ArticleCureus2026
Myoid Gonadal Stromal Tumor of the Testis: A Rare Sex Cord-Stromal Neoplasm in a Young Man.
Article in Cureus, 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
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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.
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Myoid gonadal stromal tumor is a rare subtype of testicular sex cord-stromal tumor characterized by a mixture of myoid and gonadal spindle cells. We present a 24-year-old man with a two-year history of chronic, intermittent dull pain in the left testicle. Work-up, management, pathology, and follow-up are reviewed. These tumors have demonstrated indolent behavior, typically benign; however, accurate diagnosis is essential to differentiate them from other more dangerous tumor types. Radical orchiectomy alone appears to be sufficient for the treatment of these tumors, with only short-term surveillance appearing adequate due to their indolent nature.
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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 Socratic graph.