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Unusual presentation of more common disease/injury: A newer variant of congenital pouch colon with rectal agenesis: management strategy and review of the literature

机译:不同寻常的疾病/损伤的异常表现:先天性小肠结肠变种伴直肠发育不全的新变体:治疗策略和文献复习

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摘要

A 3-day-old male baby presented with clinico-radiological features of rectal atresia with colo-urinary fistula. There was no radiological evidence of congenital pouch colon (CPC), but per-operatively CPC of unusual anatomy was found. The CPC was intermediate between type I and type II of Narsimha’s classification. The pouch had rudimentary appendix and proximal colovesical fistula. The distal end of CPC was free. In the first stage, diverting ileostomy was done. In follow-up, after 1 month because of rectourinary fistula baby developed hyperchloremic metabolic acidosis and uremic sepsis. First metabolic correction and control of sepsis were done. Thereafter, abdomino-posterior saggital approach was used for excision of colovesical fistula, appendectomy, coloplasty and colorectal anastmosis. The ileostomy was left undisturbed. The infant at present is waiting for the third stage ileostomy closure.
机译:一名3天大的男婴表现出直肠闭锁伴结肠泌尿瘘的临床放射学特征。没有放射学证据显示先天性袋结肠(CPC),但在手术中发现了异常解剖的CPC。 CPC介于Narsimha的I类和II类之间。该小袋具有基本的阑尾和近侧的loveslove瘘。 CPC的远端是自由的。在第一阶段,进行了转向回肠造口术。在随访中,由于直肠瘘1个月后,婴儿出现了高氯代谢性酸中毒和尿毒症败血症。首先进行了代谢纠正和败血症控制。此后,采用腹-后矢状入路切除肠膜瘘,阑尾切除术,结肠成形术和结直肠吻合术。回肠造口术不受干扰。目前该婴儿正在等待第三阶段回肠造口术关闭。

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