Anorectal Malformation: Paediatric Problem Presenting in Adult

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Anorectal Malformation: Paediatric Problem Presenting in Adult

This is a case report of 22-year-old girl admitted with abdominal distension, vomiting, and chronic constipation since birth. Abdomen was distended, and perineal examination revealed imperforate anus with vestibular fistula (ARM). So far worldwide very few cases have been reported about anorectal malformation presenting in adulthood, and thus extremely little data is available in the literature...

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Delayed diagnosis of anorectal malformation--a persistent problem.

Delayed diagnosis of anorectal malformation (ARM) is an avoidable event associated with significant complications and morbidity. Previous studies have suggested higher than expected rates of delayed diagnosis, especially when a threshold of 24 hours of life is used to define delayed diagnosis. The aim of this study is to highlight the prevalence of delayed diagnosis of ARM in Ireland and to det...

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Polypoid Arteriovenous Malformation Presenting with Jejunojejunal Intussusceptions in an Adult

Jejunal polypoid arteriovenous malformations (AVMs) and jejunojejunal intussusceptions are both rare. Here, we present the case of a 61-year-old woman who suffered intermittent episodes of abdominal pain over the course of 13 years. A computed tomography scan of her abdomen and pelvis revealed a distal jejunojejunal intussusception. A suspected low density mass was observed at the tip of the in...

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Rectal Stenosis: A Rare Anorectal Malformation

A 2-day-old male baby presented with abdominal distension and failure to pass meconium. The perineal examination revealed normally placed patent anus. A rectal examination with thermometer revealed a resistance at 2-3cm from the anal verge. A contrast enema was given to document the suspicion of rectal atresia. The contrast enema revealed a 2cm long stenosis of the rectum opening abruptly into ...

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Malformation anorectale et complexe sphinctérien anorectal

We report the case of a patient referred to our prenatal diagnostic unit due to the suspicion of spina bifida at 24 weeks gestation. Morphological assessment revealed rachischisis associated with Chiari type II, single kidney and anorectal malformation. The nonvisualization of the anal sphincter complex (ASC) on ultrasound led to the diagnosis of suspected high-type anorectal malformation (A,B ...

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ژورنال

عنوان ژورنال: Case Reports in Surgery

سال: 2015

ISSN: 2090-6900,2090-6919

DOI: 10.1155/2015/625474