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Childhood pneumothorax in Birt‐Hogg‐Dubé syndrome: A cohort study and review of the literature
BACKGROUND: Birt‐Hogg‐Dubé syndrome (BHD) is an autosomal dominantly inherited cancer predisposition syndrome associated with an increased risk of spontaneous pneumothorax (SP) and renal cell carcinoma in the adult population. Recent studies suggest that BHD accounts for up to 10% of all SP in adult...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014440/ https://www.ncbi.nlm.nih.gov/pubmed/29439288 http://dx.doi.org/10.1002/mgg3.373 |
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author | Geilswijk, Marianne Bendstrup, Elisabeth Madsen, Mia Gebauer Sommerlund, Mette Skytte, Anne‐Bine |
author_facet | Geilswijk, Marianne Bendstrup, Elisabeth Madsen, Mia Gebauer Sommerlund, Mette Skytte, Anne‐Bine |
author_sort | Geilswijk, Marianne |
collection | PubMed |
description | BACKGROUND: Birt‐Hogg‐Dubé syndrome (BHD) is an autosomal dominantly inherited cancer predisposition syndrome associated with an increased risk of spontaneous pneumothorax (SP) and renal cell carcinoma in the adult population. Recent studies suggest that BHD accounts for up to 10% of all SP in adults and BHD in children with SP have been reported. METHODS: To explore to what extent BHD is the cause of childhood pneumothorax, we studied a Danish BHD cohort consisting of 109 cases from 22 families. Clinical data was gathered by review of medical records. A systematic literature search concerning childhood and adolescence pneumothorax in BHD was performed and identified publications reviewed. RESULTS: In our cohort, three of 109 BHD cases experienced childhood pneumothorax, corresponding to a prevalence of 3%. Reviewing the literature, data regarding more than 800 BHD cases were covered. Only seven previously published cases of childhood pneumothorax in BHD were identified. CONCLUSION: Our findings suggest that BHD is likely the cause of a larger subset of childhood pneumothoraces than hitherto recognized. Awareness of BHD as a cause of childhood pneumothorax needs to be raised to provide patients and relatives with the possibility of specialized management of SP and regular renal cancer surveillance. |
format | Online Article Text |
id | pubmed-6014440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60144402018-07-05 Childhood pneumothorax in Birt‐Hogg‐Dubé syndrome: A cohort study and review of the literature Geilswijk, Marianne Bendstrup, Elisabeth Madsen, Mia Gebauer Sommerlund, Mette Skytte, Anne‐Bine Mol Genet Genomic Med Original Articles BACKGROUND: Birt‐Hogg‐Dubé syndrome (BHD) is an autosomal dominantly inherited cancer predisposition syndrome associated with an increased risk of spontaneous pneumothorax (SP) and renal cell carcinoma in the adult population. Recent studies suggest that BHD accounts for up to 10% of all SP in adults and BHD in children with SP have been reported. METHODS: To explore to what extent BHD is the cause of childhood pneumothorax, we studied a Danish BHD cohort consisting of 109 cases from 22 families. Clinical data was gathered by review of medical records. A systematic literature search concerning childhood and adolescence pneumothorax in BHD was performed and identified publications reviewed. RESULTS: In our cohort, three of 109 BHD cases experienced childhood pneumothorax, corresponding to a prevalence of 3%. Reviewing the literature, data regarding more than 800 BHD cases were covered. Only seven previously published cases of childhood pneumothorax in BHD were identified. CONCLUSION: Our findings suggest that BHD is likely the cause of a larger subset of childhood pneumothoraces than hitherto recognized. Awareness of BHD as a cause of childhood pneumothorax needs to be raised to provide patients and relatives with the possibility of specialized management of SP and regular renal cancer surveillance. John Wiley and Sons Inc. 2018-02-13 /pmc/articles/PMC6014440/ /pubmed/29439288 http://dx.doi.org/10.1002/mgg3.373 Text en © 2018 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Geilswijk, Marianne Bendstrup, Elisabeth Madsen, Mia Gebauer Sommerlund, Mette Skytte, Anne‐Bine Childhood pneumothorax in Birt‐Hogg‐Dubé syndrome: A cohort study and review of the literature |
title | Childhood pneumothorax in Birt‐Hogg‐Dubé syndrome: A cohort study and review of the literature |
title_full | Childhood pneumothorax in Birt‐Hogg‐Dubé syndrome: A cohort study and review of the literature |
title_fullStr | Childhood pneumothorax in Birt‐Hogg‐Dubé syndrome: A cohort study and review of the literature |
title_full_unstemmed | Childhood pneumothorax in Birt‐Hogg‐Dubé syndrome: A cohort study and review of the literature |
title_short | Childhood pneumothorax in Birt‐Hogg‐Dubé syndrome: A cohort study and review of the literature |
title_sort | childhood pneumothorax in birt‐hogg‐dubé syndrome: a cohort study and review of the literature |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014440/ https://www.ncbi.nlm.nih.gov/pubmed/29439288 http://dx.doi.org/10.1002/mgg3.373 |
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