MERKEL CELL TUMOR-LIKE NEUROENDOCRINE CARCINOMA-ASSOCIATED WITH THE SUBMANDIBULAR-GLAND - REPORT OF A CASE WITH CYTOLOGIC, IMMUNOHISTOCHEMICAL, ELECTRON-MICROSCOPIC AND FLOW CYTOMETRIC STUDIES
Gch. Yang et al., MERKEL CELL TUMOR-LIKE NEUROENDOCRINE CARCINOMA-ASSOCIATED WITH THE SUBMANDIBULAR-GLAND - REPORT OF A CASE WITH CYTOLOGIC, IMMUNOHISTOCHEMICAL, ELECTRON-MICROSCOPIC AND FLOW CYTOMETRIC STUDIES, Acta cytologica, 38(5), 1994, pp. 742-746
We report a rare case of primary Merkel cell tumor (MCT)-like neuroend
ocrine carcinoma (i.e., small cell carcinoma) associated with the subm
andibular gland in a 73-year-old man. Despite the lack of a known skin
primary, the tumor exhibited cytomorphologic (predominant single cell
s with ''intermediate filament buttons'' in the background), ultrastru
ctural (dense core granules and a globular aggregate of intermediate f
ilaments) and immunohistochemical (paranuclear globular coexpression o
f cytokeratin and neurofilaments) features identical to that of MCT. T
he tumor contained an aneuploid peak with DNA index of 1.1 and an S ph
ase of 20.5%. The tumor measured 5.8 cm and was situated between the s
kin and submandibular gland, with which it was closely associated brit
separated by connective tissue. The literature on MCT without a known
skin primary is reviewed, and the cytomorphologic features that allow
the distinction between MCT, lymphoma and oat cell carcinoma are disc
ussed.