Gangliocytic Paraganglioma of the Duodenum: Report of a Case with Immunocytochemical and Ultrastructural Investigation

References

• Kepes JJ, Zacharias DL. Gangliocytic paragangliomas of the duodenum: a report of two cases with light and electron microscopic examination. Cancer 1971; 27: 61–70
   PubMedGoogle Scholar
• Burke AP, Helwig EB. Gangliocytic paraganglioma. Am J Clin Pathol. 1989; 92: 1–9
   PubMed Web of Science ®Google Scholar
• Reed RJ, Caroca PJ, Jr, Harkin JC. Gangliocytic paraganglioma. Am J Surg Pathol. 1977; 1: 207–216
   PubMed Web of Science ®Google Scholar
• Perrone T, Sibley RK, Rosai J. Duodenal gangliocytic paraganglioma: an immunohistochemical and ultrastructural study and a hypothesis concerning its origin. Am J Surg Pathol. 1985; 9: 31–41
   PubMedGoogle Scholar
• Hamid QA, Bishop AE, Rode J, et al. Duodenal gangliocytic paragangliomas: a study of 10 cases with immunocytochemical neuroendocrine markers. Hum Pathol. 1986; 17: 1151–1157
   PubMed Web of Science ®Google Scholar
• Scheithauer BW, Nora FE, Lechargo J, et al. Duodenal gangliocytic paraganglioma: clinicopathologic and immunocytochemical study of 11 cases. Am J Clin Pathol. 1986; 86: 559–565
   PubMedGoogle Scholar
• Lloyd RV, Blaivas M, Wilson BS. Distribution of chromogranin and S-100 protein in normal and abnormal adrenal medullary tissues. Arch Pathol Lab Med. 1985; 109: 633–635
   PubMed Web of Science ®Google Scholar
• Capella C, Riva C, Cornaggia M, Chiaravalli AM, Frigerio B. Histopathology, cytology and cytochemistry of pheochromocytomas and paragangliomas including chemodectomas. Pathol Res Pract. 1988; 183: 176–187
   PubMed Web of Science ®Google Scholar
• Schroder HD, Johannsen L. Demonstration of S-100 protein in sustentacular cells of pheochromocytomas and paragangliomas. Histopathology 1986; 10: 1023–1033
   PubMed Web of Science ®Google Scholar
• Ironside JW, Royds JA, Taylor CB, Timperly WR. Paraganglioma of cauda equina: a histological, ultrastructural and immunohistochemical study of two cases with a review of the literature. J Pathol. 1985; 145: 195–201
   PubMed Web of Science ®Google Scholar
• Hirose T, Sano T, Mori K, et al. Paraganglioma of the cauda equina: an ultrastructural and immunohistochemical study of two cases. Ultrastruct Pathol. 1988; 12: 235–243
   PubMed Web of Science ®Google Scholar
• Johnson TL, Zarbo RJ, Lloyd RV, Crissman JD. Paragangliomas of the head and neck: immunohistochemical neuroendocrine and intermediate filament typing. Mod Pathol. 1988; 1: 216–223
   PubMedGoogle Scholar
• Perrone T. Duodenal gangliocytic paraganglioma and carcinoid (Letter to the Editor). Am J Surg Pathol. 1986; 10: 147–150
   PubMedGoogle Scholar
• van Campenhaut E. Etude sur le development et la signification morphologique des ilots endocrines du pancreas chez I'embryon de mouton. Arch Biol (Liege) 1925; 35: 45–88
   Google Scholar
• van Campenhaut E. Contribution a I'etude de I'histogenese du pancreas chez quelques mammiferes: Ie complexes sympathico-insulares. Arch Biol (Liege) 1927; 37: 121–171
   Google Scholar
• van Campenhaut E. Contribution au probleme des connexions neuro-entoblastiques. Acad R Med Belg. 1940; 5: 189–201
   Google Scholar
• LeDouarin MN. The Neural Crest. Cambridge University Press, London 1982
   Google Scholar
• Serbedzija GN, Bronner-Fraser M, Fraser SE. Developmental potential of trunk neural crest cells in the mouse. Development 1994; 120: 1709–1718
   PubMed Web of Science ®Google Scholar
• Tsokos M, Scarpa S, Ross RA, Triche TJ. Differentiation of human neuroblastoma recapitulates neural crest development: study of morphology, neurotransmitter enzymes and extracellular matrix proteins. Am J Pathol. 1987; 128: 484–496
   PubMed Web of Science ®Google Scholar
• Rettig WJ, Spengler BA, Chesa PG, Old LJ, Biedler JA. Coordinate changes in neuronal phenotype and surface antigen expression in human neuroblastoma cell variants. Cancer Res. 1987; 47: 1383–1389
   PubMed Web of Science ®Google Scholar
• Ogita S, Tokiwa K, Arizono N, Takahashi T. Neuroblastoma: incomplete differentiation on the way to maturation or morphologic alteration resembling maturity. Oncology 1988; 45: 148–152
   PubMed Web of Science ®Google Scholar
• Cooper MJ, Hutchins GM, Cohen PS, Helman LJ, Mennie RJ, Israel MA. Human neuroblastoma tumor cell lines correspond to the arrested differentiation of chromaffin adrenal medullary neuroblasts. Cell Growth Diff. 1990; 1: 149–159
   PubMedGoogle Scholar
• Sugimoto T, Ueyama H, Hosoi H, et al. Alpha-smooth-muscle actin and desmin expressions in human neuroblastoma cell lines. Int J Cancer 1991; 48: 227–283
   PubMedGoogle Scholar
• Bove KE, McAdams AJ. Composite ganglioneuroblastoma. Arch Pathol Lab Med. 1981; 105: 324–330
   Google Scholar
• Kragel PJ, Johnston CA. Pheochromocytoma-ganglioneuroma of the adrenal. Arch Pathol Lab Med. 1981; 109: 470–472
   Google Scholar
• Min K-W, Clemens A, Bell J, Dick H. Malignant peripheral nerve sheath tumor and pheochromocytoma: a composite tumor of the adrenal. Arch Pathol Lab Med. 1988; 112: 266–270
   PubMed Web of Science ®Google Scholar
• Holiman JL, Rosenblum Wl. Gangliorhabdomyosarcoma: a tumor of ectomesenchyme. J Neurosurg. 1971; 34: 417–422
   PubMedGoogle Scholar
• Woodruff JM. Peripheral nerve sheath tumors showing glandular differentiation (glandular schwannomas). Cancer 1976; 37: 2399–2413
   PubMed Web of Science ®Google Scholar
• Yousem SA, Colby TV, Urich H. Malignant epithelioid schwannoma arising in a benign schwannoma. Cancer 1981; 55: 2799–2803
   Google Scholar
• Arnesjo B, Idvall I, Ihse I, Telenius M, Tylen U. Concomitant occurrence of neurofibromatosis and carcinoid of the intestine. Scand J Gastroenterol. 1973; 8: 637–643
   PubMed Web of Science ®Google Scholar
• Stamm B, Hedinger CE, Saremaslani P. Duodenal and ampullary carcinoid tumors: a report of 12 cases with pathological characteristics, polypeptide content and relation to the MEN I syndrome and von Recklinghausen's disease (neurofibromatosis). Virchows Arch [A] 1986; 408: 475–489
   Google Scholar
• Griffiths DFR, Williams GT, Williams ED. Duodenal carcinoid tumors, pheochromocytoma and neurofibromatosis: islet cell tumor, pheochromocytoma and von Hippel-Lindau complex: two distinctive neuroendocrine syndromes. Quart J Med. 1987; 245: 769–782
   Google Scholar
• Llena JF, Wisoff HS, Hirano A. Gangliocytic paraganglioma in cauda equina region with biochemical and neuropathological studies. J Neurosurg. 1982; 56: 280–282
   PubMedGoogle Scholar
• Sonneland PRL, Scheithauer BW, Lechago J, Crawford BG, Onfrio BM. Paraganglioma of the cauda equina region: clinicopathologic study of 31 cases with special reference to immunocytology and ultrastructure. Cancer 1986; 58: 1720–1735
   PubMed Web of Science ®Google Scholar
• Capella C, Gabrielli M, Polak JM, Butta R, Solcia E, Bordi C. Ultrastructural and histochemical study of 11 bronchial carcinoids. Virchows Arch [A] 1979; 381: 313–329
   PubMedGoogle Scholar
• Barbareschi M, Frigo B, Mosca L, et al. Bronchial carcinoids with S-100 positive sustentacular cells: a comparative study with gastrointestinal carcinoids, pheochromocytomas and paragangliomas. Pathol Res Pract. 1990; 186: 212–222
   PubMed Web of Science ®Google Scholar
• Carlson JA, Dickersin GR. Melanotic paraganglioid carcinoid tumor: a case report and review of the literature. Ultrastruct Pathol. 1993; 17: 353–372
   PubMed Web of Science ®Google Scholar