剖宫产术后Ogilvie综合征一例报告

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Galician Medical Journal Pub Date : 2021-06-01 DOI:10.21802/GMJ.2021.2.6
S. Sninate, H. Bellamlih, S. Allioui, L. Jroundi, F. Laamrani
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引用次数: 0

摘要

背景。奥吉维综合征是一种罕见的产后并发症。它的特点是急性结肠假性梗阻,发生在没有机械原因。早期诊断对避免盲肠穿孔至关重要。病例报告。我们报告一例39岁女性(妊娠期2,第2段)剖宫产后出现Ogilvie综合征,10年前因输卵管狭窄和浆膜下纤维瘤继发性不孕症,导致妊娠39周第二次妊娠剖宫产指征。剖宫产术后3天,患者出现明显腹胀、压痛、呕吐、虚弱、恶心;腹部x光片显示盲肠膨胀。腹部计算机断层扫描和静脉造影剂显示升结肠和横结肠膨胀伴气液水平,但无过渡性机械阻塞。病人得到了成功的治疗。结论。奥吉维综合征是一种罕见但严重的并发症,在健康的年轻患者中,剖宫产后出现疼痛、严重腹胀和排气失败应予以考虑。
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Ogilvie Syndrome Following Caesarean Section: A Case Report
Background. Ogilvie syndrome is a rare postpartum complication. It is characterized by an acute colonic pseudo-obstruction which occurs in the absence of a mechanical cause. Early detection of the diagnosis is essential to avoid cecal perforation. Case report. We report a case of Ogilvie syndrome following caesarean section in a 39-year-old woman (gravida 2, para 2) with a history of secondary infertility 10 years ago due to tubal stenosis and subserous fibroma, which led to the indication for cesarean section in second pregnancy at 39 weeks of gestation. Three days after cesarean section, the patient presented with significant abdominal distension and tenderness, vomiting, weakness, and nausea; an abdominal X-ray showed cecal distension. Abdominal computed tomography scan with intravenous contrast revealed distension of the ascending and transverse colon with air-fluid levels but without transitional mechanical obstruction. The patient was successfully treated. Conclusions. Ogilvie syndrome is a rare but serious complication that should be considered in fit young patients who present with pain, severe abdominal distension and failure to pass flatus after caesarean section.
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