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A rare self-limiting, rapidly growing, non-encapsulated benign neoplasm that arises from the cranium. This is an osteolytic lesion. It is characterized by the presence of plump spindle-shaped fibroblasts, multinucleated osteoclast-like giant cells, chronic inflammatory infiltrate, red blood cell extravasation, and high mitotic activity.
No clinical trials have been registered for cranial nodular fasciitis.
5 publications have been identified in PubMed for cranial nodular fasciitis. Research spans Case Report / Case Series (60%) and Review / Meta-Analysis (40%).
Qiao YD (2026). [PMID: 41490638](https://pubmed.ncbi.nlm.nih.gov/41490638/). *Zhonghua bing li xue za zhi = Chinese journal of pathology*. [Case Report / Case Series]
González-Fuentes JM (2025). [PMID: 40136575](https://pubmed.ncbi.nlm.nih.gov/40136575/). *Clinics and practice*. [Case Report / Case Series]
Syed S (2025). [PMID: 40348771](https://pubmed.ncbi.nlm.nih.gov/40348771/). *Cell death discovery*. [Review / Meta-Analysis]
Bhola N (2025). [PMID: 40361180](https://pubmed.ncbi.nlm.nih.gov/40361180/). *Journal of medical case reports*. [Case Report / Case Series]
Atak F (2025). [PMID: 40751802](https://pubmed.ncbi.nlm.nih.gov/40751802/). *Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery*. [Review / Meta-Analysis]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 11:55 AM UTC