Congenital cystic adenomatoid malformation of lung type 1
Abstract Congenital cystic adenomatoid malformation, a rare developmental, hamartomatous abnormality of the lung, usually is unilateral, is localized, and presents in early infancy. Delayed occurrence in older children and multilobar involvement are rare. We describe a case of congenital cystic aden...
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Veröffentlicht in: | Journal of pediatric surgery 2010-02, Vol.45 (2), p.e25-e28 |
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creator | Mathai, Alka Mary Kini, Hema Pai, Muktha R Shetty, Ashok B Murali, Nirupama |
description | Abstract Congenital cystic adenomatoid malformation, a rare developmental, hamartomatous abnormality of the lung, usually is unilateral, is localized, and presents in early infancy. Delayed occurrence in older children and multilobar involvement are rare. We describe a case of congenital cystic adenomatoid malformation type 1 with multilobar involvement, associated emphysema, and coexistent tracheobronchopathia osteochondroplastica in an adolescent girl for whom the correct diagnosis was achieved only on histologic examination. The importance of an accurate diagnosis of this entity enables proper subtyping, management to minimize the risk of infections and malignancy, and exclusion of associated malformations. |
doi_str_mv | 10.1016/j.jpedsurg.2009.11.022 |
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Delayed occurrence in older children and multilobar involvement are rare. We describe a case of congenital cystic adenomatoid malformation type 1 with multilobar involvement, associated emphysema, and coexistent tracheobronchopathia osteochondroplastica in an adolescent girl for whom the correct diagnosis was achieved only on histologic examination. The importance of an accurate diagnosis of this entity enables proper subtyping, management to minimize the risk of infections and malignancy, and exclusion of associated malformations.</description><identifier>ISSN: 0022-3468</identifier><identifier>EISSN: 1531-5037</identifier><identifier>DOI: 10.1016/j.jpedsurg.2009.11.022</identifier><identifier>PMID: 20152335</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Abnormalities, Multiple - diagnosis ; Abnormalities, Multiple - epidemiology ; Abnormalities, Multiple - pathology ; Adolescent ; CCAM type 1 ; Comorbidity ; Cystic Adenomatoid Malformation of Lung, Congenital - diagnosis ; Cystic Adenomatoid Malformation of Lung, Congenital - epidemiology ; Cystic Adenomatoid Malformation of Lung, Congenital - pathology ; Diagnosis, Differential ; Emphysema ; Female ; Functional Laterality ; Humans ; Lung ; Lung - pathology ; Lung - surgery ; Multilobar ; Pediatrics ; Pneumonectomy ; Pulmonary Emphysema - epidemiology ; Pulmonary Emphysema - pathology ; Surgery ; Tracheobronchomalacia - diagnosis ; Tracheobronchomalacia - epidemiology ; Tracheobronchomalacia - pathology ; Tracheobronchopathia osteochondroplastica</subject><ispartof>Journal of pediatric surgery, 2010-02, Vol.45 (2), p.e25-e28</ispartof><rights>Elsevier Inc.</rights><rights>2010 Elsevier Inc.</rights><rights>Copyright 2010 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-150aa238bf053bf67a7bda482c7f0fcb65a4cc15b70efddc2b8dc66f25561a6a3</citedby><cites>FETCH-LOGICAL-c422t-150aa238bf053bf67a7bda482c7f0fcb65a4cc15b70efddc2b8dc66f25561a6a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jpedsurg.2009.11.022$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20152335$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mathai, Alka Mary</creatorcontrib><creatorcontrib>Kini, Hema</creatorcontrib><creatorcontrib>Pai, Muktha R</creatorcontrib><creatorcontrib>Shetty, Ashok B</creatorcontrib><creatorcontrib>Murali, Nirupama</creatorcontrib><title>Congenital cystic adenomatoid malformation of lung type 1</title><title>Journal of pediatric surgery</title><addtitle>J Pediatr Surg</addtitle><description>Abstract Congenital cystic adenomatoid malformation, a rare developmental, hamartomatous abnormality of the lung, usually is unilateral, is localized, and presents in early infancy. Delayed occurrence in older children and multilobar involvement are rare. We describe a case of congenital cystic adenomatoid malformation type 1 with multilobar involvement, associated emphysema, and coexistent tracheobronchopathia osteochondroplastica in an adolescent girl for whom the correct diagnosis was achieved only on histologic examination. The importance of an accurate diagnosis of this entity enables proper subtyping, management to minimize the risk of infections and malignancy, and exclusion of associated malformations.</description><subject>Abnormalities, Multiple - diagnosis</subject><subject>Abnormalities, Multiple - epidemiology</subject><subject>Abnormalities, Multiple - pathology</subject><subject>Adolescent</subject><subject>CCAM type 1</subject><subject>Comorbidity</subject><subject>Cystic Adenomatoid Malformation of Lung, Congenital - diagnosis</subject><subject>Cystic Adenomatoid Malformation of Lung, Congenital - epidemiology</subject><subject>Cystic Adenomatoid Malformation of Lung, Congenital - pathology</subject><subject>Diagnosis, Differential</subject><subject>Emphysema</subject><subject>Female</subject><subject>Functional Laterality</subject><subject>Humans</subject><subject>Lung</subject><subject>Lung - pathology</subject><subject>Lung - surgery</subject><subject>Multilobar</subject><subject>Pediatrics</subject><subject>Pneumonectomy</subject><subject>Pulmonary Emphysema - epidemiology</subject><subject>Pulmonary Emphysema - pathology</subject><subject>Surgery</subject><subject>Tracheobronchomalacia - diagnosis</subject><subject>Tracheobronchomalacia - epidemiology</subject><subject>Tracheobronchomalacia - pathology</subject><subject>Tracheobronchopathia osteochondroplastica</subject><issn>0022-3468</issn><issn>1531-5037</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9r3DAQxUVJaTbbfoXgW052RtJK9l5Ky9I_gUAOac9ClkaLXFvaSnZgv321bJJDLzkNM7x5w_sNIdcUGgpU3g7NcECbl7RvGMC2obQBxt6RFRWc1gJ4e0FWUEY138juklzlPACUMdAP5JIBFYxzsSLbXQx7DH7WY2WOefam0hZDnPQcva0mPbqYSuNjqKKrxiXsq_l4wIp-JO-dHjN-eq5r8vv7t1-7n_X9w4-73df72mwYm2sqQGvGu96B4L2TrW57qzcdM60DZ3op9MYYKvoW0FlrWN9ZI6VjQkiqpeZrcnP2PaT4d8E8q8lng-OoA8Ylq5bzLXBecq-JPCtNijkndOqQ_KTTUVFQJ2pqUC_U1ImaolQVRGXx-vnE0k9oX9deMBXBl7MAS9Anj0ll4zEYtD6hmZWN_u0bn_-zMKMP3ujxDx4xD3FJoWBUVGWmQD2efnd6HWyLSScF_wc-opac</recordid><startdate>20100201</startdate><enddate>20100201</enddate><creator>Mathai, Alka Mary</creator><creator>Kini, Hema</creator><creator>Pai, Muktha R</creator><creator>Shetty, Ashok B</creator><creator>Murali, Nirupama</creator><general>Elsevier Inc</general><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>20100201</creationdate><title>Congenital cystic adenomatoid malformation of lung type 1</title><author>Mathai, Alka Mary ; Kini, Hema ; Pai, Muktha R ; Shetty, Ashok B ; Murali, Nirupama</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-150aa238bf053bf67a7bda482c7f0fcb65a4cc15b70efddc2b8dc66f25561a6a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Abnormalities, Multiple - diagnosis</topic><topic>Abnormalities, Multiple - epidemiology</topic><topic>Abnormalities, Multiple - pathology</topic><topic>Adolescent</topic><topic>CCAM type 1</topic><topic>Comorbidity</topic><topic>Cystic Adenomatoid Malformation of Lung, Congenital - diagnosis</topic><topic>Cystic Adenomatoid Malformation of Lung, Congenital - epidemiology</topic><topic>Cystic Adenomatoid Malformation of Lung, Congenital - pathology</topic><topic>Diagnosis, Differential</topic><topic>Emphysema</topic><topic>Female</topic><topic>Functional Laterality</topic><topic>Humans</topic><topic>Lung</topic><topic>Lung - pathology</topic><topic>Lung - surgery</topic><topic>Multilobar</topic><topic>Pediatrics</topic><topic>Pneumonectomy</topic><topic>Pulmonary Emphysema - epidemiology</topic><topic>Pulmonary Emphysema - pathology</topic><topic>Surgery</topic><topic>Tracheobronchomalacia - diagnosis</topic><topic>Tracheobronchomalacia - epidemiology</topic><topic>Tracheobronchomalacia - pathology</topic><topic>Tracheobronchopathia osteochondroplastica</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mathai, Alka Mary</creatorcontrib><creatorcontrib>Kini, Hema</creatorcontrib><creatorcontrib>Pai, Muktha R</creatorcontrib><creatorcontrib>Shetty, Ashok B</creatorcontrib><creatorcontrib>Murali, Nirupama</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pediatric surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mathai, Alka Mary</au><au>Kini, Hema</au><au>Pai, Muktha R</au><au>Shetty, Ashok B</au><au>Murali, Nirupama</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Congenital cystic adenomatoid malformation of lung type 1</atitle><jtitle>Journal of pediatric surgery</jtitle><addtitle>J Pediatr Surg</addtitle><date>2010-02-01</date><risdate>2010</risdate><volume>45</volume><issue>2</issue><spage>e25</spage><epage>e28</epage><pages>e25-e28</pages><issn>0022-3468</issn><eissn>1531-5037</eissn><abstract>Abstract Congenital cystic adenomatoid malformation, a rare developmental, hamartomatous abnormality of the lung, usually is unilateral, is localized, and presents in early infancy. Delayed occurrence in older children and multilobar involvement are rare. We describe a case of congenital cystic adenomatoid malformation type 1 with multilobar involvement, associated emphysema, and coexistent tracheobronchopathia osteochondroplastica in an adolescent girl for whom the correct diagnosis was achieved only on histologic examination. The importance of an accurate diagnosis of this entity enables proper subtyping, management to minimize the risk of infections and malignancy, and exclusion of associated malformations.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>20152335</pmid><doi>10.1016/j.jpedsurg.2009.11.022</doi></addata></record> |
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subjects | Abnormalities, Multiple - diagnosis Abnormalities, Multiple - epidemiology Abnormalities, Multiple - pathology Adolescent CCAM type 1 Comorbidity Cystic Adenomatoid Malformation of Lung, Congenital - diagnosis Cystic Adenomatoid Malformation of Lung, Congenital - epidemiology Cystic Adenomatoid Malformation of Lung, Congenital - pathology Diagnosis, Differential Emphysema Female Functional Laterality Humans Lung Lung - pathology Lung - surgery Multilobar Pediatrics Pneumonectomy Pulmonary Emphysema - epidemiology Pulmonary Emphysema - pathology Surgery Tracheobronchomalacia - diagnosis Tracheobronchomalacia - epidemiology Tracheobronchomalacia - pathology Tracheobronchopathia osteochondroplastica |
title | Congenital cystic adenomatoid malformation of lung type 1 |
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