A case of a patient with an uncommon thyroid carcinoma, showing histologica
l and immunohistochemical features of both follicular and parafollicular ce
lls is described. Somatic point mutation (ATG to ACG heterozygotic mutation
at codon 918) of the RET proto-oncogene was detected in tumor tissue, as c
onfirmed by immunohistochemical expression of RET oncoprotein. Our findings
suggest that constitutive RET proto-oncogene activation may be involved in
the development of mixed medullary-follicular thyroid carcinoma. (C) 2001,
Editrice Kurtis.