Recurrent Complete Hydatidiform Mole with Increased Myometrial Vascularity: A Case Report

Kumkum Singh

King George’s Medical University, Lucknow, Uttar Pradesh, India.

Suman Lata *

Department of Obstetrics and Gynecology, King George’s Medical University, Lucknow, Uttar Pradesh, India.

Tanima Verma

Department of Obstetrics and Gynecology, King George’s Medical University, Lucknow, Uttar Pradesh, India.

*Author to whom correspondence should be addressed.


Abstract

Background: Recurrent complete hydatidiform mole is uncommon, and marked myometrial vascularity may complicate uterine evacuation because of haemorrhage risk.

Case Presentation: A 28-year-old multiparous woman (P1+2, L1) presented following a previous pregnancy evacuation in Nepal, persistent amenorrhoea, vomiting, and abnormal ultrasonographic findings. Imaging demonstrated a markedly enlarged uterus containing a heterogeneous echogenic mass with multiple irregular cystic areas, together with markedly increased myometrial vascularity and arteriovenous malformations predominantly in the fundoposterior region. Serum β-hCG was 1154 mIU/mL and haemoglobin was 11.0 g/dL. The patient was stabilised, blood was cross-matched, and suction dilatation and evacuation was performed under ultrasound guidance. She subsequently received one 8-day methotrexate–leucovorin cycle. Histopathological examination demonstrated diffuse hydropic swelling of chorionic villi with circumferential trophoblastic proliferation and absence of fetal tissue; p57 immunostaining was negative, confirming complete hydatidiform mole. Following evacuation, vomiting and systemic symptoms resolved within 48 hours and haemodynamic stability was maintained. Serial β-hCG monitoring showed a decline from 1154 mIU/mL to 150 mIU/mL at 8 weeks, with continued downward progression.

Conclusion: This case highlights the importance of recognising recurrent molar pregnancy, evaluating marked uterine vascularity before intervention, obtaining histopathological confirmation, and maintaining structured β-hCG surveillance after treatment. Careful follow-up remained necessary throughout the documented post-treatment surveillance period.

Keywords: Recurrent complete hydatidiform mole, gestational trophoblastic disease, myometrial vascularity, arteriovenous malformation, β-hCG, methotrexate


How to Cite

Singh, Kumkum, Suman Lata, and Tanima Verma. 2026. “Recurrent Complete Hydatidiform Mole With Increased Myometrial Vascularity: A Case Report”. Asian Research Journal of Gynaecology and Obstetrics 9 (1):649-56. https://doi.org/10.9734/arjgo/2026/v9i1371.

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