Basal Ganglia Calcification
Karen L. Salzman, MD
DIFFERENTIAL DIAGNOSIS
Common
Aging Brain, Normal
Neurocysticercosis
Less Common
Fahr Disease
Hypoxic-Ischemic Injury, NOS
MELAS
Congenital Infections
HIV, Congenital
CMV, Congenital
Endocrinologic Disorders
Hyperparathyroidism
Hypoparathyroidism
Pseudohypoparathyroidism
Pseudopseudohypoparathyroidism
Hypothyroidism
Toxoplasmosis, Acquired
Leigh Syndrome
Tuberculosis
Radiation and Chemotherapy
Cavernous Malformation (Mimic)
Vascular Calcification (Mimic)
Tuberous Sclerosis Complex (Mimic)
Rare but Important
Hallervorden-Spatz Syndrome
CO Poisoning
Parasites, Miscellaneous
ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
Basal ganglia (BG) Ca++ is end result of multiple toxic, metabolic, inflammatory, and infectious insults
Location of Ca++ helpful to determine underlying cause (globus pallidus [GP] vs. putamen vs. caudate)
Patient age may impact differential diagnosis
Helpful Clues for Common Diagnoses
Aging Brain, Normal
Commonly affects GP more than putamen
Seen in aging brain as normal variant
Typically in patients older than 30 years
If occurs with other Ca++, consider pathologic condition
Neurocysticercosis
May occur anywhere in brain
Convexity subarachnoid spaces most common
Imaging varies with pathologic stage
Ca++ in nodular calcified (healed) stage
Helpful Clues for Less Common Diagnoses
Fahr Disease
Bilateral symmetric BG Ca++, often with Ca++ in other locations
GP is most common site of Ca++ (lateral > medial)
Other locations: Putamen, caudate, thalami, dentate nuclei of cerebellum, cerebral white matter, internal capsule
Associated abnormalities: Parkinsonism in autosomal dominant FD
Hypoxic-Ischemic Injury, NOS
HIE, term: Profound acute injury results in decreased BG and thalamic density, ± hemorrhage acutely
Lateral thalami and posterior putamen typical
May show Ca++ in chronic phase
HIE in adults: Putamen > GP typically
May have history of “anoxic event”
MR > CT for acute changes
May show Ca++ in chronic phase
MELAS
BG Ca++ in child or young adult with cortical lesions (parietooccipital > temporoparietal)
HIV, Congenital
Symmetric BG Ca++ and cerebral atrophy
GP and putamen > caudate
Subcortical WM Ca++ common
Ca++ occur in a fairly symmetric fashion a result of a calcific vasculopathy of medium and small arteries
CMV, Congenital
Periventricular Ca++, microcephaly, and cortical dysplasia characteristic
Periventricular > > BG Ca++
Endocrinologic Disorders
Bilateral BG: GP and putamen, dentate nuclei, thalami, subcortical areas
Ca++ in primary hypoparathyroidism is more diffuse than in other etiologies of Ca++
Toxoplasmosis, Acquired
Typically multifocal, but BG common site (up to 75%)
Enhancing lesion most common acutely
Post-therapy, Ca++ is common
Leigh Syndrome
Bilateral, symmetric ↑ T2/FLAIR putamina and peri-aqueductal gray matterStay updated, free articles. Join our Telegram channel
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