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常染色体显性多囊肾病伴麻痹性肠梗阻后外侧腹疝破裂。

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

作者信息

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

机构信息

Nephrology Center, Toranomon Hospital, Tokyo.

出版信息

Intern Med. 2005 Apr;44(4):311-4. doi: 10.2169/internalmedicine.44.311.

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.

摘要

我们报告了一名83岁的日本男性,患有常染色体显性多囊肾病(ADPKD),其特点是肾脏异常肿大,且在服用普鲁卡因胺后发生了肠梗阻。肠道肿胀并穿破皮肤,出现在皮肤外部。即使肠梗阻状态得到缓解,由于皮肤存在大的缺损,突出的肠道也未能恢复,因此进行了造口术。因肾脏肿大导致的包括侧腹疝在内的腹疝,可能会导致腹壁以及肠壁穿孔。

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