Arif Hamza, Faheem Muhammad Shaheer Bin, Memon Munawer Latif, Shaheryar Khawaja, Monawwer Syed Abdullah, Samadi Sumaya
Department of Surgery POF Hospital Wah Cantt Pakistan.
Department of Medicine and Surgery Karachi Institute of Medical Sciences, KIMS Karachi Pakistan.
Clin Case Rep. 2025 Jul 6;13(7):e70600. doi: 10.1002/ccr3.70600. eCollection 2025 Jul.
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.
细胞性血管纤维瘤（CAF）是一种罕见的良性肿瘤，预后良好。由于其非特异性的临床和影像学特征，CAF的诊断可能具有挑战性，这常常导致误诊，就像我们这位77岁男性患者的病例一样。组织病理学和免疫组织化学在识别CAF并将其与恶性肿瘤区分开来方面起着关键作用。尽管报道的复发病例不多，但仍应考虑进行长期随访。
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