Solitary fibrous tumor in the temporalis muscle: a case report and literature review
- PMID: 37919910
- PMCID: PMC10622951
- DOI: 10.7181/acfs.2023.00199
Solitary fibrous tumor in the temporalis muscle: a case report and literature review
Abstract
Solitary fibrous tumor (SFT) is an infrequently occurring neoplasm most commonly observed in the pleura, but it can develop in the head and neck region in occasional cases. However, no reports have described SFT in the temporalis muscle. Herein, we present the first known case of SFT in the temporalis muscle. A 47-year-old man complained of a painless palpable mass on his right temple. Facial enhanced computed tomography identified a 4.0× 2.9× 1.4 cm mass presenting as a vascular tumor in the right temporalis muscle under the zygomatic arch. The mass was excised from the right temporalis muscle under general anesthesia. A histopathologic examination revealed that the mass was an SFT. No complications occurred after surgery, including functional disability or sensory loss. The patient was followed up for 3 months without complications. Although SFT in extrapulmonary regions is rare, it should be considered in the differential diagnosis of masses that occur in the temporal area.
Keywords: Case reports; STAT6 transcription factor; Solitary fibrous tumors; Temporal muscle.
Conflict of interest statement
Jun Ho Choi, Jae Ha Hwang, and Kwang Seog Kim serving as editorial board members of the journal were not involved in the following: selection of the peer reviewer, evaluation of the article, and decision process of acceptance of this article. No other potential conflicts of interest relevant to this article were reported.
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