Kw. Min, GANGLIOCYTIC PARAGANGLIOMA OF THE DUODENUM - REPORT OF A CASE WITH IMMUNOCYTOCHEMICAL AND ULTRASTRUCTURAL INVESTIGATION, Ultrastructural pathology, 21(6), 1997, pp. 587-595
A case of gangliocytic paraganglioma is reported in a 70-year-old fema
le presenting as a polypoid tumor of the second portion of the duodenu
m. Immunohistochemical and ultrastructural features of the tumor indic
ate that gangliocytic paraganglioma of the duodenum (GPD) represents a
n unique tumor originating from the neuroectodermal derivative exhibit
ing dual phenotypic expression toward paraganglionic and epithelial (n
euroendocrine) cells. These findings correlate well with the literatur
e and it is further suggested that GPD belongs to the histopathologic
spectrum of tumors derived from the neural crest. The findings offer a
plausible explanation for histogenetic genetic possibilities of the o
ccurrence of pure epithelial tumors (i.e., carcinoid-like tumors) in t
he paraganglionic systems. The patient remains with no evidence of dis
ease 4 years following a simple polypectomy.