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Updated: May 27, 2026

Development of Obliterative Bronchiolitis in a Murine Model of Orthotopic Lung Transplantation
Published on: July 10, 2012
Bronchopulmonary foregut malformation.
Yoshihiko Katayama1, Hitoshi Kusagawa, Takuya Komada
1Department of Thoracic Surgery, Matsusaka Chuo General Hospital, 102 Konozomu, Kawaimachi, Matsusaka, 515-0818, Japan. kataccho0209@yahoo.co.jp
Bronchopulmonary foregut malformation (BPFM) is a rare congenital anomaly. This case details an extralobar pulmonary sequestration (ELS) connected to the esophagus via a cyst, offering insights into its embryogenesis.
Area of Science:
- Medical Science
- Developmental Biology
- Thoracic Surgery
Background:
- Bronchopulmonary foregut malformation (BPFM) encompasses rare ventral anomalies of accessory pulmonary tissue, often originating from the esophagus or stomach.
- BPFM specifically describes sequestrations retaining gastrointestinal tract communication, typically via a muscular tube lined with squamous or columnar epithelium.
Observation:
- A rare case of extralobar pulmonary sequestration (ELS) in an adult is presented.
- The ELS was found to be connected to the esophagus through a cyst.
- This connecting cyst's inner wall featured both squamous and respiratory epithelium.
Findings:
- The study describes a unique BPFM case involving ELS connected to the esophagus by a foregut cyst.
- The cyst's dual epithelial lining (squamous and respiratory) suggests a specific embryogenic origin.
- This finding provides a detailed example of BPFM with a distinct anatomical connection.
Implications:
- Understanding the embryogenesis of BPFM is crucial for accurate diagnosis and surgical planning.
- This case highlights the importance of detailed histological examination of the connecting stalk in BPFM.
- Further research into these rare malformations can improve patient outcomes and diagnostic criteria.
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