Multiple pulmonary chondrohamartomas in trachea, bronchi and lung parenchyma. Review of the literature
Multiple pulmonary chondromatous hamartomas (MPCH) are rare, and MPCH with tracheal involvement have not been, to the best of our knowledge, reported before. Furthermore, there is no agreement in the literature about the origin of these tumours. We report a case of MPCH involving trachea, bronchi an...
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Veröffentlicht in: | Respiratory medicine 1996-02, Vol.90 (2), p.111-114 |
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description | Multiple pulmonary chondromatous hamartomas (MPCH) are rare, and MPCH with tracheal involvement have not been, to the best of our knowledge, reported before. Furthermore, there is no agreement in the literature about the origin of these tumours. We report a case of MPCH involving trachea, bronchi and lung parenchyma, incidentally found at the autopsy of a 88-year-old woman who died of acute myocardial infarction, and we review the literature about MPCH. We conclude that there appear to be two different types of multiple pulmonary chondromatous hamartomas; those presented in young patients often linked to gastric leiomyoblastomas and catecholamine-producing paragangliomas (Carney syndrome) with high mortality, and those presented in elderly patients, which seems to be compatible with life. |
doi_str_mv | 10.1016/S0954-6111(96)90208-5 |
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We conclude that there appear to be two different types of multiple pulmonary chondromatous hamartomas; those presented in young patients often linked to gastric leiomyoblastomas and catecholamine-producing paragangliomas (Carney syndrome) with high mortality, and those presented in elderly patients, which seems to be compatible with life.</description><identifier>ISSN: 0954-6111</identifier><identifier>EISSN: 1532-3064</identifier><identifier>DOI: 10.1016/S0954-6111(96)90208-5</identifier><identifier>PMID: 8730331</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Aged ; Aged, 80 and over ; Biological and medical sciences ; Bronchi - abnormalities ; Female ; Hamartoma - pathology ; Humans ; Lung - pathology ; Medical sciences ; Pneumology ; Trachea - abnormalities ; Tumors of the respiratory system and mediastinum</subject><ispartof>Respiratory medicine, 1996-02, Vol.90 (2), p.111-114</ispartof><rights>1996</rights><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-da2f363d7212e47ceffc9b2b9ed603eec6d8b4797c22bc20d2565c654cb322773</citedby><cites>FETCH-LOGICAL-c436t-da2f363d7212e47ceffc9b2b9ed603eec6d8b4797c22bc20d2565c654cb322773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0954611196902085$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3032812$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8730331$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Domínguez, H.</creatorcontrib><creatorcontrib>Hariri, J.</creatorcontrib><creatorcontrib>Pless, S.</creatorcontrib><title>Multiple pulmonary chondrohamartomas in trachea, bronchi and lung parenchyma. 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We conclude that there appear to be two different types of multiple pulmonary chondromatous hamartomas; those presented in young patients often linked to gastric leiomyoblastomas and catecholamine-producing paragangliomas (Carney syndrome) with high mortality, and those presented in elderly patients, which seems to be compatible with life.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Bronchi - abnormalities</subject><subject>Female</subject><subject>Hamartoma - pathology</subject><subject>Humans</subject><subject>Lung - pathology</subject><subject>Medical sciences</subject><subject>Pneumology</subject><subject>Trachea - abnormalities</subject><subject>Tumors of the respiratory system and mediastinum</subject><issn>0954-6111</issn><issn>1532-3064</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkFuL1DAUgIMo67j6ExbyIKJg11zatH1aZPEGK4KX55CenNpI2tQkVebfm9kZ5tWnA-d85_YRcsXZNWdcvfnG-qauFOf8Za9e9UywrmoekB1vpKgkU_VDsjsjj8mTlH4xxvq6Zhfkomslk5LvyPh589mtHum6-TksJu4pTGGxMUxmNjGH2STqFpqjgQnNazrEsMDkqFks9dvyk64mYsnsZ3NNv-Ifh39pGGmekHqXMZq8RXxKHo3GJ3x2ipfkx_t3328_VndfPny6fXtXQS1VrqwRo1TStoILrFvAcYR-EEOPVjGJCMp2Q932LQgxgGBWNKoB1dQwSCHaVl6SF8e5awy_N0xZzy4Bem8WDFvSbcdV8XEAmyMIMaQUcdRrdOXfveZMH_zqe7_6IE_3St_71U3puzot2IYZ7bnrJLTUn5_qJoHxYzQLuHTGCiQ6Lgp2c8SwyCjKok7gikW0LiJkbYP7zyH_ABBSmIQ</recordid><startdate>19960201</startdate><enddate>19960201</enddate><creator>Domínguez, H.</creator><creator>Hariri, J.</creator><creator>Pless, S.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19960201</creationdate><title>Multiple pulmonary chondrohamartomas in trachea, bronchi and lung parenchyma. 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Review of the literature</atitle><jtitle>Respiratory medicine</jtitle><addtitle>Respir Med</addtitle><date>1996-02-01</date><risdate>1996</risdate><volume>90</volume><issue>2</issue><spage>111</spage><epage>114</epage><pages>111-114</pages><issn>0954-6111</issn><eissn>1532-3064</eissn><abstract>Multiple pulmonary chondromatous hamartomas (MPCH) are rare, and MPCH with tracheal involvement have not been, to the best of our knowledge, reported before. Furthermore, there is no agreement in the literature about the origin of these tumours. We report a case of MPCH involving trachea, bronchi and lung parenchyma, incidentally found at the autopsy of a 88-year-old woman who died of acute myocardial infarction, and we review the literature about MPCH. We conclude that there appear to be two different types of multiple pulmonary chondromatous hamartomas; those presented in young patients often linked to gastric leiomyoblastomas and catecholamine-producing paragangliomas (Carney syndrome) with high mortality, and those presented in elderly patients, which seems to be compatible with life.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>8730331</pmid><doi>10.1016/S0954-6111(96)90208-5</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aged, 80 and over Biological and medical sciences Bronchi - abnormalities Female Hamartoma - pathology Humans Lung - pathology Medical sciences Pneumology Trachea - abnormalities Tumors of the respiratory system and mediastinum |
title | Multiple pulmonary chondrohamartomas in trachea, bronchi and lung parenchyma. Review of the literature |
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