Background and aim: Despite a variety of diagnostic tools, diagnosis of thy
roid carcinoma remains difficult. A differentiation between benign and mali
gnant thyroid diseases is however essential for operative decision making.
The aim our study was to investigate a nested RT-PCR system to detect Cytok
eratin 20 (CK 20) in benign and malignant thyroid tissues and peripheral bl
ood.
Methods: Frozen tissue sections of 33 thyroid carcinomas and 30 benign thyr
oid diseases (14 multinodular goiters, 14 follicular adenomas, 2 Hashimoto'
s thyroiditis) were obtained intraoperatively. Blood samples were drawn fro
m 27 patients with thyroid carcinomas, 9 patients with benign thyroid disea
ses and 7 healthy volunteers.
Results: 100% of the medullary, 70% of the follicular, 27% of the papillary
and 25% of the anaplastic carcinomas showed an expression of CR 20 mRNA in
the examined frozen tissue sections. CK 20 mRNA was undetectable in 30 ben
ign thyroid diseases. Circulating tumor cells were found in the peripheral
blood of 2/4 patients with medullary, 2/7 with follicular, 1/13 patients wi
th papillary and 1/3 patients with anaplastic thyroid carcinomas. CK 20 mRN
A could not be detected in blood samples of patients with benign thyroid di
seases and healthy volunteers.
Conclusion: CK 20 transcripts can be detected sucessfully in tissue section
s of thyroid carcinomas but not in benign thyroid diseases. Moreover the in
vestigated CK 20 RT-PCR system is able to detect circulating tumor cells of
thyroid carcinomas in the peripheral blood.