Cossentino M J, Ormseth E J, Tavaf-Motamen H, Cheney C P
Department of Medicine, Walter Reed Army Medical Center, Washington, DC 20307, USA.
Am J Gastroenterol. 2000 Aug;95(8):2116-8. doi: 10.1111/j.1572-0241.2000.02022.x.
Congenital bronchoesophageal fistula is a rare anomaly that may go undiagnosed for many years. There are <200 reported cases in the literature. Patients usually present with chronic cough, a history of multiple pneumonias, and, less often, hemoptysis. The most sensitive test to diagnose a bronchoesophageal fistula is barium esophagogram. Surgical resection is the treatment of choice and is definitive in almost all cases. We present the case of a 52-yr-old woman with a history of cough and multiple pneumonias who sought medical treatment for abdominal pain. We discuss the presentation and the radiographic, endoscopic, and surgical findings, along with a review of the literature.
先天性支气管食管瘘是一种罕见的畸形,可能多年未被诊断。文献报道的病例<200例。患者通常表现为慢性咳嗽、多次肺炎病史,咯血则较少见。诊断支气管食管瘘最敏感的检查是钡剂食管造影。手术切除是首选治疗方法,几乎在所有病例中都是决定性的。我们报告了一例52岁女性患者,有咳嗽和多次肺炎病史,因腹痛寻求治疗。我们讨论了其临床表现、影像学、内镜及手术检查结果,并对文献进行了综述。