Pulmonary vascular disorders masquerading as interstitial lung disease
During the acquisition of a series of 92 children with interstitial lung disease (ILD) over a 14 year period, a significant minority (8/92 or 9%) were initially diagnosed as having ILD, but were subsequently found to have a variety of arterial, venous, and/or capillary disorders that explained their...
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| Veröffentlicht in: | Pediatric pulmonology 1995-11, Vol.20 (5), p.284-288 |
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| container_title | Pediatric pulmonology |
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| creator | Sondheimer, Henry M. Lung, M. Colleen Lum Brugman, Susan M. Iklé, David N. Fan, Leland L. White, Carl W. |
| description | During the acquisition of a series of 92 children with interstitial lung disease (ILD) over a 14 year period, a significant minority (8/92 or 9%) were initially diagnosed as having ILD, but were subsequently found to have a variety of arterial, venous, and/or capillary disorders that explained their initial pulmonary findings. This subgroup of patients has had a very high morbidity and mortality, with only three of eight patients currently surviving. The presentation, evaluation, and natural history of these eight children were reviewed. We developed a strategy of cardiac and pulmonary evaluation for children presenting with clinical and radiographic features of ILD that helped us to identify rapidly those with pulmonary vascular disorders. Pediatr Pulmonol. 1995; 20:284–288. © 1995 Wiley‐Liss, Inc. |
| doi_str_mv | 10.1002/ppul.1950200505 |
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Colleen Lum ; Brugman, Susan M. ; Iklé, David N. ; Fan, Leland L. ; White, Carl W.</creator><creatorcontrib>Sondheimer, Henry M. ; Lung, M. Colleen Lum ; Brugman, Susan M. ; Iklé, David N. ; Fan, Leland L. ; White, Carl W.</creatorcontrib><description>During the acquisition of a series of 92 children with interstitial lung disease (ILD) over a 14 year period, a significant minority (8/92 or 9%) were initially diagnosed as having ILD, but were subsequently found to have a variety of arterial, venous, and/or capillary disorders that explained their initial pulmonary findings. This subgroup of patients has had a very high morbidity and mortality, with only three of eight patients currently surviving. The presentation, evaluation, and natural history of these eight children were reviewed. We developed a strategy of cardiac and pulmonary evaluation for children presenting with clinical and radiographic features of ILD that helped us to identify rapidly those with pulmonary vascular disorders. 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Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases ; pulmonary veno-occlusive disease ; Pulmonary Veno-Occlusive Disease - diagnosis ; Pulmonary Veno-Occlusive Disease - physiopathology ; Retrospective Studies ; Risk Factors ; Survival Rate ; Telangiectasia, Hereditary Hemorrhagic - diagnosis ; Telangiectasia, Hereditary Hemorrhagic - physiopathology</subject><ispartof>Pediatric pulmonology, 1995-11, Vol.20 (5), p.284-288</ispartof><rights>Copyright © 1995 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4115-56e24d6fd1315d5dbb1a3ad54d458bce86e0394da8516d383750a7131bdc00d53</citedby><cites>FETCH-LOGICAL-c4115-56e24d6fd1315d5dbb1a3ad54d458bce86e0394da8516d383750a7131bdc00d53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fppul.1950200505$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fppul.1950200505$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>309,310,314,780,784,789,790,1417,23930,23931,25140,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3030780$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8903899$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sondheimer, Henry M.</creatorcontrib><creatorcontrib>Lung, M. Colleen Lum</creatorcontrib><creatorcontrib>Brugman, Susan M.</creatorcontrib><creatorcontrib>Iklé, David N.</creatorcontrib><creatorcontrib>Fan, Leland L.</creatorcontrib><creatorcontrib>White, Carl W.</creatorcontrib><title>Pulmonary vascular disorders masquerading as interstitial lung disease</title><title>Pediatric pulmonology</title><addtitle>Pediatr. Pulmonol</addtitle><description>During the acquisition of a series of 92 children with interstitial lung disease (ILD) over a 14 year period, a significant minority (8/92 or 9%) were initially diagnosed as having ILD, but were subsequently found to have a variety of arterial, venous, and/or capillary disorders that explained their initial pulmonary findings. This subgroup of patients has had a very high morbidity and mortality, with only three of eight patients currently surviving. The presentation, evaluation, and natural history of these eight children were reviewed. We developed a strategy of cardiac and pulmonary evaluation for children presenting with clinical and radiographic features of ILD that helped us to identify rapidly those with pulmonary vascular disorders. Pediatr Pulmonol. 1995; 20:284–288. © 1995 Wiley‐Liss, Inc.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular Diseases - diagnosis</subject><subject>Cardiovascular Diseases - physiopathology</subject><subject>Child</subject><subject>Chronic Disease</subject><subject>Diagnosis, Differential</subject><subject>Echocardiography</subject><subject>Electrocardiography</subject><subject>Hereditary hemorrhagic telangiectasia</subject><subject>Humans</subject><subject>Hypertension, Pulmonary - diagnosis</subject><subject>Hypertension, Pulmonary - physiopathology</subject><subject>Incidence</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Logistic Models</subject><subject>Lung Diseases, Interstitial - diagnosis</subject><subject>Lung Diseases, Interstitial - physiopathology</subject><subject>Medical sciences</subject><subject>Pneumology</subject><subject>pulmonary hemangiomatosis</subject><subject>pulmonary hypertension</subject><subject>Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases</subject><subject>pulmonary veno-occlusive disease</subject><subject>Pulmonary Veno-Occlusive Disease - diagnosis</subject><subject>Pulmonary Veno-Occlusive Disease - physiopathology</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Survival Rate</subject><subject>Telangiectasia, Hereditary Hemorrhagic - diagnosis</subject><subject>Telangiectasia, Hereditary Hemorrhagic - physiopathology</subject><issn>8755-6863</issn><issn>1099-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PGzEQhq0KlIaPc09Ie0C9LRnHa6-tnqqIAFIEqQriaM2uHeTWu5vau4X8e4wSBXHiZGnmecczDyHfKFxQgOlkvR78BVUcpgAc-BcypqBUDoUSB2QsS85zIQX7So5i_AOQeoqOyEgqYFKpMZkvB990LYZN9h9jPXgMmXGxC8aGmDUY_w02oHHtU4Yxc22fyr3rHfrMD6mYWIvRnpDDFfpoT3fvMXmYX97PrvPF3dXN7OcirwtKec6FnRZGrAxllBtuqooiQ8MLU3BZ1VYKC0wVBiWnwjDJSg5YJrgyNYDh7Jh8385dhy5tFnvduFhb77G13RB1KWgpVVEkcLIF69DFGOxKr4Nr0pmagn4zp9_M6XdzKXG2Gz1UjTV7fqcq9c93_eQJ_SpgW7u4xxgwKCUk7McWe3bebj77VS-XD4sPS-TbtIu9fdmnMfzVokw29OPtlV7Ar9-PM36vJXsFHBWYCQ</recordid><startdate>199511</startdate><enddate>199511</enddate><creator>Sondheimer, Henry M.</creator><creator>Lung, M. 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Colleen Lum ; Brugman, Susan M. ; Iklé, David N. ; Fan, Leland L. ; White, Carl W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4115-56e24d6fd1315d5dbb1a3ad54d458bce86e0394da8516d383750a7131bdc00d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Cardiovascular Diseases - diagnosis</topic><topic>Cardiovascular Diseases - physiopathology</topic><topic>Child</topic><topic>Chronic Disease</topic><topic>Diagnosis, Differential</topic><topic>Echocardiography</topic><topic>Electrocardiography</topic><topic>Hereditary hemorrhagic telangiectasia</topic><topic>Humans</topic><topic>Hypertension, Pulmonary - diagnosis</topic><topic>Hypertension, Pulmonary - physiopathology</topic><topic>Incidence</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Logistic Models</topic><topic>Lung Diseases, Interstitial - diagnosis</topic><topic>Lung Diseases, Interstitial - physiopathology</topic><topic>Medical sciences</topic><topic>Pneumology</topic><topic>pulmonary hemangiomatosis</topic><topic>pulmonary hypertension</topic><topic>Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases</topic><topic>pulmonary veno-occlusive disease</topic><topic>Pulmonary Veno-Occlusive Disease - diagnosis</topic><topic>Pulmonary Veno-Occlusive Disease - physiopathology</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Survival Rate</topic><topic>Telangiectasia, Hereditary Hemorrhagic - diagnosis</topic><topic>Telangiectasia, Hereditary Hemorrhagic - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sondheimer, Henry M.</creatorcontrib><creatorcontrib>Lung, M. 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Colleen Lum</au><au>Brugman, Susan M.</au><au>Iklé, David N.</au><au>Fan, Leland L.</au><au>White, Carl W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pulmonary vascular disorders masquerading as interstitial lung disease</atitle><jtitle>Pediatric pulmonology</jtitle><addtitle>Pediatr. Pulmonol</addtitle><date>1995-11</date><risdate>1995</risdate><volume>20</volume><issue>5</issue><spage>284</spage><epage>288</epage><pages>284-288</pages><issn>8755-6863</issn><eissn>1099-0496</eissn><coden>PEPUES</coden><abstract>During the acquisition of a series of 92 children with interstitial lung disease (ILD) over a 14 year period, a significant minority (8/92 or 9%) were initially diagnosed as having ILD, but were subsequently found to have a variety of arterial, venous, and/or capillary disorders that explained their initial pulmonary findings. This subgroup of patients has had a very high morbidity and mortality, with only three of eight patients currently surviving. The presentation, evaluation, and natural history of these eight children were reviewed. We developed a strategy of cardiac and pulmonary evaluation for children presenting with clinical and radiographic features of ILD that helped us to identify rapidly those with pulmonary vascular disorders. Pediatr Pulmonol. 1995; 20:284–288. © 1995 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>8903899</pmid><doi>10.1002/ppul.1950200505</doi><tpages>5</tpages></addata></record> |
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| subjects | Adolescent Biological and medical sciences Cardiovascular Diseases - diagnosis Cardiovascular Diseases - physiopathology Child Chronic Disease Diagnosis, Differential Echocardiography Electrocardiography Hereditary hemorrhagic telangiectasia Humans Hypertension, Pulmonary - diagnosis Hypertension, Pulmonary - physiopathology Incidence Infant Infant, Newborn Logistic Models Lung Diseases, Interstitial - diagnosis Lung Diseases, Interstitial - physiopathology Medical sciences Pneumology pulmonary hemangiomatosis pulmonary hypertension Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases pulmonary veno-occlusive disease Pulmonary Veno-Occlusive Disease - diagnosis Pulmonary Veno-Occlusive Disease - physiopathology Retrospective Studies Risk Factors Survival Rate Telangiectasia, Hereditary Hemorrhagic - diagnosis Telangiectasia, Hereditary Hemorrhagic - physiopathology |
| title | Pulmonary vascular disorders masquerading as interstitial lung disease |
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