Congenital pulmonary airway malformation: A case report of a rare cause of neonatal respiratory distress and review of the literature
Congenital pulmonary airway malformation (CPAM), formerly known as congenital cystic adenomatoid malformation (CCAM), is a rare developmental dysplastic lesion of the fetal tracheobronchial tree. CPAM is a rare cause of neonatal respiratory distress; however, its presence may span fetal to adult per...
Gespeichert in:
| Veröffentlicht in: | Nigerian journal of clinical practice 2019-11, Vol.22 (11), p.1621-1625 |
|---|---|
| Hauptverfasser: | , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 1625 |
|---|---|
| container_issue | 11 |
| container_start_page | 1621 |
| container_title | Nigerian journal of clinical practice |
| container_volume | 22 |
| creator | Disu, E Kehinde, O Anga, A Ubuane, P Itiola, A Akinola, I Falase, B |
| description | Congenital pulmonary airway malformation (CPAM), formerly known as congenital cystic adenomatoid malformation (CCAM), is a rare developmental dysplastic lesion of the fetal tracheobronchial tree. CPAM is a rare cause of neonatal respiratory distress; however, its presence may span fetal to adult period. In two previous case-reports from Nigeria, CPAM was present in post-neonatal infants. We report the case of a neonate, who presented with increasing respiratory distress and an abnormal chest radiograph, initially assumed as pneumonic changes. A revised diagnosis of CPAM was made after a chest computed tomography (CT) scan. The neonate subsequently had a successful excision of the affected lobe with remarkable clinical improvement. The case highlights the need to utilize superior imaging studies such as CT when plain radiographs are inconclusive. |
| doi_str_mv | 10.4103/njcp.njcp_20_19 |
| format | Article |
| fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2314252960</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A605798435</galeid><sourcerecordid>A605798435</sourcerecordid><originalsourceid>FETCH-LOGICAL-c454t-ad7c60c2d5d85351443aa035d45cabb4ddec6dc15bca5ee69c6e6f8e75ea04a93</originalsourceid><addsrcrecordid>eNp1kl9vFCEUxedBY2v12TdDYmJ82S0MMLPj27rxX9LEF30md-FOl5aBEZhO-gH83jJuqzbRkEDu5XdOgENVvWB0LRjl5_5Kj-tlUjVVrHtUnTLGuhWnbXtSPU3pitKm4xv2pDrhrGVdvWlPqx-74C_R2wyOjJMbgod4S8DGGW7JAK4PcYBsg39LtkRDQhJxDDGT0BMgESKW7lTapfZY1ItRxDTaCDkUK2NTLnUi4E3ZuLE4L2w-IHE2Y6GmiM-qxz24hM_v1rPq24f3X3efVhdfPn7ebS9WWkiRV2Ba3VBdG2k2kksmBAegXBohNez3whjUjdFM7jVIxKbTDTb9BluJQAV0_Kx6c_QdY_g-YcpqsEmjc1DOPiVVcyZqWXcNLeirI3oJDpX1fcgR9IKrbUNl220El4Va_4Mqw-BgdfDY29J_IHj9l-CA4PIhBTctT5wegudHUMeQUsRejdEOJRzFqFryVr-i_pN3Uby8u9y0H9D85u_DLsC7IzAHV14-XbtpxqgKe-3D_D9fxZqaqftvwn8C4PzD3w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2314252960</pqid></control><display><type>article</type><title>Congenital pulmonary airway malformation: A case report of a rare cause of neonatal respiratory distress and review of the literature</title><source>MEDLINE</source><source>African Journals Online (Open Access)</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Disu, E ; Kehinde, O ; Anga, A ; Ubuane, P ; Itiola, A ; Akinola, I ; Falase, B</creator><creatorcontrib>Disu, E ; Kehinde, O ; Anga, A ; Ubuane, P ; Itiola, A ; Akinola, I ; Falase, B</creatorcontrib><description>Congenital pulmonary airway malformation (CPAM), formerly known as congenital cystic adenomatoid malformation (CCAM), is a rare developmental dysplastic lesion of the fetal tracheobronchial tree. CPAM is a rare cause of neonatal respiratory distress; however, its presence may span fetal to adult period. In two previous case-reports from Nigeria, CPAM was present in post-neonatal infants. We report the case of a neonate, who presented with increasing respiratory distress and an abnormal chest radiograph, initially assumed as pneumonic changes. A revised diagnosis of CPAM was made after a chest computed tomography (CT) scan. The neonate subsequently had a successful excision of the affected lobe with remarkable clinical improvement. The case highlights the need to utilize superior imaging studies such as CT when plain radiographs are inconclusive.</description><identifier>ISSN: 1119-3077</identifier><identifier>DOI: 10.4103/njcp.njcp_20_19</identifier><identifier>PMID: 31719287</identifier><language>eng</language><publisher>India: Wolters Kluwer India Pvt. Ltd</publisher><subject>Chest x-rays ; Cystic Adenomatoid Malformation of Lung, Congenital - diagnosis ; Cystic Adenomatoid Malformation of Lung, Congenital - diagnostic imaging ; Cystic Adenomatoid Malformation of Lung, Congenital - surgery ; Female ; Genetic disorders ; Humans ; Infant, Newborn ; Infants ; Lung - diagnostic imaging ; Lung - pathology ; Male ; Newborn infants ; Nigeria ; Rare Diseases ; Respiratory Distress Syndrome, Newborn - etiology ; Respiratory Insufficiency ; Tomography, X-Ray Computed - methods</subject><ispartof>Nigerian journal of clinical practice, 2019-11, Vol.22 (11), p.1621-1625</ispartof><rights>COPYRIGHT 2019 Medknow Publications and Media Pvt. Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-ad7c60c2d5d85351443aa035d45cabb4ddec6dc15bca5ee69c6e6f8e75ea04a93</citedby><cites>FETCH-LOGICAL-c454t-ad7c60c2d5d85351443aa035d45cabb4ddec6dc15bca5ee69c6e6f8e75ea04a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27933,27934</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31719287$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Disu, E</creatorcontrib><creatorcontrib>Kehinde, O</creatorcontrib><creatorcontrib>Anga, A</creatorcontrib><creatorcontrib>Ubuane, P</creatorcontrib><creatorcontrib>Itiola, A</creatorcontrib><creatorcontrib>Akinola, I</creatorcontrib><creatorcontrib>Falase, B</creatorcontrib><title>Congenital pulmonary airway malformation: A case report of a rare cause of neonatal respiratory distress and review of the literature</title><title>Nigerian journal of clinical practice</title><addtitle>Niger J Clin Pract</addtitle><description>Congenital pulmonary airway malformation (CPAM), formerly known as congenital cystic adenomatoid malformation (CCAM), is a rare developmental dysplastic lesion of the fetal tracheobronchial tree. CPAM is a rare cause of neonatal respiratory distress; however, its presence may span fetal to adult period. In two previous case-reports from Nigeria, CPAM was present in post-neonatal infants. We report the case of a neonate, who presented with increasing respiratory distress and an abnormal chest radiograph, initially assumed as pneumonic changes. A revised diagnosis of CPAM was made after a chest computed tomography (CT) scan. The neonate subsequently had a successful excision of the affected lobe with remarkable clinical improvement. The case highlights the need to utilize superior imaging studies such as CT when plain radiographs are inconclusive.</description><subject>Chest x-rays</subject><subject>Cystic Adenomatoid Malformation of Lung, Congenital - diagnosis</subject><subject>Cystic Adenomatoid Malformation of Lung, Congenital - diagnostic imaging</subject><subject>Cystic Adenomatoid Malformation of Lung, Congenital - surgery</subject><subject>Female</subject><subject>Genetic disorders</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Infants</subject><subject>Lung - diagnostic imaging</subject><subject>Lung - pathology</subject><subject>Male</subject><subject>Newborn infants</subject><subject>Nigeria</subject><subject>Rare Diseases</subject><subject>Respiratory Distress Syndrome, Newborn - etiology</subject><subject>Respiratory Insufficiency</subject><subject>Tomography, X-Ray Computed - methods</subject><issn>1119-3077</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kl9vFCEUxedBY2v12TdDYmJ82S0MMLPj27rxX9LEF30md-FOl5aBEZhO-gH83jJuqzbRkEDu5XdOgENVvWB0LRjl5_5Kj-tlUjVVrHtUnTLGuhWnbXtSPU3pitKm4xv2pDrhrGVdvWlPqx-74C_R2wyOjJMbgod4S8DGGW7JAK4PcYBsg39LtkRDQhJxDDGT0BMgESKW7lTapfZY1ItRxDTaCDkUK2NTLnUi4E3ZuLE4L2w-IHE2Y6GmiM-qxz24hM_v1rPq24f3X3efVhdfPn7ebS9WWkiRV2Ba3VBdG2k2kksmBAegXBohNez3whjUjdFM7jVIxKbTDTb9BluJQAV0_Kx6c_QdY_g-YcpqsEmjc1DOPiVVcyZqWXcNLeirI3oJDpX1fcgR9IKrbUNl220El4Va_4Mqw-BgdfDY29J_IHj9l-CA4PIhBTctT5wegudHUMeQUsRejdEOJRzFqFryVr-i_pN3Uby8u9y0H9D85u_DLsC7IzAHV14-XbtpxqgKe-3D_D9fxZqaqftvwn8C4PzD3w</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Disu, E</creator><creator>Kehinde, O</creator><creator>Anga, A</creator><creator>Ubuane, P</creator><creator>Itiola, A</creator><creator>Akinola, I</creator><creator>Falase, B</creator><general>Wolters Kluwer India Pvt. Ltd</general><general>Medknow Publications and Media Pvt. Ltd</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>20191101</creationdate><title>Congenital pulmonary airway malformation: A case report of a rare cause of neonatal respiratory distress and review of the literature</title><author>Disu, E ; Kehinde, O ; Anga, A ; Ubuane, P ; Itiola, A ; Akinola, I ; Falase, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-ad7c60c2d5d85351443aa035d45cabb4ddec6dc15bca5ee69c6e6f8e75ea04a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Chest x-rays</topic><topic>Cystic Adenomatoid Malformation of Lung, Congenital - diagnosis</topic><topic>Cystic Adenomatoid Malformation of Lung, Congenital - diagnostic imaging</topic><topic>Cystic Adenomatoid Malformation of Lung, Congenital - surgery</topic><topic>Female</topic><topic>Genetic disorders</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Infants</topic><topic>Lung - diagnostic imaging</topic><topic>Lung - pathology</topic><topic>Male</topic><topic>Newborn infants</topic><topic>Nigeria</topic><topic>Rare Diseases</topic><topic>Respiratory Distress Syndrome, Newborn - etiology</topic><topic>Respiratory Insufficiency</topic><topic>Tomography, X-Ray Computed - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Disu, E</creatorcontrib><creatorcontrib>Kehinde, O</creatorcontrib><creatorcontrib>Anga, A</creatorcontrib><creatorcontrib>Ubuane, P</creatorcontrib><creatorcontrib>Itiola, A</creatorcontrib><creatorcontrib>Akinola, I</creatorcontrib><creatorcontrib>Falase, B</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>Nigerian journal of clinical practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Disu, E</au><au>Kehinde, O</au><au>Anga, A</au><au>Ubuane, P</au><au>Itiola, A</au><au>Akinola, I</au><au>Falase, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Congenital pulmonary airway malformation: A case report of a rare cause of neonatal respiratory distress and review of the literature</atitle><jtitle>Nigerian journal of clinical practice</jtitle><addtitle>Niger J Clin Pract</addtitle><date>2019-11-01</date><risdate>2019</risdate><volume>22</volume><issue>11</issue><spage>1621</spage><epage>1625</epage><pages>1621-1625</pages><issn>1119-3077</issn><abstract>Congenital pulmonary airway malformation (CPAM), formerly known as congenital cystic adenomatoid malformation (CCAM), is a rare developmental dysplastic lesion of the fetal tracheobronchial tree. CPAM is a rare cause of neonatal respiratory distress; however, its presence may span fetal to adult period. In two previous case-reports from Nigeria, CPAM was present in post-neonatal infants. We report the case of a neonate, who presented with increasing respiratory distress and an abnormal chest radiograph, initially assumed as pneumonic changes. A revised diagnosis of CPAM was made after a chest computed tomography (CT) scan. The neonate subsequently had a successful excision of the affected lobe with remarkable clinical improvement. The case highlights the need to utilize superior imaging studies such as CT when plain radiographs are inconclusive.</abstract><cop>India</cop><pub>Wolters Kluwer India Pvt. Ltd</pub><pmid>31719287</pmid><doi>10.4103/njcp.njcp_20_19</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1119-3077 |
| ispartof | Nigerian journal of clinical practice, 2019-11, Vol.22 (11), p.1621-1625 |
| issn | 1119-3077 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_2314252960 |
| source | MEDLINE; African Journals Online (Open Access); EZB-FREE-00999 freely available EZB journals |
| subjects | Chest x-rays Cystic Adenomatoid Malformation of Lung, Congenital - diagnosis Cystic Adenomatoid Malformation of Lung, Congenital - diagnostic imaging Cystic Adenomatoid Malformation of Lung, Congenital - surgery Female Genetic disorders Humans Infant, Newborn Infants Lung - diagnostic imaging Lung - pathology Male Newborn infants Nigeria Rare Diseases Respiratory Distress Syndrome, Newborn - etiology Respiratory Insufficiency Tomography, X-Ray Computed - methods |
| title | Congenital pulmonary airway malformation: A case report of a rare cause of neonatal respiratory distress and review of the literature |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-03T02%3A07%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Congenital%20pulmonary%20airway%20malformation:%20A%20case%20report%20of%20a%20rare%20cause%20of%20neonatal%20respiratory%20distress%20and%20review%20of%20the%20literature&rft.jtitle=Nigerian%20journal%20of%20clinical%20practice&rft.au=Disu,%20E&rft.date=2019-11-01&rft.volume=22&rft.issue=11&rft.spage=1621&rft.epage=1625&rft.pages=1621-1625&rft.issn=1119-3077&rft_id=info:doi/10.4103/njcp.njcp_20_19&rft_dat=%3Cgale_proqu%3EA605798435%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2314252960&rft_id=info:pmid/31719287&rft_galeid=A605798435&rfr_iscdi=true |