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Concurrent renal-cell carcinoma and cutaneous leiomyomas: A case of HLRCC

A 51-year-old Caucasian female presenting with renal-cell cancer and cutaneous leiomyomas was later diagnosed with Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) Syndrome. HLRCC is an autosomal dominant condition caused by a mutation in the fumarate hydratase gene, which encodes for an enzy...

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Autores principales: Fondriest, Sara A., Gowdy, John M., Goyal, Manish, Sheridan, Katherine C., Wasdahl, Daniel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921156/
https://www.ncbi.nlm.nih.gov/pubmed/27408652
http://dx.doi.org/10.2484/rcr.v10i1.962
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author Fondriest, Sara A.
Gowdy, John M.
Goyal, Manish
Sheridan, Katherine C.
Wasdahl, Daniel A.
author_facet Fondriest, Sara A.
Gowdy, John M.
Goyal, Manish
Sheridan, Katherine C.
Wasdahl, Daniel A.
author_sort Fondriest, Sara A.
collection PubMed
description A 51-year-old Caucasian female presenting with renal-cell cancer and cutaneous leiomyomas was later diagnosed with Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) Syndrome. HLRCC is an autosomal dominant condition caused by a mutation in the fumarate hydratase gene, which encodes for an enzyme in the citric acid cycle. This syndrome has been reported in over 100 families throughout the world, the majority of whom are of Eastern European descent. Those with this syndrome have a significantly increased risk of developing renal-cell carcinoma, cutaneous leiomyomas, and uterine leiomyomas, and a smaller chance of developing uterine leiomyosarcomas. This syndrome has a relatively poor prognosis, with tumor metastasis occurring in approximately 50% of patients. However, more aggressive prophylactic measures and recent studies have shown potential to improve patient prognosis.
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spelling pubmed-49211562016-07-12 Concurrent renal-cell carcinoma and cutaneous leiomyomas: A case of HLRCC Fondriest, Sara A. Gowdy, John M. Goyal, Manish Sheridan, Katherine C. Wasdahl, Daniel A. Radiol Case Rep Article A 51-year-old Caucasian female presenting with renal-cell cancer and cutaneous leiomyomas was later diagnosed with Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) Syndrome. HLRCC is an autosomal dominant condition caused by a mutation in the fumarate hydratase gene, which encodes for an enzyme in the citric acid cycle. This syndrome has been reported in over 100 families throughout the world, the majority of whom are of Eastern European descent. Those with this syndrome have a significantly increased risk of developing renal-cell carcinoma, cutaneous leiomyomas, and uterine leiomyomas, and a smaller chance of developing uterine leiomyosarcomas. This syndrome has a relatively poor prognosis, with tumor metastasis occurring in approximately 50% of patients. However, more aggressive prophylactic measures and recent studies have shown potential to improve patient prognosis. Elsevier 2015-12-03 /pmc/articles/PMC4921156/ /pubmed/27408652 http://dx.doi.org/10.2484/rcr.v10i1.962 Text en © 2015 The Authors. 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 Article
Fondriest, Sara A.
Gowdy, John M.
Goyal, Manish
Sheridan, Katherine C.
Wasdahl, Daniel A.
Concurrent renal-cell carcinoma and cutaneous leiomyomas: A case of HLRCC
title Concurrent renal-cell carcinoma and cutaneous leiomyomas: A case of HLRCC
title_full Concurrent renal-cell carcinoma and cutaneous leiomyomas: A case of HLRCC
title_fullStr Concurrent renal-cell carcinoma and cutaneous leiomyomas: A case of HLRCC
title_full_unstemmed Concurrent renal-cell carcinoma and cutaneous leiomyomas: A case of HLRCC
title_short Concurrent renal-cell carcinoma and cutaneous leiomyomas: A case of HLRCC
title_sort concurrent renal-cell carcinoma and cutaneous leiomyomas: a case of hlrcc
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921156/
https://www.ncbi.nlm.nih.gov/pubmed/27408652
http://dx.doi.org/10.2484/rcr.v10i1.962
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