X. Matiasguiu et al., METASTATIC NEUROENDOCRINE TUMORS TO THE THYROID-GLAND MIMICKING MEDULLARY CARCINOMA - A PATHOLOGICAL AND IMMUNOHISTOCHEMICAL STUDY OF 6 CASES, The American journal of surgical pathology, 21(7), 1997, pp. 754-762
The clinical, pathological, and immunohistochemical features of six ca
ses of metastatic neuroendocrine and carcinoid tumors to the thyroid s
imulating medullary thyroid carcinoma (MTC) are described. The patient
s were women between the ages of 24 and 70 years who, without symptoms
or significant past medical histories, presented with either a single
mass or multiple thyroid nodules. The primary source of the tumor was
only discovered on follow-up. Two of the neoplasms were classical car
cinoid tumors, one was a carcinoid predominantly composed of large cel
ls, another showed a prominent oval to spindle cell component, and the
two remaining cases were atypical carcinoid/high-grade neuroendocrine
carcinomas. The immunohistochemical profile was inconsistent with MTC
in that all tumors were negative for calcitonin and only two were foc
ally positive for carcinoembryonic antigen (CEA). A variable pat tern
of staining for other neuroendocrine and epithelial markers was obtain
ed in each case. Despite the morphologic and immunohistochemical simil
arities with MTC, the diagnosis of a metastatic neuroendocrine tumor t
o the thyroid should be favored in the presence of a predominantly int
erstitial pattern of spread; occurrence of multiple tumor foci; follic
ulotropism; rosette formations with lumen and cuticular borders: and l
ack of immunoreactivity for calcitonin and CEA. The differential diagn
osis between MTC and metastatic neuroendocrine carcinoma to the thyroi
d is of importance because of the vast differences in treatment and pr
ognosis.