Case report highlights rapid axSpA progression with early imaging features in a 55-year-old man.
Axial spondyloarthritis (axSpA) is a chronic inflammatory disease that primarily affects the sacroiliac joints and spine, leading to progressive structural changes. The clinical course of axSpA is heterogeneous, and cases of rapid structural progression over a relatively short period have been reported. With the advent of biologic agents, it is now possible to suppress structural damage, highlighting the importance of early diagnosis and treatment. However, reports describing the early features of rapidly progressive axSpA are limited. We report the case of a 55-year-old man who presented with low back pain following a fall. Imaging revealed a vertebral fracture at T12/L1 and a bamboo spine, and he underwent percutaneous posterior fixation. Sacroiliac joint ankylosis was also observed, and a diagnosis of ankylosing spondylitis (AS) was made. The patient had visited our hospital nine years earlier for low back pain. At that time, MRI showed diffuse bone marrow edema (BME) across multiple vertebrae and depression of the vertebral endplates. However, the edema was not localized to vertebral corners, and the findings were interpreted as Schmorl’s nodes with surrounding edema. Based on the current findings, the previous imaging was retrospectively interpreted as an early sign of axSpA. This case highlights that diffuse vertebral BME without typical corner lesions may signal rapidly progressive axSpA. Recognition of such atypical early imaging features is critical to ensure timely diagnosis and management.
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Kai et al. (2026) studied this question.
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