Renal Squamous Cell Carcinoma-related Polymyositis in a Patient with Autosomal Dominant Polycystic Kidney Disease

A 74-year-old Japanese woman diagnosed with autosomal dominant polycystic kidney disease (ADPKD) was admitted to our institute for the further examination of right-side groin pain developing in the past week. The patient was diagnosed with polymyositis (PM). Diagnostic imaging showed a mass lesion m...

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Autores principales: Terakawa, Kanako, Sawa, Naoki, Mizuno, Hiroki, Sekine, Akinari, Hayami, Noriko, Ikuma, Daisuke, Kawada, Masahiro, Hiramatsu, Rikako, Sumida, Keiichi, Yamanouchi, Masayuki, Hasegawa, Eiko, Suwabe, Tatsuya, Hoshino, Junichi, Kinowaki, Keiichi, Ohashi, Kenichi, Fujii, Takeshi, Ubara, Yoshifumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112967/
https://www.ncbi.nlm.nih.gov/pubmed/33853995
http://dx.doi.org/10.2169/internalmedicine.5375-20
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author Terakawa, Kanako
Sawa, Naoki
Mizuno, Hiroki
Sekine, Akinari
Hayami, Noriko
Ikuma, Daisuke
Kawada, Masahiro
Hiramatsu, Rikako
Sumida, Keiichi
Yamanouchi, Masayuki
Hasegawa, Eiko
Suwabe, Tatsuya
Hoshino, Junichi
Kinowaki, Keiichi
Ohashi, Kenichi
Fujii, Takeshi
Ubara, Yoshifumi
author_facet Terakawa, Kanako
Sawa, Naoki
Mizuno, Hiroki
Sekine, Akinari
Hayami, Noriko
Ikuma, Daisuke
Kawada, Masahiro
Hiramatsu, Rikako
Sumida, Keiichi
Yamanouchi, Masayuki
Hasegawa, Eiko
Suwabe, Tatsuya
Hoshino, Junichi
Kinowaki, Keiichi
Ohashi, Kenichi
Fujii, Takeshi
Ubara, Yoshifumi
author_sort Terakawa, Kanako
collection PubMed
description A 74-year-old Japanese woman diagnosed with autosomal dominant polycystic kidney disease (ADPKD) was admitted to our institute for the further examination of right-side groin pain developing in the past week. The patient was diagnosed with polymyositis (PM). Diagnostic imaging showed a mass lesion measuring 8 cm and a renal stone in the right kidney. Immediately following surgical resection of the right kidney, the patient's serum CK decreased to the normal range. A histopathological analysis showed well-differentiated squamous cell carcinoma. In conclusion, this case showed a close relationship between the occurrence of squamous cell carcinoma and the development of PM in an ADPKD patient.
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spelling pubmed-81129672021-05-18 Renal Squamous Cell Carcinoma-related Polymyositis in a Patient with Autosomal Dominant Polycystic Kidney Disease Terakawa, Kanako Sawa, Naoki Mizuno, Hiroki Sekine, Akinari Hayami, Noriko Ikuma, Daisuke Kawada, Masahiro Hiramatsu, Rikako Sumida, Keiichi Yamanouchi, Masayuki Hasegawa, Eiko Suwabe, Tatsuya Hoshino, Junichi Kinowaki, Keiichi Ohashi, Kenichi Fujii, Takeshi Ubara, Yoshifumi Intern Med Case Report A 74-year-old Japanese woman diagnosed with autosomal dominant polycystic kidney disease (ADPKD) was admitted to our institute for the further examination of right-side groin pain developing in the past week. The patient was diagnosed with polymyositis (PM). Diagnostic imaging showed a mass lesion measuring 8 cm and a renal stone in the right kidney. Immediately following surgical resection of the right kidney, the patient's serum CK decreased to the normal range. A histopathological analysis showed well-differentiated squamous cell carcinoma. In conclusion, this case showed a close relationship between the occurrence of squamous cell carcinoma and the development of PM in an ADPKD patient. The Japanese Society of Internal Medicine 2021-04-15 2021-04-15 /pmc/articles/PMC8112967/ /pubmed/33853995 http://dx.doi.org/10.2169/internalmedicine.5375-20 Text en Copyright © 2021 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Terakawa, Kanako
Sawa, Naoki
Mizuno, Hiroki
Sekine, Akinari
Hayami, Noriko
Ikuma, Daisuke
Kawada, Masahiro
Hiramatsu, Rikako
Sumida, Keiichi
Yamanouchi, Masayuki
Hasegawa, Eiko
Suwabe, Tatsuya
Hoshino, Junichi
Kinowaki, Keiichi
Ohashi, Kenichi
Fujii, Takeshi
Ubara, Yoshifumi
Renal Squamous Cell Carcinoma-related Polymyositis in a Patient with Autosomal Dominant Polycystic Kidney Disease
title Renal Squamous Cell Carcinoma-related Polymyositis in a Patient with Autosomal Dominant Polycystic Kidney Disease
title_full Renal Squamous Cell Carcinoma-related Polymyositis in a Patient with Autosomal Dominant Polycystic Kidney Disease
title_fullStr Renal Squamous Cell Carcinoma-related Polymyositis in a Patient with Autosomal Dominant Polycystic Kidney Disease
title_full_unstemmed Renal Squamous Cell Carcinoma-related Polymyositis in a Patient with Autosomal Dominant Polycystic Kidney Disease
title_short Renal Squamous Cell Carcinoma-related Polymyositis in a Patient with Autosomal Dominant Polycystic Kidney Disease
title_sort renal squamous cell carcinoma-related polymyositis in a patient with autosomal dominant polycystic kidney disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112967/
https://www.ncbi.nlm.nih.gov/pubmed/33853995
http://dx.doi.org/10.2169/internalmedicine.5375-20
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