In order to define the clinical associations and diagnostic meaning of
anticentromere antibodies in a random population of patients, clinica
l and serological findings were studied with the evolution of 16 patie
nts selected only because of their positiveness to anticentromere anti
bodies, detected by indirect immunofluorescence on HEp-2 cells and con
firmed in chromosome spreads of HMcB cells. The most frequent diagnosi
s was systemic sclerosis in 9 patients (56%) especially in its variety
Limited Cutaneous Systemic Sclerosis /CREST (7 patients). The rest of
the cases (44%) showed different diseases (3 isolated Raynaud's pheno
mena, 1 Sjogren's syndrome, 1 seronegative polyarthritis, 1 undifferen
tiated connective tissue disease and a probable sarcoidosis). Therefor
e, even tough the more frequent clinical entity associated to anticent
romere antibodies was systemic sclerosis and especially its variety Li
mited Cutaneous Systemic Sclerosis /CREST its diagnostic specificity i
s relatively low. The most frequent clinical association in our group
of patients with positive anticentromere antibodies has been Raynaud's
phenomena, alone or associated to other processes, being found in all
but one of the studied patients (94%).