Suppr超能文献

罕见病例报告:双胎妊娠中完全性葡萄胎与正常胎儿并存

Rare Case Report: Coexistence of Complete Hydatidiform Mole and Normal Fetus in a Twin Pregnancy.

作者信息

Li Ping, Liu XiuPing

机构信息

Obstetrics and Gynecology Department of the Hebei Medical University Third Hospital, Shijiazhuang, People's Republic of China.

出版信息

Int J Womens Health. 2025 Apr 28;17:1175-1181. doi: 10.2147/IJWH.S510609. eCollection 2025.

Abstract

BACKGROUND

The coexistence of a complete hydatidiform mole with a normal fetus in a twin pregnancy is a rare, high-risk obstetric condition with an extremely low incidence rate, presenting numerous clinical management challenges. The rarity of such cases, coupled with the scarcity of comprehensive literature, makes the successful management of this case a source of valuable experience and novel insights for clinical practice.

CASE PRESENTATION

A 32-year-old patient conceived following a clomiphene-induced ovulation regimen. Mid-pregnancy ultrasound indicated a twin pregnancy (one viable fetus, the other consistent with the appearance of a complete hydatidiform mole), and the patient chose to continue the pregnancy. At 36+4 weeks of gestation, the patient was admitted for pregnancy-induced hypertension and underwent a cesarean section, delivering a healthy female infant and simultaneously removing the molar tissue. Postoperative pathological examination confirmed a complete hydatidiform mole with invasive lesions, which progressed to an invasive hydatidiform mole. The patient underwent seven cycles of methotrexate combination chemotherapy, with a follow-up period of three years showing no recurrence, ensuring the health of both mother and child.

CONCLUSION

Managing twin gestations involving a complete hydatidiform mole and a normal fetus necessitates a multidisciplinary approach, grounded in individualized assessment. The successful treatment of this case demonstrates that standardized diagnosis, close postoperative follow-up, and chemotherapy are crucial factors in improving maternal and fetal outcomes, offering significant clinical reference value.

摘要

背景

双胎妊娠中完全性葡萄胎与正常胎儿并存是一种罕见的、高风险的产科情况,发病率极低,带来了众多临床管理挑战。此类病例的罕见性,再加上全面文献的稀缺,使得成功处理该病例成为临床实践中宝贵经验和新见解的来源。

病例报告

一名32岁患者在克罗米芬诱导排卵方案后受孕。孕中期超声显示双胎妊娠(一个胎儿存活,另一个符合完全性葡萄胎表现),患者选择继续妊娠。妊娠36 + 4周时,患者因妊娠高血压入院并接受剖宫产,产下一名健康女婴,同时切除葡萄胎组织。术后病理检查证实为伴有浸润性病变的完全性葡萄胎,进展为侵蚀性葡萄胎。患者接受了七个周期的甲氨蝶呤联合化疗,随访三年无复发,确保了母婴健康。

结论

处理涉及完全性葡萄胎和正常胎儿的双胎妊娠需要多学科方法,基于个体化评估。该病例的成功治疗表明,标准化诊断、术后密切随访和化疗是改善母婴结局的关键因素,具有重要的临床参考价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b0/12047649/4ee46d1b4c89/IJWH-17-1175-g0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验