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      Recommendations on scuba diving in Birt-Hogg-Dubé syndrome

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          ABSTRACT

          Introduction

          Although very uncommon, severe injury and death can occur during scuba diving. One of the main causes of scuba diving fatalities is pulmonary barotrauma due to significant changes in ambient pressure. Pathology of the lung parenchyma, such as cystic lesions, might increase the risk of pulmonary barotrauma.

          Areas covered

          Birt–Hogg–Dubé syndrome (BHD), caused by pathogenic variants in the FLCN gene, is characterized by skin fibrofolliculomas, an increased risk of renal cell carcinoma, multiple lung cysts and spontaneous pneumothorax. Given the pulmonary involvement, in some countries patients with BHD are generally recommended to avoid scuba diving, although evidence-based guidelines are lacking. We aim to provide recommendations on scuba diving for patients with BHD, based on a survey of literature on pulmonary cysts and pulmonary barotrauma in scuba diving.

          Expert opinion

          In our opinion, although the absolute risks are likely to be low, caution is warranted. Given the relative paucity of literature and the potential fatal outcome, patients with BHD with a strong desire for scuba diving should be informed of the potential risks in a personal assessment. If available a diving physician should be consulted, and a low radiation dose chest computed tomography (CT)-scan to assess pulmonary lesions could be considered.

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          Most cited references43

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          Birt-Hogg-Dubé syndrome: diagnosis and management.

          Birt-Hogg-Dubé syndrome (BHD) is an autosomal dominant condition characterised clinically by skin fibrofolliculomas, pulmonary cysts, spontaneous pneumothorax, and renal cancer. The condition is caused by germline mutations in the FLCN gene, which encodes folliculin; the function of this protein is largely unknown, although FLCN has been linked to the mTOR pathway. The availability of DNA-based diagnosis has allowed insight into the great variation in expression of FLCN, both within and between families. Patients can present with skin signs and also with pneumothorax or renal cancer. Preventive measures are aimed mainly at early diagnosis and treatment of renal cancer. This Review gives an overview of current diagnosis and management of BHD.
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            Lung cysts, spontaneous pneumothorax, and genetic associations in 89 families with Birt-Hogg-Dubé syndrome.

            Birt-Hogg-Dubé syndrome (BHDS) is an autosomal, dominantly inherited genodermatosis that predisposes to fibrofolliculomas, kidney neoplasms, lung cysts, and spontaneous pneumothorax. We evaluated 198 patients from 89 families with BHDS to characterize the risk factors for pneumothorax and genotype-pulmonary associations. Helical computed tomography scans of the chest were used to screen for pulmonary abnormalities. BHD mutation data were used for genotype-pulmonary associations. We examined the relationship of pneumothorax with categorical parameters (sex, smoking history, and lung cysts) and continuous parameters (number of cysts, lung cyst volume, and largest cyst diameter and volume). Logistic regression analyses were used to identify the risk factors associated with pneumothorax. Twenty-four percent (48/198) of patients with BHDS had a history of pneumothorax. The presence of lung cysts was significantly associated with pneumothorax (p = 0.006). Total lung cyst volume, largest cyst diameter and volume, and every parameter related to the number of lung cysts were significantly associated (p < 0.0001) with pneumothorax. A logistic regression analysis showed that only the total number of cysts in the right parenchymal lower lobe and the total number of cysts located on the pleural surface in the right middle lobe were needed to classify a patient as to whether or not he or she was likely to have a pneumothorax. Exon location of the BHD mutation was associated with the numbers of cysts (p = 0.0002). This study indicates that patients with BHDS have a significant association between lung cysts and spontaneous pneumothorax.
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              Decompression illness.

              Decompression illness is caused by intravascular or extravascular bubbles that are formed as a result of reduction in environmental pressure (decompression). The term covers both arterial gas embolism, in which alveolar gas or venous gas emboli (via cardiac shunts or via pulmonary vessels) are introduced into the arterial circulation, and decompression sickness, which is caused by in-situ bubble formation from dissolved inert gas. Both syndromes can occur in divers, compressed air workers, aviators, and astronauts, but arterial gas embolism also arises from iatrogenic causes unrelated to decompression. Risk of decompression illness is affected by immersion, exercise, and heat or cold. Manifestations range from itching and minor pain to neurological symptoms, cardiac collapse, and death. First-aid treatment is 100% oxygen and definitive treatment is recompression to increased pressure, breathing 100% oxygen. Adjunctive treatment, including fluid administration and prophylaxis against venous thromboembolism in paralysed patients, is also recommended. Treatment is, in most cases, effective although residual deficits can remain in serious cases, even after several recompressions. Copyright © 2011 Elsevier Ltd. All rights reserved.
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                Author and article information

                Journal
                Expert Rev Respir Med
                Expert Rev Respir Med
                Expert Review of Respiratory Medicine
                Taylor & Francis
                1747-6348
                1747-6356
                26 December 2023
                2023
                26 December 2023
                : 17
                : 11
                : 1003-1008
                Affiliations
                [a ]Department of Human Genetics, Amsterdam UMC, University of Amsterdam; , Amsterdam, Netherlands
                [b ]Department of Human Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Cancer Center Amsterdam; , Amsterdam, Netherlands
                [c ]Department of Hyperbaric Medicine, Amsterdam UMC, University of Amsterdam; , Amsterdam, Netherlands
                [d ]Department of Urology, Amsterdam UMC, Vrije Universiteit Amsterdam; , Amsterdam, Netherlands
                [e ]Department of Pulmonary Medicine, Amsterdam UMC, Vrije Universiteit Amsterdam; , Amsterdam, Netherlands
                [f ]Department of Dermatology, Amsterdam UMC, University of Amsterdam; , Amsterdam, Netherlands
                [g ]Department of Pathology, Erasmus MC, University Medical Center Rotterdam; , Rotterdam, Netherlands
                [h ]Cambridge Institute for Medical Research, Cambridge Biomedical Campus, University of Cambridge; , Cambridge, UK
                [i ]Royal Papworth Hospital; , Trumpington, Cambridge, UK
                [j ]Division of Pulmonary, Critical Care and Sleep Medicine, University of Cincinnati; , Cincinnati, Ohio, USA
                [k ]Family Cancer Clinic, Netherlands Cancer Institute; , Amsterdam, Netherlands
                Author notes
                CONTACT L. van Riel l.vanriel@ 123456amsterdamumc.nl Department of Human Genetics, University of Amsterdam; , Meibergdreef 9, Amsterdam, Netherlands
                AC. Houweling a.houweling@ 123456amsterdamumc.nl Department of Human Genetics,University of Amsterdam; , Meibergdreef 9, Amsterdam, Netherlands
                Author information
                https://orcid.org/0000-0003-1190-9925
                Article
                2284375
                10.1080/17476348.2023.2284375
                10763569
                37991821
                1b422f7c-b436-47d0-a086-cef3af1d3faa
                © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License ( http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.

                History
                Page count
                Figures: 1, Tables: 1, References: 45, Pages: 6
                Categories
                Review Article
                Review

                scuba diving,spontaneous pneumothorax,barotrauma,arterial gas embolism,lung cysts,birt–hogg–dubé syndrome,folliculin,flcn

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