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病例报告:原发性网膜妊娠的多学科管理,包括术中超声检查

Case Report: Multidisciplinary management of primary omental pregnancy involving intraoperative ultrasound.

作者信息

Wang Shanshan, Shao Huaguo, Huang Yan, Li Yanqing, Feng Ting, Pan Lin

机构信息

Department of Ultrasound, Hangzhou Xixi Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China.

Institute of Hepatology and Epidemiology, Hangzhou Xixi Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China.

出版信息

Front Med (Lausanne). 2025 Aug 7;12:1571248. doi: 10.3389/fmed.2025.1571248. eCollection 2025.

Abstract

INTRODUCTION

Primary omental pregnancy (OP) is very rare, and achieving an accurate diagnosis has always been a challenge for obstetricians, gynecologists, and sonographers. Our attempt to utilize intraoperative ultrasonography has facilitated a definitive diagnosis for masses lacking obvious purple or blue characteristics under observation. This approach could provide a solution for challenges faced in intraoperative diagnosis.

CASE PRESENTATION

We present the case of an 18-year-old woman who was 5 months postpartum and presented with intermittent lower abdominal pain for 3 days with no obvious causes. Emergency ultrasonography diagnosed an abdominal pregnancy (AP) with abdominal and pelvic hemorrhage. Laparoscopic surgery revealed a mass on the omentum, but the surface lacked the typical purple-blue appearance. Intraoperative ultrasonography was employed, and the suspicious omental mass was shifted to the left pelvic wall. Under ultrasound guidance, the echo of a gestational sac (GS) was observed within the mass. The AP tissue and a portion of the omentum were resected. Examination of the resected omental specimen revealed chorionic villi tissue. The diagnosis was confirmed as primary OP. The operations were successful, and the patient recovered well postoperatively.

CONCLUSION

Due to early detection, the patient received timely treatment, which played a crucial role in selecting the therapeutic plan. Chronic pelvic inflammatory disease (PID) was identified intraoperatively, suggesting that it may be a potential risk factor for OP. It is imperative for us to gain a deeper understanding of the diagnosis of primary OP, analyze its potential precipitating factors, and expand the scope of ultrasonographic examination by searching for a GS in other locations when none is visualized within the uterine cavity.

摘要

引言

原发性网膜妊娠(OP)非常罕见,对产科医生、妇科医生和超声检查人员来说,做出准确诊断一直是一项挑战。我们尝试使用术中超声检查,为观察中缺乏明显紫蓝色特征的肿块做出明确诊断提供了便利。这种方法可以解决术中诊断面临的挑战。

病例报告

我们报告一例18岁产后5个月的女性病例,她无明显诱因出现下腹部间歇性疼痛3天。急诊超声检查诊断为腹腔妊娠(AP)伴腹腔和盆腔出血。腹腔镜手术发现网膜上有一个肿块,但表面缺乏典型的紫蓝色外观。采用术中超声检查,将可疑的网膜肿块移至左盆腔壁。在超声引导下,在肿块内观察到妊娠囊(GS)的回声。切除了AP组织和部分网膜。对切除的网膜标本进行检查,发现有绒毛膜绒毛组织。确诊为原发性OP。手术成功,患者术后恢复良好。

结论

由于早期发现,患者得到了及时治疗,这对选择治疗方案起到了关键作用。术中发现慢性盆腔炎(PID),提示其可能是OP的潜在危险因素。我们必须更深入地了解原发性OP的诊断,分析其潜在的诱发因素,并在宫腔内未发现GS时,通过在其他部位寻找GS来扩大超声检查的范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ee0/12368590/28d302bd7661/fmed-12-1571248-g001.jpg

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