Multiple endocrine neoplasia type 2. Clinical features and screening

Endocrinol Metab Clin North Am. 1994 Mar;23(1):137-56.

Abstract

Prospective screening programs have changed the presenting clinical features of MEN 2, the association of medullary thyroid carcinoma, pheochromocytoma, and parathyroid disease. Currently, all manifestations of MEN 2 syndrome can be diagnosed at an early stage. Gene carrier status can be identified by characterization of specific mutations. Prospective screening for early medullary thyroid carcinoma by calcitonin testing and for pheochromocytoma by several techniques routinely permits identification of early manifestations.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adrenal Gland Neoplasms / diagnosis
  • Humans
  • Incidence
  • Mass Screening / methods*
  • Multiple Endocrine Neoplasia / classification
  • Multiple Endocrine Neoplasia / diagnosis*
  • Multiple Endocrine Neoplasia / genetics
  • Multiple Endocrine Neoplasia / therapy
  • Pheochromocytoma / diagnosis
  • Prognosis
  • Quality of Life
  • Thyroid Neoplasms / diagnosis