Literature DB >> 19471237

Adrenal cortical tumors and multiple endocrine neoplasia-related syndromes.

M Haase1, H S Willenberg.   

Abstract

Relatively frequent, adrenal masses include a multitude of different tumor types: uni- or bilateral hyperplasias, adenomas, and the rare entity of adrenocortical carcinomas. With significant progress in our appreciation of their underlying molecular pathomechanisms and from analysis of affected individuals and their families, a number of inherited diseases and tumor syndromes have been linked to adrenocortical tumorigenesis. These syndromes and diseases include the Carney complex, the McCune-Albright syndrome, multiple endocrine neoplasia type 1, familial adenomatosis coli, congenital adrenal hyperplasia, familial forms of primary aldosteronism, the Beckwith-Wiedemann syndrome, and the Li-Fraumeni syndrome. The key to successful management of these syndromes is identification of patients harboring adrenal tumors within the context of hereditary diseases, since diagnostic procedures, therapy and follow-up may significantly differ from the management of sporadic, isolated adrenal tumors. This review explores the underlying genetic defects, diagnosis and therapy of the major heritable tumor syndromes associated with adrenocortical tumorigenesis.

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Year:  2009        PMID: 19471237

Source DB:  PubMed          Journal:  Minerva Endocrinol        ISSN: 0391-1977            Impact factor:   2.184


  1 in total

1.  Lung adenocarcinoma and adrenocortical carcinoma in a patient with multiple endocrine neoplasia type 1.

Authors:  Nobumasa Ohara; Masanori Kaneko; Masahiro Ikeda; Fumio Ishizaki; Kazuya Suzuki; Ryo Maruyama; Takeshi Komeyama; Kazuhiro Sato; Kenichi Togashi; Hiroyuki Usuda; Yuto Yamazaki; Hironobu Sasano; Kenzo Kaneko; Kyuzi Kamoi
Journal:  Respir Med Case Rep       Date:  2016-12-18
  1 in total

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