Rideout D T, Hayashi A H, Gillis D A, Giacomantonio J M, Lau H Y
Department of Surgery, IWK Children's Hospital, Halifax, Nova Scotia, Canada.
J Pediatr Surg. 1991 Nov;26(11):1303-5. doi: 10.1016/0022-3468(91)90605-s.
The association of tracheomalacia (TM) with esophageal atresia (EA) has been well described. This study attempted to find a correlation between the severity of TM and the presence or absence of an associated tracheoesophageal fistula (TEF) in patients with EA. A review of all patients presenting at this institution with EA through the years 1970 to 1990 was carried out. Six patients with EA without fistula (type A) and 61 patients having EA with fistula (types B, C, D, and E) were analyzed. Five of the six type A patients required esophageal dilatations and antireflux procedures; none had clinically significant TM. Thirty-five of the 61 patients with fistula required esophageal dilatation, and 8 had an antireflux procedure; 11 (18%) required either long-tube tracheostomy or aortopexy for TM. This small study supports a recent hypothesis of different embryological events resulting in different types of esophageal and tracheal anomalies. When EA occurs without fistula, it appears that no significant alteration in tracheal development occurs.
气管软化(TM)与食管闭锁(EA)之间的关联已得到充分描述。本研究试图在EA患者中寻找TM严重程度与是否存在相关气管食管瘘(TEF)之间的相关性。对1970年至1990年期间在本机构就诊的所有EA患者进行了回顾。分析了6例无瘘的EA患者(A型)和61例有瘘的EA患者(B型、C型、D型和E型)。6例A型患者中有5例需要进行食管扩张和抗反流手术;均无临床显著的TM。61例有瘘患者中有35例需要进行食管扩张,8例进行了抗反流手术;11例(18%)因TM需要进行长管气管切开术或主动脉固定术。这项小型研究支持了最近的一种假说,即不同的胚胎学事件导致了不同类型的食管和气管异常。当EA无瘘发生时,气管发育似乎没有明显改变。