Sellar/Juxtasellar Calcification
Anne G. Osborn, MD, FACR
DIFFERENTIAL DIAGNOSIS
Common
Physiologic Calcification, Vascular
Physiologic Calcification, Dura
Atherosclerosis, Intracranial
Saccular Aneurysm
Meningioma
Craniopharyngioma
Neurocysticercosis
Less Common
Astrocytoma
Pilocytic Astrocytoma
Diffuse Astrocytoma, Low Grade
Pilomyxoid Astrocytoma
Chordoid Glioma
Dermoid Cyst
Arteriovenous Malformation
Rare but Important
Cavernous Malformation
Chordoma, Clivus
Pituitary Macroadenoma
Chondrosarcoma, Skull Base
Rathke Cleft Cyst
Benign Nonmeningothelial Tumors
Chondroma
Osteochondroma
Osteoma
ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
Is patient asymptomatic?
Is calcification physiologic or pathologic?
Physiologic
Vascular (age-related changes of ASVD)
Dural (petroclinoid ligament often calcified)
Pathologic
Look for associated mass in/around sella, cavernous sinus
Anatomic sublocation important
Dura (cavernous sinus, tentorium, petroclinoid ligaments) calcifies but less often than falx
Arteries (cavernous/supraclinoid ICA) physiologic Ca++ common
Pituitary, infundibulum, hypothalamus almost never show physiologic Ca++
Helpful Clues for Common Diagnoses
Physiologic Calcification, Vascular
Juxtasellar dura, vessels, not brain
Atherosclerosis, Intracranial
Some age-related ASVD Ca++ normal, physiologic
Relationship to stenosis, stroke controversial
Thickness of Ca++ plaque does not correlate directly with luminal stenosis
Dense, globular Ca++ may be more significant than mural/laminar
Some authors suggest high grade of cavernous ICA Ca++ correlates with small (not large) vessel ischemia
Saccular Aneurysm
Supra/juxtasellar > intracavernous
Mural Ca++ common
Can be rim, globular
Aneurysm often partial/completely thrombosed
Meningioma
Ca++ 20-25%
Diffuse or focal
Solid (“brain rock”) or scattered
Ca++ pattern highly variable
Psammomatous (“sand-like”) or “sunburst” > globular > rim
Look for dural “tail”
Look for changes in adjacent planum sphenoidale
Can cause blistering, hyperostosis, hypertrophied ethmoid or sphenoid sinuses (“pneumosinus dilatans”)
Craniopharyngioma
In children, 90% cystic, 90% Ca++ (rim, globular)
Adults often solid with globular Ca++
Neurocysticercosis
Healed racemose NCC in basal cisterns may Ca++
Helpful Clues for Less Common Diagnoses
Astrocytoma
Pilocytic Astrocytoma
Common in optic chiasm/hypothalamus/3rd ventricle (2nd most common location after cerebellum)
Enhancement varies (none to striking)
Ca++ uncommon in supratentorial PAs!
Diffuse Astrocytoma, Low Grade
WHO grade II may calcify but uncommon in this location
No enhancement
Pilomyxoid Astrocytoma
Rare tumor; common location
Hemorrhage common, Ca++ uncommon
Chordoid Glioma
Newly described distinct tumor entity
Hypothalamus/anterior 3rd ventricle mass
Ovoid, well-circumscribed
Usually solid mass; may have associated cysts (rare)
Hyperdense on NECT
Ca++ uncommon
Hypointense on T1-, iso- to mildly hyperintense on T2WI
Enhances strongly, usually uniformly
Dermoid Cyst
Sellar/parasellar/frontonasal region most common site
Unilocular fat-like cyst
Look for “droplets” in sulci, cisterns (ruptured dermoid)
20% have capsular Ca++
Arteriovenous Malformation
Supra/juxtasellar < hemispheres
25-30% Ca++
Helpful Clues for Rare Diagnoses
Cavernous Malformation
Common lesion that commonly shows Ca++
Hypothalamus, juxtasellar lesions uncommon
Chordoma, Clivus
35% arise in skull base
Epicenter at sphenooccipital synchondrosis
Destructive, invasive
Often have “thumb-like” posterior tumor extension through clivus
50% contain ossific fragments of destroyed bone on NECT
Hyperintense on T2WI
Pituitary Macroadenoma
Most common lesion in this location
Only 1-2% Ca++
Can be very invasive, destructive
Chondrosarcoma, Skull Base
Epicenter at petro-occipital fissure
50% have chondroid calcification in tumor matrix (arcs, rings)
Hyperintense on T2WI
Enhance strongly, heterogeneously
Whorls of enhancing lines within tumor matrix
Rathke Cleft Cyst
Only 10-15% Ca++ vs. > 90% of craniopharyngioma
Calcified RCC may be indistinguishable
Benign Nonmeningothelial Tumors
Chondroma, osteochondroma, osteoma may all show Ca++ in cap or tumor matrix
Rare cause of juxtasellar Ca++Stay updated, free articles. Join our Telegram channel
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