Why the study?
Primary atypical fibrous histiocytoma of the temporal bone is exceptionally rare and can mimic other destructive skull lesions on imaging and intraoperative inspection.
Primary AFH of the temporal bone is a rare tumor requiring careful histopathologic diagnosis and complete surgical excision with long-term follow-up.
AFH should be considered in temporal bone tumors with appropriate IHC workup; extends known primary sites and leaves open recurrence risk after excision.
Primary AFH of the temporal bone is an exceptionally rare entity that can mimic other destructive skull lesions on imaging and intraoperative inspection. Accurate diagnosis relies on careful histopathologic evaluation and exclusion of histologic mimickers using a comprehensive immunohistochemical panel. Complete surgical excision remains the cornerstone of treatment, and long-term follow-up is recommended due to the tumor's intermediate malignant potential.
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Dong et al. (2026) studied this question.
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