...
首页> 外文期刊>Eastern Journal of Medicine >A case of rectal villous adenoma in a 28 year old female patient presenting with Depletion syndrome
【24h】

A case of rectal villous adenoma in a 28 year old female patient presenting with Depletion syndrome

机译:一位患有耗竭综合征的28岁女性患者的直肠绒毛状腺瘤一例

获取原文
   

获取外文期刊封面封底 >>

       

摘要

A case of rectal villous adenoma in a 28 year old female patient presenting with Depletion syndrome Sheref A. Elseidy 1, Haitham H. Alzamli1, Ahmed A. Abd Alkader2, Esraa Mamdouh1, Marina S. Ghaly1 1Sheref A. Elseidy,Haitham H. Alzamli,Esraa Mamdouh,Marina S. Ghaly: Department of Internal medicine, Ain Shams University, Cairo, Egypt 2Ahmed A. Abd Alkader: Department of rheumatology, Ain Shams University, Cairo, Egypt BACKGROUND: Secretory villous adenoma is one of the rare causes of severe secretory diarrhea,acute kidney injury and refractory electrolyte imbalance.A classic triad named McKittrick-Wheelock syndrome.aggressive hydroelectrolyte rebalancing is often needed, and curative treatment is obtained only with complete removal of the lesion, by endoscopic resection or surgery. High clinical suspicion in patients with severe dehydration due secretory diarrhea and concomitant electrolyte imbalance is both mandatory and essential for early diagnosis and treatment before complications arise. case presentation: In this case we describe a 28 year old female patient suffering from 6 months of secretory diarrhea, presented to our emergency department with severe dehydration, acute renal failure, hyponatremia and hypokalemia After re hydration and electrolyte replacement confirmation of the diagnosis was done by colonoscopy and biopsy showing 3 sessile colonic polyps (2 at distal end of Transverse colon, largest one at descending colon) the biopsy confirmed the presence of villous adenoma with high grade dysplasia. Normalization of the electrolyte imbalance and the kidney functions was done and she was successfully treated with surgical resection that lead to complete resolution of symptoms. conclusion: McKittrick-Wheelock syndrome is a rare life threatening depletion syndrome that can lead to acute kidney injury and electrolyte imbalance with concomitant organ damage. Early management by vigorous repletion therapy and curative surgical resection will mostly resolve the symptoms and complications.
机译:一名患有消耗综合征的28岁女性患者的直肠绒毛状腺瘤病例Sheref A.Elseidy 1,Haitham H.Alzamli1,Ahmed A.Abd Alkader2,Esraa Mamdouh1,Marina S.Ghaly1 1 Sheref A.Elseidy,Haitham H.Alzamli ,Esraa Mamdouh,Marina S. Ghaly:埃及开罗艾因沙姆斯大学内科2 Ahmed A. Abd Alkader:埃及开罗艾因沙姆斯大学风湿科严重的分泌性腹泻,急性肾损伤和难治性电解质失衡。一个名为McKittrick-Wheelock综合征的经典三联征。经常需要进行激进的电解质修复,只有通过彻底切除病灶,通过内窥镜切除术或手术才能获得治愈。由于分泌性腹泻而导致严重脱水的严重临床怀疑和伴随的电解质失衡,对于在并发症发生之前进行早期诊断和治疗既是必不可少的,也是必不可少的。病例介绍:在本例中,我们描述了一位患有6个月分泌性腹泻的28岁女性患者,该患者因严重脱水,急性肾功能衰竭,低钠血症和低钾血症出现在我们的急诊科,在补液和补充电解质后确认了诊断通过结肠镜检查和活检显示3例无固定性结肠息肉(横结肠远端2个,降结肠最大1个),活检证实存在高度不典型增生的绒毛状腺瘤。电解质失衡和肾功能正常化,她成功地接受了手术切除,导致症状完全缓解。结论:McKittrick-Wheelock综合征是一种罕见的威胁生命的耗竭综合征,可导致急性肾损伤和电解质紊乱,并伴有器官损害。大力补充疗法和根治性手术切除的早期治疗将在很大程度上解决症状和并发症。

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