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...

Descripción completa

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

Internet

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

Ejemplares similares