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HELLP 综合征剖宫产术后并发急性结肠假性梗阻并肠破裂:一例报告。

Acute colonic pseudo-obstruction with bowel rupture after caesarean section in HELLP syndrome: a case report.

机构信息

Department of Obstetrics and Gynaecology, First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, 17, Lu Jiang Road, Hefei, 230001, Anhui, P. R. China.

出版信息

BMC Pregnancy Childbirth. 2020 Nov 25;20(1):727. doi: 10.1186/s12884-020-03414-9.

Abstract

BACKGROUND

Ogilvie syndrome, also known as acute colonic pseudo-obstruction (ACPO), can occur postpartum after caesarean section (C-section), often resulting in caecal dilatation. The incidence rate is approximately 100 cases in 100,000 patients per year (Ross et al., Am Surg 82:102-11, 2016). Without proper diagnosis and treatment, it may progress to intestinal perforation or other fatal complications.

CASE PRESENTATION

A 39-year-old pregnant woman underwent emergency low-segment C-section due to complications of Haemolysis, Elevated Liver enzymes and Low Platelets syndrome (HELLP) syndrome. ACPO was suspected on the third day after C-section based on inability to pass flatus, evident abdominal distension, slight abdominal pain, and computed tomography (CT) scan revealing severe, diffuse colonic distention with caecal dilatation of approximately 9 cm. Based on these findings, conservative treatment was implemented. However, 6 days after C-section, her symptoms worsened, and CT showed possible intestinal perforation; thus, an emergency laparotomy was performed. Due to a 3-cm (diameter) laceration in the anterolateral wall of the ascending colon and a 5-cm tear in the ileocecal junction, in combination with mucosal eversion in the colon, resection of the ileocecum, distal closure of the ascending colon, and a terminal ileostomy were performed. The patient was discharged 2 weeks post-laparotomy and continued to undergo nursing care for the incision and stoma. Ileostomy was performed 4 months later.

CONCLUSION

Ogilvie syndrome after C-section is an extremely rare but severe condition, which warrants early recognition and treatment to prevent potentially fatal complications, especially in patients with poor health status.

摘要

背景

奥格尔维氏综合征,又称急性结肠假性梗阻(ACPO),可在剖宫产(C -section)后产后发生,常导致盲肠扩张。发病率约为每年每 100,000 例患者中有 100 例(Ross 等人,Am Surg 82:102-11, 2016)。如果没有适当的诊断和治疗,它可能会发展为肠穿孔或其他致命并发症。

病例介绍

一位 39 岁的孕妇因溶血性肝酶升高和血小板减少综合征(HELLP)综合征并发症而行急诊下段剖宫产。在剖宫产术后第三天,由于不能排气、明显腹胀、轻度腹痛,并进行计算机断层扫描(CT)扫描显示严重弥漫性结肠扩张,盲肠扩张约 9cm,怀疑发生 ACPO。根据这些发现,进行了保守治疗。然而,在剖宫产术后 6 天,她的症状恶化,CT 显示可能发生肠穿孔;因此,进行了紧急剖腹手术。由于升结肠前外侧壁有 3cm(直径)的裂伤和回盲部有 5cm 的撕裂,加上结肠黏膜外翻,进行了回盲部切除、升结肠远端关闭和末端回肠造口术。患者在剖腹手术后 2 周出院,并继续接受切口和造口护理。4 个月后进行了回肠造口术。

结论

C -section 后奥格尔维氏综合征是一种极其罕见但严重的疾病,需要早期识别和治疗,以预防潜在的致命并发症,特别是在健康状况不佳的患者中。

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