Alnasarat Ahmad, Elrazzaz Mostafa, Manasrah Nouraldeen
College of Osteopathic Medicine, Michigan State University, Lansing, Michigan, USA.
Department of Internal Medicine, Detroit Medical Center (Sinai Grace), Wayne State University, Detroit, Michigan, USA.
Case Rep Gastrointest Med. 2024 Dec 14;2024:5378390. doi: 10.1155/crgm/5378390. eCollection 2024.
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. 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. 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.
急性结肠假性梗阻(ACPO),即奥吉尔维综合征,是一种罕见病症,其特征为结肠显著扩张但无机械性梗阻。症状包括腹痛、腹胀、恶心、呕吐以及无法排气或排便。虽然该病在60岁以上男性中较为常见,但我们报告了一例具有挑战性的病例,患者为一名44岁的非洲男性,反复出现腹胀和不适。最终,他在接受多种治疗方式后病情有所改善,这凸显了奥吉尔维综合征治疗的复杂性。一名在美国的44岁尼日利亚男性,患有高血压且有严重酒精使用障碍,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。初步诊断表明是低钾血症和脱水导致的代谢性脑病。尽管进行了积极治疗,他仍出现了严重的腹胀和便秘。CT扫描显示结肠弥漫性扩张,小肠未见正常。保守治疗措施失败,因此需要转入重症监护病房、接受全胃肠外营养(TPN)并使用经验性抗生素。尽管最初对结肠镜减压有反应,但患者病情复发。新斯的明显著改善了他的病情,使其完全康复并出院。 这个具有挑战性的病例凸显了奥吉尔维综合征治疗的复杂性以及早期识别和逐步治疗方法的重要性。采用以患者为中心的计划,利用保守措施、药物和内镜干预对于改善这些病例的治疗结果至关重要。