| Congenital cystic adenomatoid malformation. Report of two cases and review of the literature. | |
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MedLine Citation:
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PMID: 9677737 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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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. |
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Authors:
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B Kiliçarslan; M Yaz; N Paksoy |
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Publication Detail:
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Type: Case Reports; Journal Article; Review |
Journal Detail:
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Title: The Turkish journal of pediatrics Volume: 40 ISSN: 0041-4301 ISO Abbreviation: Turk. J. Pediatr. Publication Date: 1998 Apr-Jun |
Date Detail:
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Created Date: 1998-08-20 Completed Date: 1998-08-20 Revised Date: 2005-11-16 |
Medline Journal Info:
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Nlm Unique ID: 0417505 Medline TA: Turk J Pediatr Country: TURKEY |
Other Details:
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Languages: eng Pagination: 289-94 Citation Subset: IM |
Affiliation:
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Department of Patholoogy, Akdeniz University Faculty of Medicine, Antalya, Turkey. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Cyanosis
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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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