ArticleUrology case reports2026
Myoid gonadal stromal tumor: A rare testicular sex cord stromal neoplasm - a case report and review of the literature.
Article in Urology case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Myoid gonadal stromal tumor (MGST) is an exceptionally rare benign testicular sex cord-stromal neoplasm with limited published experience. We report a 30-year-old man presenting with a painless right testicular mass and normal serum tumor markers. Ultrasonography and magnetic resonance imaging demonstrated a small enhancing intratesticular lesion suspicious for malignancy. Radical inguinal orchiectomy was performed. Histopathological and immunohistochemical evaluation was consistent with MGST, showing spindle-cell proliferation with diffuse smooth muscle actin, S100, and vimentin positivity and focal inhibin expression. No recurrence or metastasis occurred during 12 months of follow-up. This case highlights the diagnostic challenge and rarity of MGST.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.