ArticleCureus2026
Sinonasal Phosphaturic Mesenchymal Tumor Presenting With Tumor-Induced Osteomalacia: A Rare Case and Review of the Literature.
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
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Phosphaturic mesenchymal tumor (PMT) is a rare tumor involving bone and soft tissues, usually benign and solitary. They mainly affect the extremities and are rarely seen in the head and neck region. They are most commonly associated with tumor-induced osteomalacia (TIO). TIO, also known as oncogenic osteomalacia, is a paraneoplastic syndrome in which tumor cells secrete hormones that reduce mineralization of mature bone, thereby decreasing osteoblastic activity and causing renal phosphate wasting. One of the most common hormones involved is fibroblast growth factor-23 (FGF-23), which belongs to a group of
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