Document Detail


Unilateral pulmonary artery agenesis with presentation of hemoptysis: a case report.
MedLine Citation:
PMID:  10502857     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Unilateral pulmonary artery agenesis (UPAA), a rare congenital anomaly frequently associated with other cardiovascular abnormalities, is usually diagnosed and surgically treated in childhood. Those who do not suffer other cardiac anomalies (isolated UPAA) have only minor or no symptoms and survive into adulthood. Isolated UPAA in adult patients may present as recurrent respiratory tract infection, dyspnea on exertion, hemoptysis or an incidental finding of an abnormal chest radiograph. We present the case of a 38-year-old man with a congenital absence of the right pulmonary artery (PA) and recurrent hemoptysis. The diagnosis was confirmed by cardiac catheterization, which disclosed an absence of the right PA and systemic collaterals to the right lung from the right internal thoracic artery and posterior intercostal arteries.
Authors:
Y M Lin; K W Liang; C T Ting
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Zhonghua yi xue za zhi = Chinese medical journal; Free China ed     Volume:  62     ISSN:  0578-1337     ISO Abbreviation:  Zhonghua Yi Xue Za Zhi (Taipei)     Publication Date:  1999 Sep 
Date Detail:
Created Date:  1999-10-13     Completed Date:  1999-10-13     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0005327     Medline TA:  Zhonghua Yi Xue Za Zhi (Taipei)     Country:  CHINA    
Other Details:
Languages:  eng     Pagination:  644-7     Citation Subset:  IM    
Affiliation:
Department of Medicine, Hsing Feng Hospital, Feng Yuan, Taichung, Taiwan, ROC.
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MeSH Terms
Descriptor/Qualifier:
Adult
Heart Catheterization
Hemoptysis / etiology*
Humans
Male
Pulmonary Artery / abnormalities*

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