Presence of Chorionic Villi Does Not Exclude Choriocarcinoma: A Case Report of Early Choriocarcinoma Associated with a Complete Hydatidiform Mole
Background: Gestational choriocarcinoma is a highly aggressive trophoblastic neoplasm. Historically, the presence of chorionic villi was considered discordant with the diagnosis of choriocarcinoma. We report a case of early gestational choriocarcinoma arising in a post-molar setting with residual chorionic villi, creating a diagnostic pitfall. Case report: a 51-year-old woman with a prior complete hydatidiform mole showed plateauing β-human chorionic gonadotropin (ß-hCG) levels. She underwent total laparoscopic hysterectomy. Histologic examination of the uterine mass revealed a malignant biphasic-to-triphasic trophoblastic proliferation with marked atypia, brisk mitotic activity, extensive hemorrhage, and necrosis, situated immediately adjacent to a single residual molar villus. Immunohistochemistry showed strong β-human chorionic gonadotropin expression in syncytiotrophoblasts, a elevated Ki-67 index (∼80%), focal human placental lactogen (hpL) expression, and absence of p63 staining, confirming choriocarcinoma and excluding other trophoblastic tumors. Conclusion: this case demonstrates that the presence of chorionic villi does not exclude a diagnosis of choriocarcinoma and underscores the necessity of rigorous clinicopathologic correlation.
Authors
- Stephanie Barak (ORCID: https://orcid.org/0000-0003-3966-1263)
- Kostadinov S.
- Shah J.
Institutions
- Brown University (US)
- Women & Infants Hospital of Rhode Island (US)
Publication Details
- Journal
- Fetal and Pediatric Pathology
- Published
- 2026-09-25
- DOI
- https://doi.org/10.1080/15513815.2026.2735832
- Primary Topic
- Gestational Trophoblastic Disease Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00