Evidence map›Paper›PMID 41491402›Full record

ArticleThe American journal of surgical pathology2026

Primary Uterine Nongestational Placental Site Trophoblastic Tumor as a Distinct Entity: A Report of 5 Cases.

Alexis Trecourt, Geoffrey J Maher, Rosemary A Fisher, Katie McDonald, Michael J Seckl, Matthew C Winter, Snezana Susnjar, Vesna Kesić, Pierre Descargues, Mojgan Devouassoux-Shisheboran and 2 more

Abstract readCase Reports
In one paragraph

Article in The American journal of surgical pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Alexis TrecourtHospices Civils de Lyon, Centre Hospitalier Lyon-Sud, Service de Pathologie Multi-Site, Pierre Bénite.
Geoffrey J MaherTrophoblastic Tumour Screening & Treatment Centre, Imperial College NHS Trust, Charing Cross Hospital.
Rosemary A FisherDepartment of Surgery and Cancer, Imperial College London, Charing Cross Hospital, London.
Katie McDonaldSheffield Centre for Trophoblastic Disease, Weston Park Cancer Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield.
Michael J SecklTrophoblastic Tumour Screening & Treatment Centre, Imperial College NHS Trust, Charing Cross Hospital.
Matthew C WinterSheffield Centre for Trophoblastic Disease, Weston Park Cancer Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield.
Snezana SusnjarDepartment for Medical Oncology, Institute for Oncology and Radiology Belgrade.
Vesna KesićDepartment of Human Reproduction, Medical Faculty, University of Belgrade, Belgrade, Serbia.
Pierre DescarguesHospices Civils de Lyon, Centre Hospitalier Lyon-Sud, Service de Chirurgie Gynécologique, Pierre Bénite.
Mojgan Devouassoux-ShisheboranHospices Civils de Lyon, Centre Hospitalier Lyon-Sud, Service de Pathologie Multi-Site, Pierre Bénite.
Fabienne AlliasHospices Civils de Lyon, Centre Hospitalier Lyon-Sud, Service de Pathologie Multi-Site, Pierre Bénite.
Baljeet KaurDepartment of Pathology, North West London Pathology, Imperial College NHS Trust.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Uterine placental site trophoblastic tumors (PSTTs) are rare trophoblastic neoplasms, presumed to be of gestational origin. Herein, using a comprehensive morphologic, immunohistochemical, and molecular approach, we describe 5 cases of primary uterine nongestational PSTTs. The median age at presentation was 32 years (range 25 to 45). All tumors were initially expected to be of gestational origin as all were located in the uterus and all patients had a history of pregnancy (5/5, 100%). The median size of the primary uterine tumors was 6.3 cm (range 4.8 to 7.5). Three patients (3/5, 60%) had metastatic disease at presentation or revealed during initial workup (1/5 [20%] patients with lymph node metastasis only and 2/5 [40%] with distant metastases). All tumors showed similar histopathologic and immunohistochemical features to those of gestational PSTTs. The tumor cells expressed hPL in 5/5 (100%) tumors, hCG in 5/5 (100%; focal in all tumors), and GATA3 in 5/5 (100%). However, short tandem repeat (STR) genotyping did not identify any nonpatient alleles in the tumors, indicating a nongestational origin. The median progression-free survival was 18 months (range: 0 to 85) and 2/5 (40%) patients died from disease, highlighting the potential poor prognosis of this nongestational tumor. Thus, in the same way as gestational and nongestational choriocarcinomas are recognized as different entities, nongestational PSTTs could be viewed as a distinct entity from their gestational counterparts, although further investigation and more cases are needed. Furthermore, we propose recommendations for diagnosing and staging of nongestational PSTTs to improve patient stratification and management.

Indexed as

Trophoblastic Tumor, Placental SiteUterine NeoplasmsAdultBiomarkers, TumorFemaleHumansImmunohistochemistryMiddle AgedPregnancyTreatment OutcomeBiomarkers, Tumornongestational trophoblastic tumorPSTTSTR genotypingtrophoblastic differentiationuterine neoplasm

Identifiers

PMID41491402
PMCPMC12978710

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.