We encountered a 91-year-old patient with acromegalic features. The se
rum levels of growth hormone (GH) and insulin-like growth factor-I (IG
F-I) were increased to 23.3 ng/ml and to 268 ng/ml, respectively. Both
thyrotropin-releasing hormone and luteinizing hormone-releasing hormo
ne tests demonstrated a 2-3 fold increase in the serum GH level. Magne
tic resonance imaging disclosed a pituitary mass in the enlarged sella
. The patient was diagnosed as having acromegaly due to overproduction
of GH from a pituitary tumor. She manifested cardiac hypertrophy with
severe aortic stenosis and mild hypertension, but without diabetes me
llitus. After the administration of octreotide subcutaneously at a dos
e of 25 to 50 mu g daily for 20 days, the serum GH level increased tra
nsiently but decreased rapidly to approximately half the initial level
, and suppression of the GH level persisted thereafter for over 2.5 mo
nths. This patient seems to be the oldest patient with acromegaly amon
g those reported in Japan.