Chondromyxoid Fibroma of Phalanges.

Q3 Medicine
Sultan Qaboos University Medical Journal Pub Date : 2025-05-02 eCollection Date: 2025-01-01 DOI:10.18295/squmj.10.2024.068
Lubna S Khan, Sifa Farheen, Vijay K Pandey, Vinay P Singh, Manoj G Madakshira
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引用次数: 0

Abstract

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.

指骨软骨粘液样纤维瘤。
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结合。它可以影响任何年龄的任何骨骼,没有性别偏好。我们报告了一例47岁的女性CMF患者,她于2024年在印度加尔各答的一家三级保健医院出现左小指肿胀。影像学显示一分叶状病变,起源于左小指中指骨,延伸至远指骨基部。细针吸细胞学显示中度细胞黏液样病变。组织病理学检查仍然是诊断的关键,显示一个分叶状肿瘤,具有梭形到星状细胞区,与细胞间隙丰富的粘液样和软骨样基质相关。治疗包括完全切除无肿瘤边缘,因为局部刮除可能发生复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
0.00%
发文量
86
审稿时长
7 weeks
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