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A Case of Hereditary Leiomyomatosis and Renal Cell Carcinoma

A 49-year-old lady presented with multiple recurring painful lesions over her thighs, arms, and back. Past medical history included a left sided nephrectomy for renal cell carcinoma and a hysterectomy for multiple uterine fibroids (leiomyomas). Histopathological examination revealed changes consiste...

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Detalles Bibliográficos
Autores principales: Mehrtens, Sarah, Veitch, David, Kulakov, Elizabeth, Perrett, Conal M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837255/
https://www.ncbi.nlm.nih.gov/pubmed/27144040
http://dx.doi.org/10.1155/2016/3793986
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author Mehrtens, Sarah
Veitch, David
Kulakov, Elizabeth
Perrett, Conal M.
author_facet Mehrtens, Sarah
Veitch, David
Kulakov, Elizabeth
Perrett, Conal M.
author_sort Mehrtens, Sarah
collection PubMed
description A 49-year-old lady presented with multiple recurring painful lesions over her thighs, arms, and back. Past medical history included a left sided nephrectomy for renal cell carcinoma and a hysterectomy for multiple uterine fibroids (leiomyomas). Histopathological examination revealed changes consistent with pilar leiomyomas. Gene mutation analysis confirmed a diagnosis of hereditary leiomyomatosis and renal cell carcinoma. Hereditary leiomyomatosis and renal cell carcinoma is an uncommon autosomal dominant condition characterised by the concurrent presentation of cutaneous and uterine leiomyomas. Renal cell carcinoma associated with this condition is more aggressive and a significant cause of mortality. Due to this association with potentially fatal renal cell carcinoma we felt that it was important to highlight this case with an update on pathophysiology and management.
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spelling pubmed-48372552016-05-03 A Case of Hereditary Leiomyomatosis and Renal Cell Carcinoma Mehrtens, Sarah Veitch, David Kulakov, Elizabeth Perrett, Conal M. Case Rep Dermatol Med Case Report A 49-year-old lady presented with multiple recurring painful lesions over her thighs, arms, and back. Past medical history included a left sided nephrectomy for renal cell carcinoma and a hysterectomy for multiple uterine fibroids (leiomyomas). Histopathological examination revealed changes consistent with pilar leiomyomas. Gene mutation analysis confirmed a diagnosis of hereditary leiomyomatosis and renal cell carcinoma. Hereditary leiomyomatosis and renal cell carcinoma is an uncommon autosomal dominant condition characterised by the concurrent presentation of cutaneous and uterine leiomyomas. Renal cell carcinoma associated with this condition is more aggressive and a significant cause of mortality. Due to this association with potentially fatal renal cell carcinoma we felt that it was important to highlight this case with an update on pathophysiology and management. Hindawi Publishing Corporation 2016 2016-04-07 /pmc/articles/PMC4837255/ /pubmed/27144040 http://dx.doi.org/10.1155/2016/3793986 Text en Copyright © 2016 Sarah Mehrtens et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mehrtens, Sarah
Veitch, David
Kulakov, Elizabeth
Perrett, Conal M.
A Case of Hereditary Leiomyomatosis and Renal Cell Carcinoma
title A Case of Hereditary Leiomyomatosis and Renal Cell Carcinoma
title_full A Case of Hereditary Leiomyomatosis and Renal Cell Carcinoma
title_fullStr A Case of Hereditary Leiomyomatosis and Renal Cell Carcinoma
title_full_unstemmed A Case of Hereditary Leiomyomatosis and Renal Cell Carcinoma
title_short A Case of Hereditary Leiomyomatosis and Renal Cell Carcinoma
title_sort case of hereditary leiomyomatosis and renal cell carcinoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837255/
https://www.ncbi.nlm.nih.gov/pubmed/27144040
http://dx.doi.org/10.1155/2016/3793986
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