ArticleCureus2026
Paratesticular Solitary Fibrous Tumor: A Case Report With Sonographic and Histopathologic Insights.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
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0 citing papers in PubMed.
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Solitary fibrous tumor (SFT) is a rare mesenchymal neoplasm of fibroblastic differentiation that is generally considered benign. It most commonly arises from the pleura, typically presenting as a thoracic mass. Extrapleural occurrence, particularly within the urogenital tract, such as the paratesticular region, is exceedingly rare. The histopathological characteristics of paratesticular SFTs are similar to those observed in tumors arising at other anatomical sites. We report the case of a 26-year-old man presenting with a painless, firm, and mobile paratesticular mass that had progressively enlarged over two years. The lesion was completely excised surgically without perioperative complications. Gross and histopathological examination demonstrated a well-circumscribed lesion composed of uniform spindle cells embedded in a dense collagenous stroma. Immunohistochemical analysis showed diffuse positivity for cluster of differentiation 34 (CD34). These findings supported the diagnosis of paratesticular SFT.
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