Abstract
Cellular Angiofibroma (CAF) is a rare and benign neoplasm with a good prognosis. Diagnosis of CAF can be challenging due to its nonspecific clinical and radiological features, which can often lead to a misdiagnosis, as in our case of a 77-year-old male. Histopathology and immunohistochemistry play a crucial role in identifying CAF and differentiating it from malignant tumors. Although not many cases of recurrence have been reported, long-term follow-up should still be considered.