Congenital bilio-bronchial fistula in an adult: a review of literature and video demonstration of laparoscopic fistula tract excision.

Chandrasekar Murugesan, Muniza Bai, Biju Pottakkat, Dharm Prakash Dwivedi, Hemachandren Munuswamy, Pazhanivel Mohan
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Abstract

This article presents a review of the literature on congenital bilio-bronchial fistula (BBF), a rare anomaly characterized by abnormal communication between the bile duct and respiratory tract. Congenital BBF often presents with bilioptysis in early neonates and infants; however, patients with no overt symptoms may occasionally present in adulthood. Our literature search in Medline from 1850 to 2023 revealed 42 reported cases of congenital BBF, primarily managed with thoracotomy and excision of the fistula tract. About one-third of these cases required multiple surgeries due to associated biliary anomalies. The review underscores the importance of diagnostic imaging, including bronchoscopy, in identifying and delineating the extent of the fistula. It also highlights the evolving surgical management, with recent cases showing the efficacy of minimally invasive approaches such as laparoscopy and thoracoscopy. In addition to the literature review, we report a young female patient with a history of recurrent respiratory infections presenting with bilioptysis and extensive left lung damage. Initial management included bronchoscopy-guided glue instillation, left thoracotomy, and pneumonectomy. Following the recurrence of symptoms, the patient was successfully treated with laparoscopic excision of the fistula tract. In recent times, minimally invasive approaches such as laparoscopy and thoracoscopy, with excision of the fistula tract are gaining popularity and have shown good results. We suggest biliary communication being the high-pressure end, tackling it transabdominal may prevent recurrent problems.

成人先天性双侧支气管瘘:文献综述和腹腔镜瘘道切除术视频演示。
本文综述了有关先天性胆-支气管瘘(BBF)的文献,BBF 是一种罕见的畸形,其特点是胆管和呼吸道之间的沟通异常。先天性胆-支气管瘘通常在新生儿早期和婴儿期表现为胆汁性咯血;但也有患者在成年后偶尔会出现无明显症状的情况。我们在 Medline 上搜索了 1850 年至 2023 年的文献,发现有 42 例先天性 BBF 的报道,主要是通过开胸手术和切除瘘管道进行治疗。其中约三分之一的病例因伴有胆道异常而需要多次手术。综述强调了诊断成像(包括支气管镜)在识别和划定瘘管范围方面的重要性。它还强调了不断发展的手术治疗方法,最近的病例显示了腹腔镜和胸腔镜等微创方法的疗效。除了文献综述外,我们还报告了一名年轻女性患者,她有反复呼吸道感染病史,并伴有胆汁淤积和广泛的左肺损伤。最初的治疗包括支气管镜引导下的胶水灌注、左胸切开术和肺切除术。症状复发后,患者成功接受了腹腔镜下瘘道切除术。近来,腹腔镜和胸腔镜等微创方法在切除瘘管道方面越来越受欢迎,并取得了良好的效果。我们认为,胆道沟通是高压端,经腹处理可防止问题复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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