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Malformation anorectale avec fistule recto-uretro-bulbaire prise en charge tardivement: à propos dun cas

机译:输尿管直肠瘘肛肠畸形晚期治疗一例

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摘要

Ano-rectale malformations (ARM) are a spectrum of heterogeneous abnormalities in the development of the rectal canal. Its incidence is usually low and it is a little higher in some developing countries. Boys are more affected than girls and rectobulbar fistula associated with atresia of the anal canal is the most frequent disorder among them. We report the case of a 10-months old infant of male sex, whose mother lived in a mining area and had been complaining of fecaluria since the birth of her child. Physical examination showed fingerprint 1 cm below the intersection of the median raphe and the bi-ischiatic line. Paraclinical examinations showed no other associated malformation. Patient's management was based on anorectoplasty through abdominal and perineal approach with lower abdominoperineal reconstruction. In the post-operative period, the patient received antibiotic treatment and intravenous analgesia as well as dilations, which continued after discharge 2 weeks after surgery. No complications were observed and outcome was favorable.
机译:直肠直肠畸形(ARM)是直肠管发育过程中的一系列异质异常。它的发病率通常较低,在某些发展中国家则较高。男孩比女孩受到的影响更大,与肛管闭锁相关的直肠瘘是其中最常见的疾病。我们报告了一例10个月大的男婴,其母亲住在矿区,自从她的孩子出生以来就一直抱怨粪便。体格检查显示指纹在中线和双坐骨线的交点下方1厘米处。旁临床检查未发现其他相关的畸形。患者的治疗基于通过腹部和会阴入路的肛门直肠成形术,并进行下腹部手术重建。术后,患者接受了抗生素治疗,静脉镇痛以及扩张,术后2周出院后继续进行。未观察到并发症,预后良好。

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