Chondromyxoid Fibroma of Phalanges

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.

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Publication Details

Journal
Sultan Qaboos University medical journal
Published
2024-10-31
DOI
https://doi.org/10.18295/squmj.10.2024.068
Primary Topic
Bone Tumor Diagnosis and Treatments
Type
article
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article

Chondromyxoid Fibroma of Phalanges

Lubna Khan, Vijay Kumar Pandey, Manoj Gopal Madakshira, Vineeta Singh et al.
Sultan Qaboos University medical journal
Bone Tumor Diagnosis and Treatments
article

Chondromyxoid Fibroma of Phalanges

Lubna Khan, Vijay Kumar Pandey, Manoj Gopal Madakshira, Vineeta Singh, Sifa Farheen
article en

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.

Sultan Qaboos University medical journalVol. 25(1)
Command Hospital (IN)
Good health and well-being
Openalex Percentile: Top 66%
Bone Tumor Diagnosis and Treatments
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