101. Duodenal periampullary gangliocytic paraganglioma: report of two cases with immunohistochemical and ultrastructural study.
- Author
-
Altavilla G, Chiarelli S, and Fassina A
- Subjects
- Adult, Chromogranin A, Chromogranins analysis, Cytoplasmic Granules ultrastructure, Endoplasmic Reticulum ultrastructure, Female, Humans, Intestinal Mucosa pathology, Intestinal Neoplasms chemistry, Intestinal Neoplasms ultrastructure, Lysosomes ultrastructure, Male, Middle Aged, Mitochondria ultrastructure, Neurofibrils ultrastructure, Paraganglioma chemistry, Paraganglioma ultrastructure, S100 Proteins analysis, Synaptophysin analysis, Duodenum, Immunohistochemistry, Intestinal Neoplasms diagnosis, Microscopy, Electron, Paraganglioma diagnosis
- Abstract
We report two cases of Gangliocytic Paraganglioma (GP) of the ampulla of Vater occurring in a 63-year-old and a 34-year-old individual. The patients were both admitted for a long history of intermittent gastrointestinal bleeding and abdominal discomfort, with no other symptoms. At endoscopy, the GP appeared as a polypoid, ulcerated mass in the ampullar region, measuring 2.5x1.8 and 2 cm, respectively. Microscopically, the tumors showed similar features and were composed of epithelial cells (more than 50%), spindle cells, and ganglion-like cells. The epithelial cells showed clear cytoplasm and formed nests (zellballen or paraganglioma-like groups), and less frequently, cords (carcinoid-like), extending to mucosa and submucosa. Ganglion cells were sparse, constantly associated with the spindle cells. Both epithelial and ganglion cells were synaptophysin, chromogranin A, and anti-neurofilament immunoreactive. The spindle cells were all S-100 positive. Ultrastructural studies revealed dark and light cells, rare elongated cellular processes, secretory granules, and fine fibrils resembling neurofilaments. The histogenesis of GP is still a matter of debate, however its neoplastic nature is supported by the occasionally reported malignant evolution.
- Published
- 2001
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