Clival and Paraclival Lesions: Imaging Features and Differential Diagnosis
A practical radiology review of Clival and Paraclival Lesions: Imaging Features and Differential Diagnosis, focused on imaging findings, differential diagnosis, reporting...

A practical radiology review of Clival and Paraclival Lesions: Imaging Features and Differential Diagnosis, focused on imaging findings, differential diagnosis, reporting points, and high-yield teaching pearls.
Anatomy & Physiology Pearls
- Spheno-occipital synchondrosis → fuses late teens–mid-20s ⏳ → incomplete fusion in young = don’t confuse with lytic lesion
Normal clival marrow
- T1 ≥ pons = normal
- T1 < pons = suspect pathology (marrow replacement, edema, tumor)
Marrow grading
- Grade 1: >50% low T1 signal
- Grade 2: 20–50%
- Grade 3: <20% (fatty)
- Useful for early infiltration detection in myeloma/metastases
Sequences
- FIESTA/CISS = tiny lesion detector
- Great for Ecchordosis physaliphora (EP) or small cystic lesions near brainstem
- Can show communication with prepontine cistern → diagnostic for EP
DWI/ADC
- Chordoma: ADC ↓ (restricted)
- Chondrosarcoma: ADC ↑ (more free diffusion)
- Skull Base Ostemyelitis: ADC ↑↑ (infection/inflammation = not restricted )
- NPC/Lymphoma: ADC ↓ (cellularity)
- ADC = secret diagnostic weapon for skull base differentiation
Benign Lesions
- Fibrous dysplasia
- Ground-glass CT texture = pathognomonic
- T1 ↓, T2 variable (depending on fibrous vs cystic)
- Can mimic meningioma hyperostosis — meningioma enhances dural-based; FD is intramedullary
- Only 44 clival cases ever reported → extreme rarity clue
- Benign-appearing notochordal lesion (BNL)
- Ecchordosis physaliphora (EP) ≠ Chordoma
- EP: non-enhancing, CSF-like signal, often on posterior clival surface, stalk-like attachment to dura
- Chordoma: enhancing, expansile, bone destruction
- Stable over time → 6-month MRI follow-up recommended
Malignant Lesions— Subtle Differentiation
Chordoma
- Classic “honeycomb” enhancement pattern
- May show hemorrhagic foci → T1 bright spots
- High recurrence even if low grade
- Pitfall: low-T2 chordoma = mimic metastasis or lymphoma
Chondrosarcoma
- Off-midline (petro-occipital synchondrosis)
- Popcorn / ring-and-arc calcification = chondroid matrix clue
- ADC higher than chordoma
- Tends to remodel bone (vs destructive)
Myeloma
- 5 marrow patterns: normal / focal / diffuse / salt-pepper / mixed
- “Normal marrow” pattern can still mean active disease — rely on clinical + lab correlation
Metastasis
- Mixed lytic–sclerotic (esp. breast, prostate )
- Multifocality + different lesion stages = metastatic clue
- ADC ↓ in high-cellular types; ↑ in necrotic ones
Infectious / Inflammatory — Diagnostic Traps
- Central Skull Base Osteomyelitis (SBO)
- Often starts as sinus infection → spreads to clivus
- MRI: T1 ↓, T2 variable, contrast ↑ diffuse
- ADC ↑ (helps distinguish from tumor)
- Common bug: Pseudomonas (esp. diabetics)
- Bone changes lag clinical response → follow-up based on CRP/ESR, not imaging
- FDG-PET may stay positive even after MRI normalization — persistent metabolic activity ≠ relapse
Secondary / Adjacent Spread Lesions
NPC
- Iso–hyper T2, diffusion restriction, strong enhancement
- Clival involvement = T3 disease per AJCC
- Often shows perineural spread → follow CN V2–V3 course
- Sinonasal malignancy
- Mucinous → T2 bright
- Non-mucinous → T2 dark
- Enhancement pattern > signal intensity for tumor typing
- Lymphoma vs carcinoma → Lymphoma enhances homogeneously, shows restricted diffusion, no necrosis
PitNET (macroadenoma)
- Now officially malignant (“3” code in WHO 5th ed)
- Extrasellar ones can arise from clivus = ectopic PitNET
- Hypointense/isointense T1, variable T2, mild enhancement
Intraosseous meningioma
- Osteoblastic type = hyperostosis
- Osteolytic type = can mimic metastasis
- Homogeneous enhancement helps ID
Clinical use note
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