BACKGROUND: Acromegaly is frequently associated with degenerative join
t disease, but only a few cases of typical seronegative polyarthritis
related to excessive growth hormone secretion have been reported. CASE
REPORT: A 76-year-old man had edematous polyarthritis with an atypica
l course over the last 5 years. Acromegaly had gone undetected and the
discovery of an adenoma of the anterior pituitary led to the prescrip
tion of somatostatin. Remission of the polyarthritis syndrome followed
treatment DISCUSSION: RS3PE (remitting, seronegative, symmetrical, sy
novitis with pitting edema) rheumatoid disease could be discussed in t
his case where joint disease developed slowly due to low level growth
hormone oversecretion. Acromegaly should be entertained as a possible
diagnosis in patients with atypical inflammatory polyarthritis resista
nt to antiinflammatory therapy. (C) 1998, Masson, Paris.