Rodgers B M, Harman P K, Johnson A M
Ann Surg. 1986 May;203(5):517-24. doi: 10.1097/00000658-198605000-00011.
Ventral anomalies of accessory pulmonary tissue have been classified as "bronchopulmonary foregut malformations." Between July 1, 1981, and May 31, 1985, 10 children with bronchopulmonary malformations have been cared for on the Pediatric Surgical Service at the University of Virginia. Six patients had bronchogenic cysts, one in an extrathoracic location and one associated with a pulmonary sequestration. Diagnosis was suspected in each case by plain chest radiographs and confirmed by computed tomography scans and ultrasound. Four patients had pulmonary sequestrations, two in association with diaphragmatic hernias. One patient had accessory pulmonary tissue, best classified as a tracheal lobe. Diagnosis in this patient was confirmed by bronchography. Nine patients underwent excision of the malformation without event. In one patient, a bronchogenic cyst was treated successfully by thoracoscopy. Review of the anatomy of these malformations leads to the conclusion that three embryologic events are cardinal in determining their ultimate form: (1) investment of the anomalous pulmonary tissue by the pulmonary artery; (2) the degree of involution of the original foregut communication; and (3) the stage of development leading to pleural investment.
副肺组织的腹侧异常已被归类为“支气管肺前肠畸形”。1981年7月1日至1985年5月31日期间,弗吉尼亚大学儿科外科收治了10例支气管肺畸形患儿。6例为支气管囊肿,1例位于胸外,1例合并肺隔离症。每例均通过胸部X线平片怀疑诊断,并经计算机断层扫描和超声证实。4例为肺隔离症,2例合并膈疝。1例有副肺组织,最适合归类为气管叶。该患者经支气管造影确诊。9例患者顺利接受了畸形切除术。1例支气管囊肿患者通过胸腔镜成功治疗。对这些畸形的解剖结构进行回顾后得出结论,有三个胚胎学事件在决定其最终形态方面至关重要:(1) 异常肺组织被肺动脉包绕;(2) 原始前肠通道的退化程度;(3) 导致胸膜包绕的发育阶段。