ホシノ ジユンイチ   Hoshino Jiyun'ichi
  星野 純一
   所属   医学部 医学科(東京女子医科大学病院)
   職種   教授・基幹分野長
論文種別 原著
言語種別 英語
査読の有無 査読なし
表題 常染色体優性多発性嚢胞腎患者における腸管穿孔からの腸管皮膚瘻の発生(Development of an enterocutaneous fistula from an intestinal perforation in a patient with autosomal dominant polycystic kidney disease)
掲載誌名 正式名:CEN Case Reports
ISSNコード:21924449
掲載区分国外
出版社 シュプリンガー・ジャパン(株)
巻・号・頁 12(1),pp.45-49
著者・共著者 Nakayama Yuki, Sawa Naoki, Suwabe Tatsuya, Sekine Akinari, Yamanouchi Masayuki, Ikuma Daisuke, Mizuno Hiroki, Oba Yuki, Hasegawa Eiko, Hoshino Junichi, Matoba Shuichiro, Ubara Yoshifumi
発行年月 2023/02
概要 We herein report a case of enterocutaneous fistula in a patient with autosomal dominant polycystic kidney disease (ADPKD). A 37-year-old Japanese man was admitted to our hospital. Three months prior to transfer to our hospital, he developed intense flank pain with gross hematuria. His serum creatinine had decreased to 7.8 mg/dL and hemodialysis was started, but gross hematuria persisted and he developed hypotension. Upon admission, plain chest radiography did not reveal any free air, but computed tomography (CT) showed generalized ventral subcutaneous air from the head to the lower extremities and enlarged kidneys. Enterography showed leakage of contrast medium from the descending colon into the subcutaneous area. C-reactive protein was 23.1 mg/dL. A colostomy was placed in the transverse colon proximal to the perforation, and systemic subcutaneous drainage was performed. The fever subsequently resolved, and the C-reactive protein test became negative. Three months later, renal artery embolization was performed, and 12 months thereafter, CT showed a marked decrease in kidney size. We assume that a markedly enlarged kidney leaded to intestinal perforation, which developed into an enterocutaneous fistula. Consequently, intestinal fluid leaked into the subcutaneous cavity of the abdominal wall and spread systemically, resulting in extensive subcutaneous abscesses.
DOI 10.1007/s13730-022-00716-z
文献番号 2024062468
PMID 35789990