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نوع الدراسة
النطاق السنوي
3.
مقالة ي الانجليزية | IMSEAR | ID: sea-138670

الملخص

Congenital cystic adenomatoid malformation (CCAM) encompasses a continuum of hamartomatous cystic lung lesions characterised by the presence of abnormal bronchiolar structures of varying sizes or distribution. The CCAM is a disorder of infancy with majority of the cases being diagnosed within the first two years of life. We describe CCAM in a 13-yearold girl complaining of recurrent lower respiratory tract infections since infancy who presented with post-infectious pneumatocele with loculated pleural effusion, and suspected abscess formation and had undergone resection.


الموضوعات
Adolescent , Cystic Adenomatoid Malformation of Lung, Congenital/complications , Cystic Adenomatoid Malformation of Lung, Congenital/diagnosis , Cystic Adenomatoid Malformation of Lung, Congenital/surgery , Diagnosis, Differential , Female , Humans , Lung Abscess/diagnosis , Lung Abscess/etiology , Lung Abscess/surgery , Photomicrography , Pleural Effusion/diagnosis , Pleural Effusion/etiology , Pleural Effusion/surgery , Radiography, Thoracic , Thoracotomy/methods , Tomography, X-Ray Computed
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