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Bilateral Renal Tumour as Indicator for Birt-Hogg-Dubé Syndrome

Birt-Hogg-Dubé (BHD) syndrome is a cancer disorder caused by a pathogenic FLCN mutation characterized by fibrofolliculomas, lung cysts, pneumothorax, benign renal cyst, and renal cell carcinoma (RCC). In this case we describe a patient with bilateral renal tumour and a positive familial history for...

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Autores principales: Johannesma, P. C., van Moorselaar, R. J. A., Horenblas, S., van der Kolk, L. E., Thunnissen, E., van Waesberghe, J. H. T. M., Menko, F. H., Postmus, P. E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3977462/
https://www.ncbi.nlm.nih.gov/pubmed/24772173
http://dx.doi.org/10.1155/2014/618675
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author Johannesma, P. C.
van Moorselaar, R. J. A.
Horenblas, S.
van der Kolk, L. E.
Thunnissen, E.
van Waesberghe, J. H. T. M.
Menko, F. H.
Postmus, P. E.
author_facet Johannesma, P. C.
van Moorselaar, R. J. A.
Horenblas, S.
van der Kolk, L. E.
Thunnissen, E.
van Waesberghe, J. H. T. M.
Menko, F. H.
Postmus, P. E.
author_sort Johannesma, P. C.
collection PubMed
description Birt-Hogg-Dubé (BHD) syndrome is a cancer disorder caused by a pathogenic FLCN mutation characterized by fibrofolliculomas, lung cysts, pneumothorax, benign renal cyst, and renal cell carcinoma (RCC). In this case we describe a patient with bilateral renal tumour and a positive familial history for pneumothorax and renal cancer. Based on this clinical presentation, the patient was suspected for BHD syndrome, which was confirmed after molecular testing. We discuss the importance of recognizing this autosomal dominant cancer disorder when a patient is presented at the urologist with a positive family history of chromophobe renal cell cancer or a positive familial history for renal cell cancer and pneumothorax.
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spelling pubmed-39774622014-04-27 Bilateral Renal Tumour as Indicator for Birt-Hogg-Dubé Syndrome Johannesma, P. C. van Moorselaar, R. J. A. Horenblas, S. van der Kolk, L. E. Thunnissen, E. van Waesberghe, J. H. T. M. Menko, F. H. Postmus, P. E. Case Rep Med Case Report Birt-Hogg-Dubé (BHD) syndrome is a cancer disorder caused by a pathogenic FLCN mutation characterized by fibrofolliculomas, lung cysts, pneumothorax, benign renal cyst, and renal cell carcinoma (RCC). In this case we describe a patient with bilateral renal tumour and a positive familial history for pneumothorax and renal cancer. Based on this clinical presentation, the patient was suspected for BHD syndrome, which was confirmed after molecular testing. We discuss the importance of recognizing this autosomal dominant cancer disorder when a patient is presented at the urologist with a positive family history of chromophobe renal cell cancer or a positive familial history for renal cell cancer and pneumothorax. Hindawi Publishing Corporation 2014 2014-03-20 /pmc/articles/PMC3977462/ /pubmed/24772173 http://dx.doi.org/10.1155/2014/618675 Text en Copyright © 2014 P. C. Johannesma et al. https://creativecommons.org/licenses/by/3.0/ 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
Johannesma, P. C.
van Moorselaar, R. J. A.
Horenblas, S.
van der Kolk, L. E.
Thunnissen, E.
van Waesberghe, J. H. T. M.
Menko, F. H.
Postmus, P. E.
Bilateral Renal Tumour as Indicator for Birt-Hogg-Dubé Syndrome
title Bilateral Renal Tumour as Indicator for Birt-Hogg-Dubé Syndrome
title_full Bilateral Renal Tumour as Indicator for Birt-Hogg-Dubé Syndrome
title_fullStr Bilateral Renal Tumour as Indicator for Birt-Hogg-Dubé Syndrome
title_full_unstemmed Bilateral Renal Tumour as Indicator for Birt-Hogg-Dubé Syndrome
title_short Bilateral Renal Tumour as Indicator for Birt-Hogg-Dubé Syndrome
title_sort bilateral renal tumour as indicator for birt-hogg-dubé syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3977462/
https://www.ncbi.nlm.nih.gov/pubmed/24772173
http://dx.doi.org/10.1155/2014/618675
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