A concise genetic and clinical guide to multiple endocrine neoplasias and related syndromes

Constantine A. Stratakis, Douglas W Ball

Research output: Contribution to journalArticle

Abstract

Several familial neoplastic syndromes are associated with endocrine gland oncogenesis. The main ones are: multiple endocrine neoplasia type 1 (MEN 1), which affects primarily the pituitary, pancreas, and parathyroid glands; MEN 2A and MEN 2B, which involve mainly the thyroid and parathyroid glands and the adrenal medulla; familial medullary thyroid carcinoma (FMTC), which affects only the thyroid gland; and, finally, Carney complex, which affects the adrenal cortex, pituitary, thyroid gland, and the gonads. Carney complex is also associated with pigmentation abnormalities and myxoid and other neoplasms of mesenchymal origin. Thus, this syndrome also belongs to another group of genetic disorders, those associated with pigmentation defects and multiple tumors, including tumors of the endocrine glands. Peutz- Jeghers syndrome and Cowden disease are just two of these disorders that have recently been elucidated at the molecular level. von Hippel-Lindau disease is another condition that affects the pancreas and adrenal medulla and its gene is also known. The inheritance of the MENs, Carney complex, and related syndromes is autosomal dominant. Clinical recognition of these syndromes at a young age improves clinical outcome and prognosis of the various tumors and decreases associated morbidity and mortality. This review considers a wider, more inclusive view of the MEN syndromes, summarizes their clinical features and presents the newest information on their molecular elucidation.

Original languageEnglish (US)
Pages (from-to)457-465
Number of pages9
JournalJournal of Pediatric Endocrinology and Metabolism
Volume13
Issue number5
StatePublished - 2000

Fingerprint

Multiple Endocrine Neoplasia
Carney Complex
Endocrine Glands
Thyroid Gland
Adrenal Medulla
Parathyroid Glands
Pigmentation
Pituitary Gland
Pancreas
Neoplasms
Multiple Endocrine Neoplasia Type 2b
Multiple Hamartoma Syndrome
Peutz-Jeghers Syndrome
Multiple Endocrine Neoplasia Type 2a
von Hippel-Lindau Disease
Multiple Endocrine Neoplasia Type 1
Inborn Genetic Diseases
Adrenal Cortex
Gonads
Carcinogenesis

Keywords

  • Carney complex
  • Cowden disease
  • Hamartomatoses
  • Lentiginosis
  • Multiple endocrine neoplasia syndromes
  • Peutz-Jeghers syndrome

ASJC Scopus subject areas

  • Endocrinology
  • Pediatrics, Perinatology, and Child Health

Cite this

A concise genetic and clinical guide to multiple endocrine neoplasias and related syndromes. / Stratakis, Constantine A.; Ball, Douglas W.

In: Journal of Pediatric Endocrinology and Metabolism, Vol. 13, No. 5, 2000, p. 457-465.

Research output: Contribution to journalArticle

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