Khan Lubna S, Farheen Sifa, Pandey Vijay K, Singh Vinay P, Madakshira Manoj G
Departments of Pathology, Command Hospital, Kolkata, India.
Department of Pathology, Base Hospital, Barrackpore, India.
Sultan Qaboos Univ Med J. 2025 May 2;25(1):168-174. doi: 10.18295/squmj.10.2024.068. eCollection 2025.
Chondromyxoid fibroma (CMF) is a rare, benign metaphyseal bone tumour characterised by a combination of chondroid, myxoid, and fibrous elements. It can affect any bone at any age, with no gender predilection. We report a case of CMF in a 47-year-old female patient who presented with swelling of the left little finger at a tertiary care hospital in Kolkata, India, in 2024. Imaging revealed a lobulated lesion originating from the middle phalanx of the left little finger, extending to involve the base of the distal phalanx. Fine needle aspiration cytology indicated a moderately cellular myxoid lesion. Histopathology, which remains crucial for diagnosis, showed a lobulated tumour with zones of spindle to stellate cells, associated with an abundant myxoid and chondroid matrix in the intercellular spaces. Treatment involves complete local excision with tumour-free margins, as recurrence may occur with local curettage.
软骨黏液样纤维瘤(CMF)是一种罕见的良性干骺端骨肿瘤,其特征是软骨样、黏液样和纤维成分的组合。它可在任何年龄影响任何骨骼,无性别倾向。我们报告一例CMF病例,患者为一名47岁女性,2024年在印度加尔各答的一家三级护理医院因左手小指肿胀就诊。影像学检查显示一个分叶状病变起源于左手小指中节指骨,延伸至远节指骨基部。细针穿刺细胞学检查提示为中度细胞性黏液样病变。对诊断至关重要的组织病理学检查显示为分叶状肿瘤,有梭形至星状细胞区域,细胞间隙有丰富的黏液样和软骨样基质。治疗方法是进行切缘无肿瘤的完整局部切除,因为局部刮除可能会复发。