M. Sierra et al., ANAPLASTIC CARCINOMA OF THE THYROID AT TH E NSTITUTO-NACIONAL-DE-LA-NUTRICION-SALVADOR-ZUBIRAN, Revista de Investigacion Clinica, 49(2), 1997, pp. 97-103
Background. Anaplastic thyroid carcinoma (ATC) is a highly aggressive
tumor with a median survival rate of 6 months. Aim. To analyze present
ation, treatment, morphology, immunohistochemistry, and nuclear DNA an
alysis of a cohort of patients with ATC. Patients and methods. Twelve
patients with ATC (11 female) with a mean age of 65 years were seen at
our hospital from 1970-1995. The data were obtained from the clinical
records and the morphology, immunohistochemic studies and DNA pattern
were performed in slides obtained from archival specimens. Results. P
revious or coexisting thyroide disease was documented in 10 patients (
9 multinodular goiters and one Grave's). The most frequent presentatio
n was a rapidly growing tumor associated with dysphagia, cervical pain
, hoarseness and dyspnea. A cold thyroid nodule was detected by thyroi
d scan in 10 patients. The most frequent subtype was the spindle cell
variety. Papillary thyroid carcinoma coexisted in eight cases, two of
them corresponded to the tall cell variant. Reactivity for S-100 prote
in and vimentin was studied in six patients: all were positive for S-1
00 protein and vimentin, 5/6 for epithelial membrane antigen, half for
carcinoembriogenic antigen, 2/6 for thyroglobulin and calcitonin, and
one for neuronal specific enolase. These six tumors showed a diploid
DNA pattern. Tumor resection was achieved in 2/11 and none survived si
x years after diagnosis. Conclusions. ATC is a highly aggressive tumor
coexisting with thyroid pathologies. Spindle cell variant is the most
frequent with positive reactivity for S-100 protein, vimentin and epi
thelial membrane antigen. Most tumors have a diploid DNA content.