List To Memorise Flashcards
Solitary collapsed vertebra (vertebra plana)
- Osteoporosis
- Neoplastic: met, MM/plasmacytoma, lymphoma
- Trauma
- Infection (with destruction of adjacent disc spaces, except TB which has preserved disc space)
- Eosinophilic granuloma (common cause in childhood, posterior element usually spared)
- Benign tumour eg: haemangioma, GCT, ABC
- Paget’s disease (neural arch is involved usually)
Multiple collapsed vertebrae
- Osteoporosis
- Neoplastic
- Trauma
- Infection
- Langerhans cell histocytosis (children and adolescent, disc enlarged)
- Scheuermann’ disease
- Sickle cell anaemia & Gaucher disease (H-shaped vertebrae)
- Osteogenesis imperfecta
- Osteomalacia
- Hyperparathyroidism
Enlarged vertebral body
Generalised: gigantism, acromegaly
Local:
1. Paget’s disease (picture frame in mixed phase, ivory vertebra in diffuse sclerotic phase)
2. Benign bone tumour (ABC, hemangioma (vertical trabecular pattern), GCT)
3. Fibrous dysplasia
4. Hydatid
Squaring of 1/> vertebral bodies
- Seronegative spondyloarthropathies
- Paget’s disease
- RA
Scoliosis
(Cobb angle > 10) aka spinal asymmetry if < 10 degree
- Idiopathic: congenital, juvenile, adolescent
- Congenital: vertebral, neurological (Chiari malformation, syringomyelia, tethered cord)
- Others: developmental dysplasia, neuromuscular, tumour related, degenerative, post-traumatic, infection
Erosion/destruction/absence pedicle
- Met
- MM
- Intraspinal tumour (eg: ependymoma, nerve sheath tumour)
- TB, other infection
- Radiotherapy
Solitary dense pedicle
- Osteoblastic metastasis
- Osteoid osteoma
- Bone island
- Unilateral spondylolysis
- Congenitally absent/hypoplastic contralateral posterior elements
- Osteoblastoma
- Other sclerotic bone lesions eg: Paget’s disease, fibrous dysplasia, sarcoidosis, tuberous sclerosis
Block vertebrae
- Klippel-Feil syndrome (C2/3, C5/6)
- Isolated congenital
- Juvenile idiopathic arthritis
- Ankylosing spondylitis
- Infectious spondylodiscitis
- Surgical fusion
- Post-traumatic
Ivory vertebral body
- Met
- Paget’s disease
- Haemangioma
- Low grade infection eg: TB
- Lymphoma
- Sarcoidosis
- SAPHO syndrome (synovitis, acne, pustulosis, hyperostosis, osteitis)
Intervertebral disc calcification
- Degenerative spondylosis
- Post-spinal fusion
- Ankylosing spondylitis
- DISH
- CPPD
- HADD
- Haemochromatosis
- Gout
- Hyperparathyroidism
- Amyloidosis
- Alkaptonuria/ochronosis
- Juvenile chronic arthritides
- Idiopathic
Atlantoaxial subluxation
>3mm adult, >5mm child
- Osseous or ligamentous injury (eg: transverse ligament)
- RA
- Psoriatic arthropathy
- CPPD
- HADD
- SLE
- AS
- Juvenile idiopathic arthritis
- Infection eg: epidural phelgmon/abscess
- Congenital hypoplasia
- Griselda syndrome (laxity of transverse/alar ligament
Bony outgrowth of spine
- Osteophytes
- Syndesmophytes (AS, CPPD, haemachromatosis, onchronosis)
- Non-marginal osteophytes / paravertebral ossification (psoariatic arthropathy, chronic reactive arthropathy, SAPHO)
- Undulating anterior or posterior ossification (DISH - anterior ossificatio, >3 contiguous vertebrae, dish height preserved; ossification of PLL)
Posterior scalloping of vertebral bodies (SALMON) - Mnemonic
S: spinal cord tumour (astrocytoma, ependymoma, schwannoma)
A: achondroplasia, acromegaly
L: Loeys-Dietz syndrome (and other connective tissue disorder)
M: Marfan’s syndrome, mucopolysaccharidoses
O: Osteogenesis imperfecta
N: neurofibromatosis type 1
Posterior scalloping of vertebral bodies
- Spinal cord tumour: ependymoma, dermoid, lipoma, nerve sheath tumour, meningioma
- Neurofibromatosis: due to mesodermal dysplasia and dural ectasia
- Syringomyelia
- Communication hydrocephalus (if severe and untreated)
- Acromegaly
- Achondroplasia
- Other congenital syndromes: Ehlers-Danilo’s/Marfan, osteogenesis imperfecta
Anterior vertebral scalloping
- Aortic aneurysm
- Lymphadenopathy
- Delayed motor development eg: Down syndrome