Table 5.
Summary of the paraspinal tumours-like lesions discussed in this article with their clinical and imaging features
Tumour mimics | Notable clinical signs | US (For superficial masses) | Notable CT pattern | Notable MRI pattern |
---|---|---|---|---|
Traumatic disorders | History of trauma |
Haematoma: Compressible fluid collection Low echogenicity Septa Fat necrosis: Compressible fluid collection Morel lavallée: Compressible fluid collection |
Haematoma: Hyperdensity |
Haematoma: Signal changes on T1 and T2 with evolving breakdown products Low signal on T2WI Blooming artefact of T2WI Fat necrosis: Fibrous tissue (low signal) intermixed with adipose tissue (high signal) Peripheral enhancement Morel lavallée: Fluid collection |
Degenerative disorders |
> 50 y Spinal degenerative disorders Lumbar predominance |
– |
Degenerative features: Vertebral narrowing, facet hypertrophy, sclerosis, osteophyte |
Bursitis: fluid-like signal Cystic formation Fibrous nodules: Low signal on all sequences |
Infection | Increase with age | – |
Erosive facet joint Erosive vertebral endplate |
Inflammation: Imaging psoas sign Abscess: Rim enhancement Central attenuation |
HEM |
Myeloproliferative neoplasm Chronic haematological disorders |
– |
Multifocal—bilateral Skeletal changes related with chronic anaemia |
Smoothy loculated Homogeneous signal Fatty replacement and iron deposition in older masses |
MOC |
History of trauma Repeated minor injuries Rapidly growing painful |
– | Peripheral zonal ossification | Change with time |
y, years; WI, weighted imaging