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Lymphocytic hypophysitis (LH)
Synonyms: Adenohypophysitis, primary hypophysitis, stalkitis
Idiopathic inflammation of pituitary gland &/or stalk
Thick stalk (> 2 mm + loss of normal “top to bottom” tapering)
± enlarged pituitary gland
75% show loss of posterior pituitary “bright spot”
Enhances intensely, uniformly
May have adjacent dural or sphenoid sinus mucosal thickening
Macroadenoma
Pituitary hyperplasia
Adolescent pituitary gland
Granulomatous disease
Pituitary “dwarf”
Ectopic posterior pituitary gland
Peripartum woman with headache, multiple endocrine deficiencies
Middle-aged man with diabetes insipidus (lymphocytic infundibuloneurohypophysitis)
Mean in women = 35 years, men = 45 years
M:F = 1:8-9
Often self-limited
Unrecognized, untreated LH can result in death from panhypopituitarism
Conservative care (steroids, hormone replacement)
LH can mimic pituitary adenoma
.
. Surgery for optic chiasm decompression disclosed lymphocytic hypophysitis. Imaging mimics pituitary macroadenoma.
in a 37-year-old man with panhypopituitarism during treatment with ipilimumab for metastatic melanoma. The gland had doubled in size since MR 6 weeks prior. Findings are consistent with drug-induced hypophysitis.
related to lymphocytic infundibuloneurohypophysitis.
Lymphocytic hypophysitis (LH)
Adenohypophysitis, primary hypophysitis, stalkitis
Idiopathic inflammation of pituitary gland or stalk
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