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It is not pneumothorax: Multicystic lung lesion in a six-year-old child
Author(s) -
Eman Sobh,
Amira Bahour,
Shady E. Anis
Publication year - 2016
Publication title -
proceedings of singapore healthcare
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
eISSN - 2059-2329
pISSN - 2010-1058
DOI - 10.1177/2010105816664357
Subject(s) - medicine , congenital cystic adenomatoid malformation , lung , pneumothorax , lesion , abnormality , airway , resection , cystic fibrosis , radiology , pathology , surgery , fetus , pregnancy , genetics , psychiatry , biology
Congenital cystic adenomatoid malformation (CCAM) – recently reported as congenital pulmonary airway malformation – is a rare abnormality of lung development. We present a case of a six-year-old child having a cystic lung lesion that proved to be CCAM after surgical resection. The child is performing well on follow-up.

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