Transverse-Sigmoid Colon Synchronous Volvulus in a Patient with Lennox-Gastaut Syndrome: Case Report

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Abstract

Introduction: Lennox-Gastaut syndrome (LSG) is an epileptic encephalopathy characterized by a triad: 1). tonic seizures during sleep with atonic and atypical absence seizures, 2). cognitive and 3). behavioral It is estimated that SLG affects between 1 to 2% of patients with epilepsy. In general, LGS often occurs in young children. The etiology of LGS can be classified as cryptogenic or symptomatic. Symptomatic etiology of LGS can be secondary to hypoxic ischemic encephalopathy, congenital brain malformation, vascular malformation, genetics (tuberous sclerosis), trauma, brain tumor, or perinatal meningoencephalitis. Clinical Case: This is a 29-year-old woman, who has a significant history of prolonged prostration; severe cognitive disorder, Lennox-Gastaut syndrome since childhood. She was admitted to the emergency department with symptoms of abdominal distension of seven days of evolution and generalized pain in all abdominal quadrants. A simple computed tomography of the abdomen was performed, where distension of bowel loops was observed at the expense of mesenteric torsion with data of colonic volvulus with little free fluid. It is evaluated by the general surgery service who determines emergency surgical management by means of exploratory laparotomy, the following findings are addressed and obtained: toxic megacolon from the left end of the transverse colon to the middle third of the sigmoid colon, with multiple necrotic patches, as well as volvulus of the transverse and sigmoid colon, proceeding to perform a left hemicolectomy with colostomy of the transverse colon. Discussion: In children, the incidence is estimated at 2 per 100,000, and it is common in men. LGS is one of the most commonly encountered drug-resistant epileptic encephalopathies, with mortality rates ranging from 3-7%. There are many treatment options for these patients, such as antiepileptic drugs, ketogenic diets, VNS therapy (vagus nerve stimulation) callosotomy, and resective epilepsy surgery.
横乙状结肠同步扭转1例lenox - gastaut综合征
lenox - gastaut综合征(LSG)是一种癫痫性脑病,其特征为:1)睡眠时强直性发作伴失张力和非典型失神发作,2)认知和3)行为。据估计,1%至2%的癫痫患者受SLG影响。一般来说,LGS常发生在幼儿身上。LGS的病因可分为隐源性和症状性。LGS的症状性病因可能继发于缺氧缺血性脑病、先天性脑畸形、血管畸形、遗传(结节性硬化症)、创伤、脑肿瘤或围产期脑膜脑炎。临床病例:这是一名29岁的女性,她有明显的长期萎靡病史;严重的认知障碍,从小就有lenox - gastaut综合征。她因腹胀症状持续7天,腹部各象限全身疼痛而住进急诊科。对腹部进行简单的计算机断层扫描,观察到肠袢扩张,肠系膜扭转,结肠扭转伴少量游离液体。通过剖腹探查确定紧急手术处理的普通外科部门对其进行了评估,并得到了以下发现:横结肠左端至乙状结肠中间三分之一处有毒性巨结肠,有多个坏死斑块,以及横结肠和乙状结肠扭转,继续进行左结肠切除术和横结肠造口术。讨论:在儿童中,发病率估计为10万分之2,在男性中也很常见。LGS是最常见的耐药癫痫性脑病之一,死亡率在3-7%之间。这些患者有许多治疗选择,如抗癫痫药物,生酮饮食,VNS治疗(迷走神经刺激)胼胝体切开术和切除癫痫手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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