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Peer-reviewed veterinary case report

Computed tomography identifies the proximodorsomedial subchondral bone of equine central tarsal bones as a predilection site for sclerosis, demineralisation and associated fractures.

Journal:
Equine veterinary journal
Year:
2026
Authors:
Campana, Sandra et al.
Affiliation:
Clinic for Diagnostic Imaging
Species:
horse

Abstract

BACKGROUND: The distribution pattern of central tarsal bone (CTB) changes has not been described, except for slab- and dorsomedial-plantarolateral fractures. OBJECTIVES: To describe CTB changes in CT and document their distribution and associations. STUDY DESIGN: Retrospective case series. METHODS: Standing and recumbent tarsal CT studies from 94 clinical cases were retrospectively evaluated. General case information, degree of sclerosis (none-severe), lesions (demineralisation, cystoid, fissure/fracture) and their location were recorded, dividing CTBs into 8 regions. RESULTS: Eighty five of 94 tarsi showed at least one region of moderate to severe sclerosis, of which 90% affected the dorsomedial region. The prevalence of lesions was significantly associated with higher degrees of sclerosis (p = 0.04) at this site. Of 32 demineralising lesions, 21 were in the proximal subchondral bone dorsomedially. Twenty-four CTBs showed fissures/fractures; 19/24 were in a dorsomedial-plantarolateral direction, and 17/19 were associated with demineralisation. Of five fissures/fractures with different configurations, none had associated demineralisation. There were 27 cyst-like lesions, 21/27 in the distal subchondral bone, of which almost half (13/27) located medially. MAIN LIMITATIONS: Retrospective design; heterogeneous, warmblood-oriented population; no clinical correlation of findings nor histological confirmation of described changes. CONCLUSIONS: Given the links between sclerosis, demineralisation and fissures/fractures, the dorsomedial proximal subchondral bone plate of the CTB must be scrutinised both in CT and radiography.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/40703020/