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IgG4-related disease (IgG4-RD)
Chronic fibroinflammatory disease characterized by IgG4(+) plasma cell infiltrates
Diffusely infiltrating enhancing mass
Orbital adnexa (lacrimal gland most common)
Dura-arachnoid (IgG4-related hypertrophic pachymeningitis)
Pituitary gland, stalk (hypophysitis)
Other: Cranial nerves (especially infraorbital nerve), brain (autoimmune-like encephalopathy)
MR
Isointense to brain on T1WI, hypointense on T2WI
Enhances strongly, uniformly
Idiopathic inflammatory pseudotumor
Meningioma
Neurosarcoid
Lymphoma
All ages, but 6th-7th decades most common
Exophthalmos, headache
Cranial neuropathy
Clinical course
Glucocorticosteroids → improvement/remission (relapses common if tapered/discontinued)
Between 3-30% of IgG4-RD patients have normal serum IgG4 concentrations
Elevated serum IgG4 is not diagnostic of IgG4-RD (neither sensitive nor specific)
Best diagnostic clue is combination of clinical history, physical examination, laboratory, imaging
IgG4-related disease (IgG4-RD)
Organ-specific conditions now related to IgG4
Mikulicz disease (lacrimal, parotid, submandibular glands)
Autoimmune pancreatitis (AIP)
Ormond disease (retroperitoneal fibrosis)
IgG4-related ophthalmic disease
“Idiopathic” pseudotumor (generic)
Chronic fibroinflammatory disease characterized by IgG4(+) plasma cell infiltrates
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