ArticleCureus2026
Extra-abdominal Desmoid Tumor in a 23-Year-Old Male: A Case Report.
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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0 citing papers in PubMed.
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Desmoid tumors are rare, locally aggressive neoplasms that can develop in various anatomical locations. Accurate diagnosis requires a high level of suspicion, as these tumors can resemble other soft tissue sarcomas. This case report discusses a 23-year-old male with a symptomatic thigh mass, highlighting the importance of biopsy and immunohistochemical staining to distinguish desmoid tumors from malignant tumors. We also examine genetic predispositions, evolving management strategies, and the potential of novel therapies such as nirogacestat. Due to the high recurrence rate and unpredictable nature of desmoid tumors, long-term monitoring and a multidisciplinary approach are essential for achieving optimal patient outcomes.
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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 OpenQuestion graph.