Neonatal spontaneous biliary perforation: Case report

F. Reyna-Sepúlveda, A. Esparza-González, V. Govea-Ortiz, G. Martínez-Flores, F. Montes-Tapia, U. Garza-Luna, G. Muñoz-Maldonado
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引用次数: 2

Abstract

Objective

Spontaneous biliary perforation in neonates is rare. The etiology of this pathology is idiopathic and various management strategies ranging from non-operative treatment to complex operations, such as biliary-enteric reconstruction, are performed, with few reported outcomes.

Case report

A 3-week-old female, born at term, presented fever, abdominal distension, and acholic stool. An ultrasound was performed, which revealed generalized ascites and a poorly-defined collection. An emergency laparotomy confirmed perforation in the distal common bile duct and a biliary-enteric-anastomosis was performed.

Discussion

Wide drainage has been reported as the best initial management strategy for spontaneous biliary perforation, although it depends on the patient's clinical status and intraoperative findings.

Conclusions

Spontaneous infantile biliary perforation is rare. Main management is wide drainage with, most perforations being resolved in 2 weeks.

新生儿自发性胆道穿孔1例
目的新生儿自发性胆道穿孔较为少见。这种病理的病因是特发性的,各种各样的治疗策略,从非手术治疗到复杂的手术,如胆道-肠重建,被执行,很少报道的结果。病例报告:一名足月出生的3周大女婴,出现发烧、腹胀和胆汁性大便。行超声检查,发现广泛性腹水和不明确的集合。急诊开腹确认胆总管远端穿孔,并行胆肠吻合术。广泛引流已被报道为自发性胆道穿孔的最佳初始治疗策略,尽管这取决于患者的临床状况和术中发现。结论小儿自发性胆道穿孔少见。主要处理方法是广泛引流,大多数穿孔在2周内解决。
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