High anorectal malformation in a five-month-old boy: a case report
نویسندگان
چکیده
INTRODUCTION Anorectal malformation, one of the most common congenital defects, may present with a wide spectrum of defects. Almost all male patients present within first few days of life. CASE PRESENTATION A five-month-old baby boy of Indian origin and nationality presented with anal atresia and associated rectourethral prostatic fistula. The anatomy of the malformation and our patient's good condition permitted a primary definitive repair of the anomaly. A brief review of the relevant literature is included. CONCLUSION Delayed presentation of a patient with high anorectal malformation is rare. The appropriate treatment can be rewarding.
منابع مشابه
Scrotal pearl is not always a sign of anorectal malformation: median raphe cyst.
Pearls of meconium can be seen on the raphe of the scrotum and are considered as a sign of anorectal malformation (ARM). Scrotal pearls without ARM are rare in children and designated as median raphe cyst of the scrotum (MRC). A six-month-old boy with scrotal pearls without ARM is presented to discuss the clinical features and treatment modalities of MRC in infants.
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