Pheochromocytoma associated with neuroendocrine carcinoma: A new type of composite pheochromocytoma Review uri icon

Overview

MeSH Major

  • Adrenal Gland Neoplasms
  • Carcinoma
  • Neuroendocrine Tumors
  • Pheochromocytoma

abstract

  • The coexistence of pheochromocytoma and other tumor types in a single adrenal gland has been rarely documented. This type of pheochromocytoma is designated "composite" or "mixed," depending on whether the pheochromocytoma and the nonpheochromocytoma components show the same embryologic origin. The nonpheochromocytoma components reported in the composite pheochromocytoma include ganglioneuroma, ganglioneuroblastoma, neuroblastoma, and malignant schwannoma. The components found in the mixed pheochromocytoma include adrenal cortical neoplasms and spindle cell sarcoma. We report a unique case of composite pheochromocytoma in which the nonpheochromocytoma element is a neuroendocrine carcinoma. The histologic and the immunohistochemical profiles of the 2 distinct components of this tumor were typical for those of pheochromocytoma and neuroendocrine carcinoma. This dual differentiation was also supported by ultrastructural findings. This case not only broadens the morphologic spectrum of composite pheochromocytoma but also provides some additional insight into the histogenesis of this rare but fascinating type of tumor.

publication date

  • December 21, 1999

Research

keywords

  • Review

Identity

Language

  • eng

PubMed ID

  • 10583935

Additional Document Info

start page

  • 1274

end page

  • 9

volume

  • 123

number

  • 12