 We experienced a case of encapsulated peritoneal sclerosis(EPS)that developed as a result of peritoneal deterioration induced by ventriculo-peritoneal(VP)shunting. The patient was a 48-year-old man who underwent VP shunting five times since 1 month of age. Six months after the last operation, abdominal symptoms developed and the patient was hospitalized. A localized cyst was recognized in the left upper abdomen, and we diagnosed him with a cerebrospinal fluid pseudocyst. Soon, a shunt tube translocation was performed to another portion of the abdominal cavity, but a new short-term cyst appeared. During laparotomy, the inner surface of the abdominal cavity was very strong due to adhesions and the peritoneum was thickened. A large portion of the intestines and the mesentery was covered with a translucent film-like substance. Afterward, an ileus developed and he was diagnosed with EPS intraoperatively. We judged that an additional VP shunt was impossible, so a ventriculo-atrial shunt was placed. Afterward, his symptoms disappeared and the EPS improved. Although a few similar reports exist, this condition is thought to be extremely rare. Clinicians should recognize EPS as a complication of VP shunting.


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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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