首页> 外文期刊>Cureus. >Giant Mucocele of the Remnant Esophagus: Case Report of a Rare Complication Following a Bipolar Esophageal Exclusion Procedure
【24h】

Giant Mucocele of the Remnant Esophagus: Case Report of a Rare Complication Following a Bipolar Esophageal Exclusion Procedure

机译:残余食管的巨型粘膜:案例报告对双极食管排除程序后罕见的并发症

获取原文
           

摘要

We describe a case of a symptomatic mucocele of the esophagus following surgical isolation of the diseased esophagus, which needed surgical resection. A 33-year-old male presented to us with shock, high-grade fever, and breathlessness five days after the onset of sudden, severe lower chest and upper abdominal pain preceded by an episode of retching and vomiting. He was initially managed elsewhere by right intercostal drainage for right-sided pleural effusion, broad-spectrum parenteral antibiotics, and total parenteral nutrition. CT chest showed a right loculated pleural effusion and distal oesophageal perforation with active contrast leak into the right pleural space. He was subsequently referred to us in view of suspected Boerhaave’s syndrome and clinical worsening. In view of hemodynamic instability with uncontrolled sepsis, he was planned for surgery. Intraoperatively, there was a 4 cm long distal oesophageal perforation, 4 cm above the esophagogastric junction on the right, with an unhealthy apex, communicating with a large abscess cavity in the right pleural space with thick purulent contents. End cervical esophagostomy with esophagogastric junction stapling and feeding jejunostomy was performed in addition to transhiatal drainage of the abscess at the lower end of the esophagus and the placement of an?additional intercostal drain. The postoperative period was uneventful, and he was discharged. After two months, he was assessed for possible esophagectomy and gastric pullup. Dense adhesions at thoracoscopy precluded any esophageal delineation and dissection. Attempted transhiatal dissection of the esophagus was unsuccessful in view of cicatrization, and it was decided to forego esophagectomy and proceed with bypass alone by a retrosternal gastric pull-up and cervical esophagogastrostomy. He was discharged following an uneventful postoperative period of recovery. Three months later, the patient presented with complaints of pain in the chest for three weeks, associated with hiccups. He was diagnosed to have a mucocele of the remnant esophagus based on a CT scan. The esophageal mucocele was excised by a transthoracic approach and, he was relieved of the pressure symptoms. Following the esophageal exclusion procedure, a mucocele of the remnant esophagus can develop due to the accumulation of secretions leading to subsequent dilatation. Small mucoceles are usually asymptomatic and often go unnoticed. However, in rare cases, it may enlarge to cause compression symptoms such as respiratory distress, chest pain, cough, hiccups, and an inability to swallow. Cross-sectional imaging clinches the diagnosis, and definitive surgery consists of surgical resection by a transthoracic approach.
机译:我们描述了患病食管外科手术分离后食道症状的症状的案例,这需要手术切除。一名33岁的男性在休息,高年级的发烧和呼吸呼吸困难后,突然,严重的下胸和上腹部疼痛前五天呈现给我们,前腹部疼痛,前腹部疼痛在复合和呕吐。他最初在右侧肋间流量,广谱肠胃外抗生素和全肠外营养总体抗冲击引流的其他地方在其他地方进行管理。 CT胸部显示出正确的胸腔积液和远端食管穿孔,具有积极对比泄漏到右侧胸腔空间。鉴于怀疑的Boerhaave综合征和临床恶化,他随后提到了美国。考虑到血流动力学不稳定与不受控制的败血症,他计划进行手术。术中,在右侧的食管胃部结4厘米的远端卵囊穿孔,4厘米处,具有不健康的顶点,与右胸腔空间中的大脓肿腔进行沟通,具有厚的脓性内容物。除了在食道下端的脓肿的转骨引流和放置腹静脉排放的脓肿和放置之外,还进行了对食管胃部结吻合和饲喂的颈部食管术。术后期间是不行的,他被解雇了。两个月后,他被评估了可能的食道切除术和胃部上拉。胸腔镜检查的致密粘连绝不能进行食管描绘和解剖。考虑到食道的试图转骨剖检鉴于Cicatrization,食道不成功,并决定前食管切除术,并通过胸膜胃上拉和宫颈食管瘤术进行旁路。他在一个不确定的术后恢复期间出院。三个月后,患者患有胸部疼痛的抱怨三周,与打嗝相关。他被诊断为基于CT扫描的残余食道具有粘膜胶囊。食管粘膜胶凝由经晶态方法切除,他解除了压力症状。在食管排除过程之后,由于分泌物的积累导致随后扩张,可以发育不遗留食管的粘液泡。小粘膜通常是无症状的,经常被忽视。然而,在极少数情况下,它可能会扩大,导致呼吸窘迫,胸痛,咳嗽,打嗝等压缩症状和无法吞咽。横截面成像诱使诊断,明确的手术由经过触发方法进行手术切除。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号