OC157: Bronchopulmonary sequestration and congenital cystic adenomatoid malformation: Natural History

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Aberrant cell adhesion molecule expression in human bronchopulmonary sequestration and congenital cystic adenomatoid malformation.

In many organs, integrins and cadherins are partly regulated by Hox genes, but their interactions in airway morphogenesis and congenital lung diseases are unknown. We previously showed that the Hox protein HoxB5 is abnormally increased in bronchopulmonary sequestration (BPS) and congenital cystic adenomatoid malformation (CCAM), congenital lung lesions with abnormal airway branching. We now rep...

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Congenital cystic adenomatoid malformation

Australasian Journal of Ultrasound in Medicine August 2009; 12 (3) Introduction Congenital cystic adenomatoid malformation (CCAM) is an uncommon fetal lung anomaly involving cystic changes to the terminal bronchioles. The condition requires close monitoring during the antenatal period with ultrasound in addition to input from the neonatal and paediatric surgical teams. This case study involves ...

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Adult-Onset Congenital Cystic Adenomatoid Malformation in Combination with Intralobar Bronchopulmonary Sequestration: a case report

Congenital cystic adenomatoid malformation (CCAM) and bronchopulmonary sequestration are congenital lung lesions. They are classified as separate entities. Each of them has distinct embryology, pathology, and natural history. However there are some commonalities between them. CCAM may have a pulmonary artery supply, or be supplied like a sequestration from the aorta, and histological features o...

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Congenital Cystic Adenomatoid Malformation (CCAM) with Two Cases Introduction

CCAM is a rare conolition in the neonatal Period. Two babies were admitted to Mofid hospital with cyanosis and respiratory distress. Pneumectomy was done for both of them for space occupaying lesion. Pathology examination of first case showed area of cuboidal epithelium lined tubes and spaces resembling fetal bronchioles, which are torn in folds. In second case, pathologic examination revealed...

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[Congenital cystic adenomatoid malformation: a case report].

Cystic adenomatoid malformation is a rare pulmonary hamartomatous lesion, of an unknown etiology. Report a singular case of CAM of one newborn, with marked respiratory distress. Using different method (chest X-ray, Multidetector row CT associated at multiplanar and three-dimensional reconstructions), we obtained an accurate diagnosis of site and nature, critical for a correct therapeutic approach.

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ژورنال

عنوان ژورنال: Ultrasound in Obstetrics and Gynecology

سال: 2008

ISSN: 0960-7692,1469-0705

DOI: 10.1002/uog.5565