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A Case of Cecal Volvulus Presenting with Chronic Constipation in Lissencephaly

机译:盲肠性慢性便秘的盲肠扭转一例

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摘要

Cecal volvulus is uncommon in pediatric patients and there are few reports of cecal volvulus with cerebral palsy. Here, we report the case of a 19-year-old male patient who presented with abdominal distension, a history of cerebral palsy, refractory epilepsy due to lissencephaly, and chronic constipation. An abdominal x-ray and computed tomography without contrast enhancement showed fixed dilated bowel intensity in the right lower abdomen. Despite decompression with gastric and rectal tube insertion, symptoms did not improve. The patient underwent an exploratory laparotomy that revealed cecal volvulus. Cecal volvulus usually occurs following intestinal malrotation or previous surgery. In this patient, however, intestinal distension accompanying mental disability and chronic constipation resulted in the development of cecal volvulus. We suggest that cecal and proximal large bowel volvulus should be considered in patients presenting with progressive abdominal distension combined with a history of neuro-developmental delay and constipation.
机译:盲肠肠扭转在小儿患者中并不常见,很少有盲肠肠扭转合并脑瘫的报道。在此,我们报道了一名19岁男性患者的病例,该患者出现腹胀,有脑瘫史,因小脑畸形导致的难治性癫痫病和慢性便秘。腹部X射线和计算机断层扫描未显示造影剂增强,显示右下腹部的固定肠扩张强度。尽管通过插入胃管和直肠管减压,但症状并未改善。患者进行了探查性盲肠肠探查术。盲肠扭转通常发生在肠旋转不良或先前的手术后。然而,在该患者中,伴随智力障碍和慢性便秘的肠扩张导致盲肠肠扭转的发展。我们建议对于进行性腹胀并伴有神经发育迟缓和便秘病史的患者,应考虑盲肠和近端大肠肠扭转。

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