Başarir Kerem, Saglik Yener, Yildiz Yusuf
Orthopedics and Traumatology Department, Faculty of Medicine, Ankara University, Samanpazari, Ankara, Turkey.
Hand Surg. 2008;13(2):99-102. doi: 10.1142/S0218810408003876.
Benign fibrous histiocytoma (BFH) of the bone is a rare benign lesion characterised by the presence of fibroblasts and histiocytes. Fibrohistocytic lesions involving bone with identical histological appearances are common during childhood such as fibrous cortical defect. However, BFH is very rare and can only be differentially diagnosed with its presentation, localisation and radiologic features. Here we describe a 33-year-old man with BFH in a rare location, a phalanx. To our knowledge this is the second reported case of a BFH involving the proximal phalanx of the thumb in an adult. We report clinical, radiologic and histological findings of the case and briefly review the literature on the subject.
骨良性纤维组织细胞瘤(BFH)是一种罕见的良性病变,其特征是存在成纤维细胞和组织细胞。儿童时期常见累及骨骼且组织学表现相同的纤维组织细胞性病变,如纤维皮质缺损。然而,BFH非常罕见,只能通过其临床表现、定位和放射学特征进行鉴别诊断。在此,我们描述一名33岁男性,其BFH发生于罕见部位——指骨。据我们所知,这是第二例报道的成人拇指近节指骨发生BFH的病例。我们报告该病例的临床、放射学和组织学表现,并简要回顾关于该主题的文献。