Reference : Familial pituitary adenomas.
Scientific journals : Article
Human health sciences : Endocrinology, metabolism & nutrition
http://hdl.handle.net/2268/62844
Familial pituitary adenomas.
English
Tichomirowa, M. A. [> > > >]
Daly, Adrian [Université de Liège - ULg > Département des sciences cliniques > Endocrinologie >]
Beckers, Albert mailto [Université de Liège - ULg > Département des sciences cliniques > Endocrinologie >]
Jul-2009
Journal of Internal Medicine
Blackwell Publishing
266
1
5-18
Yes (verified by ORBi)
International
0954-6820
1365-2796
Oxford
UK
[en] Cell Transformation, Neoplastic/genetics ; Female ; Humans ; Male ; Multiple Endocrine Neoplasia Type 1/genetics ; Mutation ; Neoplastic Syndromes, Hereditary/genetics ; Pituitary Neoplasms/genetics
[en] The majority of pituitary adenomas occur sporadically, however, about 5% of all cases occur in a familial setting, of which over half are due to multiple endocrine neoplasia type 1 (MEN-1) and Carney's complex (CNC). Since the late 1990s we have described non-MEN1/CNC familial pituitary tumours that include all tumour phenotypes, a condition named familial isolated pituitary adenomas (FIPA). The clinical characteristics of FIPA vary from those of sporadic pituitary adenomas, as patients with FIPA have a younger age at diagnosis and larger tumours. About 15% of FIPA patients have mutations in the aryl hydrocarbon receptor interacting protein gene (AIP), which indicates that FIPA may have a diverse genetic pathophysiology. This review describes the clinical features of familial pituitary adenomas like MEN1, the MEN 1-like syndrome MEN-4, CNC, FIPA, the tumour pathologies found in this setting and the genetic/molecular data that have been recently reported.
Researchers ; Professionals
http://hdl.handle.net/2268/62844
10.1111/j.1365-2796.2009.02109.x

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