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A case of recurrent pneumothorax and skin lesions diagnosed with Birt–Hogg–Dubé

Birt–Hogg–Dubé (BHD) syndrome is an autosomal dominant disease that is manifested as benign cutaneous tumors, multiple lung parenchymal cysts and an increased risk of renal cancer. Its symptoms usually do not appear until adulthood. We report a patient who was admitted with recurrent pneumothorax. D...

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Autores principales: Takaldani, Ali Hossein Samadi, Negaresh, Mohammad, Jalalzadeh, Solmaz, Lotfi, Leila, Ghobadi, Hassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127950/
https://www.ncbi.nlm.nih.gov/pubmed/35619682
http://dx.doi.org/10.1093/omcr/omac054
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author Takaldani, Ali Hossein Samadi
Negaresh, Mohammad
Jalalzadeh, Solmaz
Lotfi, Leila
Ghobadi, Hassan
author_facet Takaldani, Ali Hossein Samadi
Negaresh, Mohammad
Jalalzadeh, Solmaz
Lotfi, Leila
Ghobadi, Hassan
author_sort Takaldani, Ali Hossein Samadi
collection PubMed
description Birt–Hogg–Dubé (BHD) syndrome is an autosomal dominant disease that is manifested as benign cutaneous tumors, multiple lung parenchymal cysts and an increased risk of renal cancer. Its symptoms usually do not appear until adulthood. We report a patient who was admitted with recurrent pneumothorax. Discovering typical cutaneous lesions accompanied with a history of the same condition in his son, BHD syndrome was diagnosed.
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spelling pubmed-91279502022-05-25 A case of recurrent pneumothorax and skin lesions diagnosed with Birt–Hogg–Dubé Takaldani, Ali Hossein Samadi Negaresh, Mohammad Jalalzadeh, Solmaz Lotfi, Leila Ghobadi, Hassan Oxf Med Case Reports Case Report Birt–Hogg–Dubé (BHD) syndrome is an autosomal dominant disease that is manifested as benign cutaneous tumors, multiple lung parenchymal cysts and an increased risk of renal cancer. Its symptoms usually do not appear until adulthood. We report a patient who was admitted with recurrent pneumothorax. Discovering typical cutaneous lesions accompanied with a history of the same condition in his son, BHD syndrome was diagnosed. Oxford University Press 2022-05-23 /pmc/articles/PMC9127950/ /pubmed/35619682 http://dx.doi.org/10.1093/omcr/omac054 Text en © The Author(s) 2022. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Takaldani, Ali Hossein Samadi
Negaresh, Mohammad
Jalalzadeh, Solmaz
Lotfi, Leila
Ghobadi, Hassan
A case of recurrent pneumothorax and skin lesions diagnosed with Birt–Hogg–Dubé
title A case of recurrent pneumothorax and skin lesions diagnosed with Birt–Hogg–Dubé
title_full A case of recurrent pneumothorax and skin lesions diagnosed with Birt–Hogg–Dubé
title_fullStr A case of recurrent pneumothorax and skin lesions diagnosed with Birt–Hogg–Dubé
title_full_unstemmed A case of recurrent pneumothorax and skin lesions diagnosed with Birt–Hogg–Dubé
title_short A case of recurrent pneumothorax and skin lesions diagnosed with Birt–Hogg–Dubé
title_sort case of recurrent pneumothorax and skin lesions diagnosed with birt–hogg–dubé
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127950/
https://www.ncbi.nlm.nih.gov/pubmed/35619682
http://dx.doi.org/10.1093/omcr/omac054
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