Spontaneous pneumothorax as manifestation of Marfan syndrome
The authors describe a 16-year-old boy, previously healthy, who was admitted to our hospital for left-sided spontaneous pneumothorax. On physical examination he presented with marfanoid habitus. Pneumothorax was managed conservatively with resolution. Four months later he had a recurrence of left-si...
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Veröffentlicht in: | BMJ Case Reports 2013, Vol.2013 |
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creator | Viveiro, Carolina Rocha, Patricia Carvalho, Cristiana Zarcos, Maria Manuel |
description | The authors describe a 16-year-old boy, previously healthy, who was admitted to our hospital for left-sided spontaneous pneumothorax. On physical examination he presented with marfanoid habitus. Pneumothorax was managed conservatively with resolution. Four months later he had a recurrence of left-sided pneumothorax and 1 week after that he presented with contralateral pneumothorax. He underwent video-assisted thoracoscopic surgery twice for bullectomy and pleurodesis. No further recurrence was stated. Additional investigation showed a prolapsed cardiac mitral valve and Marfan syndrome was confirmed genetically. |
doi_str_mv | 10.1136/bcr-2013-201697 |
format | Report |
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On physical examination he presented with marfanoid habitus. Pneumothorax was managed conservatively with resolution. Four months later he had a recurrence of left-sided pneumothorax and 1 week after that he presented with contralateral pneumothorax. He underwent video-assisted thoracoscopic surgery twice for bullectomy and pleurodesis. No further recurrence was stated. Additional investigation showed a prolapsed cardiac mitral valve and Marfan syndrome was confirmed genetically.</description><identifier>EISSN: 1757-790X</identifier><identifier>DOI: 10.1136/bcr-2013-201697</identifier><language>eng</language><publisher>BMJ Publishing Group Ltd</publisher><ispartof>BMJ Case Reports, 2013, Vol.2013</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,780,4476,27902</link.rule.ids></links><search><creatorcontrib>Viveiro, Carolina</creatorcontrib><creatorcontrib>Rocha, Patricia</creatorcontrib><creatorcontrib>Carvalho, Cristiana</creatorcontrib><creatorcontrib>Zarcos, Maria Manuel</creatorcontrib><title>Spontaneous pneumothorax as manifestation of Marfan syndrome</title><title>BMJ Case Reports</title><addtitle>BMJ Case Reports</addtitle><description>The authors describe a 16-year-old boy, previously healthy, who was admitted to our hospital for left-sided spontaneous pneumothorax. On physical examination he presented with marfanoid habitus. Pneumothorax was managed conservatively with resolution. Four months later he had a recurrence of left-sided pneumothorax and 1 week after that he presented with contralateral pneumothorax. He underwent video-assisted thoracoscopic surgery twice for bullectomy and pleurodesis. No further recurrence was stated. 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On physical examination he presented with marfanoid habitus. Pneumothorax was managed conservatively with resolution. Four months later he had a recurrence of left-sided pneumothorax and 1 week after that he presented with contralateral pneumothorax. He underwent video-assisted thoracoscopic surgery twice for bullectomy and pleurodesis. No further recurrence was stated. Additional investigation showed a prolapsed cardiac mitral valve and Marfan syndrome was confirmed genetically.</abstract><pub>BMJ Publishing Group Ltd</pub><doi>10.1136/bcr-2013-201697</doi></addata></record> |
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source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
title | Spontaneous pneumothorax as manifestation of Marfan syndrome |
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