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

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 creatini...

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Detalles Bibliográficos
Autores principales:	Nakayama, Yuki, Sawa, Naoki, Suwabe, Tatsuya, Sekine, Akinari, Yamanouchi, Masayuki, Ikuma, Daisuke, Mizuno, Hiroki, Oba, Yuki, Hasegawa, Eiko, Hoshino, Junichi, Matoba, Shuichiro, Ubara, Yoshifumi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Nature Singapore 2022
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892373/ https://www.ncbi.nlm.nih.gov/pubmed/35789990 http://dx.doi.org/10.1007/s13730-022-00716-z

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