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Currarinot triade

机译:Currarinot三合会

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摘要

A 14-year-old girl presented with severe abdominal pain and bilious vomiting at our institute. Her symptoms first started 48 h after eating lunch. She had runny bowel movements twice daily; her bowel habits appeared normal to her and her family. Her past medical history included a low imperforate anus and spina bifida with a neurogenic bladder. At a different hospital, she was given oral antibiotics for a suspected urinary tract infection; at no time did she complain of dysuria.On arrival, she complained about worsened abdominal pain. She had mild lower-abdominal tenderness to palpation and rectal examination revealed a stenosed anus. Her vital signs were stable and she was afebrile. Urine analysis and laboratory studies were unremarkable. An abdominal X-ray (Fig. 1) showed massive dilatation of the colorectum and a partial asymmetric deformity of the sacrum. Magnetic resonance imaging (MRI) studies confirmed these findings and revealed a tethered cord.
机译:我们研究所的一名14岁女孩表现出严重的腹痛和胆汁性呕吐。她的症状首先在午餐后48小时开始。她每天两次排便。她的排便习惯对她和她的家人来说是正常的。她过去的病史包括低位无孔肛门和具有神经源性膀胱的脊柱裂。在另一家医院,她因怀疑尿路感染而接受了口服抗生素治疗。她从来没有抱怨排尿困难,到达后就抱怨腹部疼痛加重。她有轻度的下腹部触诊压痛,直肠检查显示肛门狭窄。她的生命体征稳定并且发热。尿液分析和实验室研究无异常。腹部X线片(图1)显示了结直肠的大量扩张和ac骨的部分不对称畸形。磁共振成像(MRI)研究证实了这些发现,并揭示了系绳。

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