A Challenging Case of Recurrent Ogilvie Syndrome: Exploring Causes and Treatment Modalities.

IF 0.6 Q4 GASTROENTEROLOGY & HEPATOLOGY
Case Reports in Gastrointestinal Medicine Pub Date : 2024-12-14 eCollection Date: 2024-01-01 DOI:10.1155/crgm/5378390
Ahmad Alnasarat, Mostafa Elrazzaz, Nouraldeen Manasrah
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引用次数: 0

Abstract

Introduction: Acute colonic pseudo-obstruction (ACPO), or Ogilvie syndrome, is a rare condition marked by significant colon distention without mechanical obstruction. Symptoms include abdominal pain, bloating, nausea, vomiting, and an inability to pass gas or stool. Although common in males over 60, we report a challenging case of a 44-year-old man from Africa with recurrent abdominal distention and discomfort. Ultimately, he improved after receiving multiple treatment modalities, highlighting the complexities of Ogilvie syndrome management. Case Presentation: A 44-year-old Nigerian male in the United States with hypertension and significant alcohol use disorder presented with altered mental status and bilateral lower extremity weakness after fasting and hydrochlorothiazide abuse. Initial diagnostics indicated metabolic encephalopathy from hypokalemia and dehydration. Despite aggressive treatment, he developed severe abdominal distension and obstipation. A CT scan showed diffuse colonic dilatation without a normal small bowel. Conservative measures failed, necessitating ICU transfer, TPN, and empiric antibiotics. Despite an initial response to colonoscopy decompression, the patient experienced recurrence. Neostigmine significantly improved his condition, leading to full recovery and discharge. Conclusion: This challenging case highlights the complexities of managing Ogilvie syndrome and the importance of early identification and a stepwise approach to treatment. Incorporating a patient-centered plan utilizing conservative measures, pharmacological agents and endoscopic interventions are essential for improving outcomes in these cases.

一个具有挑战性的病例复发奥吉维综合征:探讨原因和治疗方式。
简介:急性结肠假性梗阻(ACPO)或Ogilvie综合征是一种罕见的疾病,其特征是明显的结肠扩张而没有机械阻塞。症状包括腹痛、腹胀、恶心、呕吐、不能排便或排气。虽然常见于60岁以上的男性,但我们报告了一个来自非洲的44岁男性复发性腹胀和不适的挑战性病例。最终,在接受多种治疗方式后,他的病情有所好转,这凸显了奥吉维综合征治疗的复杂性。病例介绍:美国一名44岁尼日利亚男性,患有高血压和明显的酒精使用障碍,在禁食和滥用氢氯噻嗪后出现精神状态改变和双侧下肢无力。初步诊断为低钾血症和脱水引起的代谢性脑病。尽管进行了积极的治疗,他还是出现了严重的腹胀和便秘。CT扫描显示弥漫性结肠扩张,没有正常的小肠。保守措施失败,需要转入ICU, TPN和经验性抗生素。尽管最初对结肠镜减压有反应,但患者经历了复发。新斯的明显著改善了他的病情,使他完全康复出院。结论:这个具有挑战性的病例强调了管理奥吉维综合征的复杂性,以及早期识别和逐步治疗的重要性。结合以患者为中心的计划,采用保守措施,药物和内镜干预是改善这些病例结果的必要条件。
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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来源期刊
Case Reports in Gastrointestinal Medicine
Case Reports in Gastrointestinal Medicine GASTROENTEROLOGY & HEPATOLOGY-
自引率
0.00%
发文量
33
审稿时长
14 weeks
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