Nj. Sarlis et al., MRI-DEMONSTRABLE REGRESSION OF A PITUITARY MASS IN A CASE OF PRIMARY HYPOTHYROIDISM AFTER A WEEK OF ACUTE THYROID-HORMONE THERAPY, The Journal of clinical endocrinology and metabolism, 82(3), 1997, pp. 808-811
Although magnetic resonance imaging (MRI) characteristics of pituitary
gland hyperplasia in primary hypothyroidism have been previously desc
ribed, the time span necessary for the regression of the hyperplasia i
n response to acute thyroid hormone (TK) therapy has not been defined.
A 26-yr-old woman underwent I-131 ablation 11 yr before admission. In
termittent poor compliance to levothyroxine (LT4) therapy led to inapp
ropriately high serum thyroid-stimulating hormone (TSH) for her triiod
othyronine (T3) and thyroxine (T4) levels. The patient was investigate
d to rule out TSH-secreting pituitary adenoma or resistance to TH. On
admission, the patient's clinical features and thyroid function tests,
as well. as thyrotropin-releasing hormone (TRH) and acute T3 suppress
ion tests, were in favor of profound primary hypothyroidism. MRI revea
led symmetrical enlargement of the pituitary gland with distinct morph
ological characteristics of a macroadenoma. The patient began high-dos
e TH therapy and was rescannned six days later. The follow-up scan rev
ealed a dramatic shrinkage of the pituitary gland. Four weeks later, s
erum T4 and TSH were within the normal range, and repeat MRI scan of t
he pituitary at that time showed a normal gland. This case is the firs
t to document dramatic shrinkage of pituitary hyperplasia in long-stan
ding primary hypothyroidism within one week of acute TH therapy. MRI a
lone is unable to reliably differentiate between a TSH-secreting pitui
tary adenoma and hypothyroidism-induced pituitary hyperplasia. Dynamic
endocrine testing as well as repeat pituitary MRI after a brief TH tr
ial may provide a firm diagnosis in similar cases.