Monish Gupta, Harshada Rajendra Bhangale
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Introduction: Placental Site Trophoblastic Tumor (PSTT) is a rare and distinct subtype of gestational trophoblastic neoplasia (GTN), arising from intermediate trophoblasts. Representing only 0.23% to 3% of GTD cases globally, PSTT is typically confined to the uterine implantation site.1 Ectopic localization of PSTT, particularly within the fallopian tube, is exceedingly rare, with approximately 20 cases reported in the published literature to date.3 This tumor presents a unique diagnostic challenge as its low production of human chorionic gonadotropin (betahCG) often contradicts standard diagnostic algorithms used for ectopic pregnancy, risking inappropriate conservative management.
Case Presentation: A 32-year-old G2P1 patient presented with 6 weeks of amenorrhea, mild vaginal bleeding, and unilateral lower abdominal pain. Initial quantitative serum beta-hCG was 850 IU/L, with a suboptimal rise over 48 hours. Transvaginal ultrasound confirmed the absence of an intrauterine pregnancy (IUP) and identified a complex, highly vascularized mass (3.5 cm) in the right adnexa, necessitating laparoscopic right salpingectomy. Initial histopathology demonstrated an invasive trophoblastic proliferation. Definitive diagnosis of PSTT was established through immunohistochemistry (IHC), characterized by strong, diffuse positivity for Human Placental Lactogen (hPL), focal positivity for betahCG, and a low proliferative index (Ki-67: 15%)
Management: The patient was staged as FIGO Stage I (localized disease). Given the localized nature and favorable prognostic factors (low mitotic rate, short interval since antecedent pregnancy), adjuvant chemotherapy was avoided. The patient was placed on a rigorous follow-up protocol involving long-term surveillance with periodic imaging (MRI) and monitoring of $\beta$-hCG and hPL, acknowledging the limitations of hCG monitoring alone for PSTT.
Conclusion: Ectopic PSTT is an ultra-rare malignancy whose clinical presentation is misleading due to low $\beta$-hCG production, challenging timely preoperative diagnosis.6 Definitive diagnosis hinges entirely on specialized pathological examination and IHC studies. While salpingectomy can be curative for localized, low-risk disease, specialized, long-term surveillance is mandatory to detect potential late recurrence, emphasizing the necessity of reporting such cases to inform international management guidelines.7
Bhangale HR, Gupta M. Placental Site Trophoblastic Tumor Originating in Tubal Ectopic Pregnancy: An Extremely Rare Case Report and Crucial Management Dilemma. Ind Jr of Path: Res and Practice. 2026;15(1):85-90.
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| Received | Accepted | Published |
|---|---|---|
| December 17, 2025 | January 20, 2026 | April 30, 2026 |
Wednesday 17 June 2026, 15:04:20 (IST)
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| Received | December 17, 2025 |
| Accepted | January 20, 2026 |
| Published | April 30, 2026 |
This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.