A Communicating Bronchopulmonary Foregut Malformation Associated with Absence of the Left Pericardium: A case report / 대한흉부외과학회지
Dong-Gon YOO; Chong-Wook KIM; Chong-Bin PARK; Pil-Je KANG; Jong-Hyeog LEE.
The Korean Journal of Thoracic and Cardiovascular Surgery
; : 793-797, 2007.
Artículo
en Ko
| WPRIM | ID: wpr-133375
A communicating bronchopulmonary foregut malformation (CBPFM) is a rare congenital anomaly that is characterized by a fistula between isolated respiratory tissue and the esophagus or stomach. The presence of accessory lung tissue arising from the primitive gastrointestinal tube is a common factor in the development of all forms of bronchopulmonary foregut malformations. Recurrent pneumonia associated with cystic radiographic structures is a characteristic of the condition. Further imaging studies using esophagogram, bronchography, computerized tomography, MRI, and arteriography can help in making a diagnostic evaluation. The treatment is a surgical resection of the involved lung tissue, and fistula closure with a good prognosis. We encountered a case of CBPFM, who presented with an extralobar pulmonary sequestration and bronchogenic cyst communicating with a tubular esophageal duplication that was associated with a complete left pericardial defect.
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