Document Detail


Congenital cystic adenomatoid malformation. Report of two cases and review of the literature.
MedLine Citation:
PMID:  9677737     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Congenital cystic adenomatoid malformation (CCAM) of the lung is a rare pulmonary lesion, characterized by an excessive overgrowth of the terminal respiratory bronchioles. The lesion is almost always unilateral and may occur in any lobe. We present two children with CCAM. The first case was a one-day-old female infant admitted with respiratory distress and cyanosis. The second case was a 19-month-old girl with a nine-month history of recurrent respiratory infections. Preoperative diagnosis of both cases was intrapulmonary mass. The histopathological examinations revealed CCAM.
Authors:
B Kiliçarslan; M Yaz; N Paksoy
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Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  The Turkish journal of pediatrics     Volume:  40     ISSN:  0041-4301     ISO Abbreviation:  Turk. J. Pediatr.     Publication Date:    1998 Apr-Jun
Date Detail:
Created Date:  1998-08-20     Completed Date:  1998-08-20     Revised Date:  2005-11-16    
Medline Journal Info:
Nlm Unique ID:  0417505     Medline TA:  Turk J Pediatr     Country:  TURKEY    
Other Details:
Languages:  eng     Pagination:  289-94     Citation Subset:  IM    
Affiliation:
Department of Patholoogy, Akdeniz University Faculty of Medicine, Antalya, Turkey.
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MeSH Terms
Descriptor/Qualifier:
Cyanosis / etiology
Cystic Adenomatoid Malformation of Lung, Congenital / classification,  complications,  diagnosis*,  embryology,  surgery
Female
Humans
Infant, Newborn
Recurrence
Respiratory Insufficiency / etiology
Respiratory Tract Infections / etiology

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