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Hereditary leiomyomatosis and renal cell cancer (HLRCC): A case report

Hereditary leiomyomatosis and renal cell cancer is a rare, inherited disease caused by mutations in the fumarate hydratase gene. It is characterized by cutaneous leiomyomas, uterine leiomyomas, and/or renal cell cancer. We present the case of a 42-year-old woman with a heterozygous missense mutation...

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Autores principales: Yonamine, Tomoko, Kaname, Tadashi, Chinen, Yasutsugu, Tamashiro, Kouichi, Kosuge, Noritake, Saito, Seiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052518/
https://www.ncbi.nlm.nih.gov/pubmed/32154112
http://dx.doi.org/10.1016/j.eucr.2020.101141
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author Yonamine, Tomoko
Kaname, Tadashi
Chinen, Yasutsugu
Tamashiro, Kouichi
Kosuge, Noritake
Saito, Seiichi
author_facet Yonamine, Tomoko
Kaname, Tadashi
Chinen, Yasutsugu
Tamashiro, Kouichi
Kosuge, Noritake
Saito, Seiichi
author_sort Yonamine, Tomoko
collection PubMed
description Hereditary leiomyomatosis and renal cell cancer is a rare, inherited disease caused by mutations in the fumarate hydratase gene. It is characterized by cutaneous leiomyomas, uterine leiomyomas, and/or renal cell cancer. We present the case of a 42-year-old woman with a heterozygous missense mutation (p.M195T) in the fumarate hydratase gene. Although the patient did not have cutaneous leiomyoma and she had no family history of hereditary leiomyomatosis and renal cell cancer, the presence of early onset symptomatic uterine leiomyoma and type 2 papillary renal cell cancer confirmed the diagnosis of hereditary leiomyomatosis and renal cell cancer.
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spelling pubmed-70525182020-03-09 Hereditary leiomyomatosis and renal cell cancer (HLRCC): A case report Yonamine, Tomoko Kaname, Tadashi Chinen, Yasutsugu Tamashiro, Kouichi Kosuge, Noritake Saito, Seiichi Urol Case Rep Oncology Hereditary leiomyomatosis and renal cell cancer is a rare, inherited disease caused by mutations in the fumarate hydratase gene. It is characterized by cutaneous leiomyomas, uterine leiomyomas, and/or renal cell cancer. We present the case of a 42-year-old woman with a heterozygous missense mutation (p.M195T) in the fumarate hydratase gene. Although the patient did not have cutaneous leiomyoma and she had no family history of hereditary leiomyomatosis and renal cell cancer, the presence of early onset symptomatic uterine leiomyoma and type 2 papillary renal cell cancer confirmed the diagnosis of hereditary leiomyomatosis and renal cell cancer. Elsevier 2020-02-26 /pmc/articles/PMC7052518/ /pubmed/32154112 http://dx.doi.org/10.1016/j.eucr.2020.101141 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Oncology
Yonamine, Tomoko
Kaname, Tadashi
Chinen, Yasutsugu
Tamashiro, Kouichi
Kosuge, Noritake
Saito, Seiichi
Hereditary leiomyomatosis and renal cell cancer (HLRCC): A case report
title Hereditary leiomyomatosis and renal cell cancer (HLRCC): A case report
title_full Hereditary leiomyomatosis and renal cell cancer (HLRCC): A case report
title_fullStr Hereditary leiomyomatosis and renal cell cancer (HLRCC): A case report
title_full_unstemmed Hereditary leiomyomatosis and renal cell cancer (HLRCC): A case report
title_short Hereditary leiomyomatosis and renal cell cancer (HLRCC): A case report
title_sort hereditary leiomyomatosis and renal cell cancer (hlrcc): a case report
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052518/
https://www.ncbi.nlm.nih.gov/pubmed/32154112
http://dx.doi.org/10.1016/j.eucr.2020.101141
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