Pathogenesis and symptom of early hemorrhage in extrafollicular ovarian pregnancy onset at 4weeks gestation: A case report

妊娠4周时发生卵泡外卵巢妊娠早期出血的发病机制及症状:病例报告

阅读:1

Abstract

INTRODUCTION: Ovarian pregnancy is a rare form of ectopic pregnancy, accounting for approximately 3 % of cases, with an incidence ranging from 1 in 2100 to 1 in 7000 pregnancies. Its diagnosis is challenging due to nonspecific symptoms and difficulty distinguishing it from corpus luteum cysts or tubal pregnancies. Delayed recognition can lead to life-threatening hemorrhage. PRESENTATION OF CASE: A 34-year-old gravida 3 para 3 Japanese woman presented with acute abdominal pain and hypovolemic shock 33 days after her last menstrual period. Imaging revealed a right ovarian cystic mass, intra-abdominal bleeding, and an empty uterus. Emergency laparoscopy identified a 5-mm gestational sac-like lesion on the right ovary. Laparoscopic wedge resection was performed. Pathological analysis confirmed extravillous trophoblast invasion into ovarian stromal vessels. A corpus luteum was observed at a separate location, supporting the diagnosis of secondary extrafollicular ovarian pregnancy. The patient recovered uneventfully. DISCUSSION: Ovarian pregnancies are classified as primary or secondary, and intrafollicular or extrafollicular. This case demonstrated secondary extrafollicular implantation with vascular invasion. Updated diagnostic criteria emphasize intact fallopian tubes, hemorrhagic ovarian lesions, and pregnancy tissue identification. Early detection remains difficult, particularly before 5 weeks gestation, and diagnosis often requires surgical and pathological confirmation. CONCLUSION: This case underscores the importance of early recognition and laparoscopic management of ovarian pregnancy. Pathological findings aid in understanding implantation mechanisms and differentiating from similar adnexal conditions. Minimally invasive surgery enabled successful hemostasis and fertility preservation. Improved clinical awareness is essential to reduce complications associated with this rare condition.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。