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Behcet's Disease and Endocrine System
Author(s) -
Onur Özhan,
Kerem Sezer
Publication year - 2011
Publication title -
pathology research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.398
H-Index - 21
eISSN - 2090-8091
pISSN - 2042-003X
DOI - 10.1155/2012/827815
Subject(s) - medicine , behcet's disease , endocrine system , sex organ , disease , vasculitis , systemic disease , systemic vasculitis , insulin resistance , endocrine disease , adrenal insufficiency , autoimmune disease , pathology , dermatology , hormone , diabetes mellitus , endocrinology , biology , genetics
Behcet's disease (BD) is a chronic disease which is characterized by recurrent oral apthous ulcerations, recurrent genital ulcerations, skin eruptions, ocular involvements and other various systemic manifestations as well as systemic vasculitis. Endocrine involvement in BD regarding various systems can be seen. Hypophysis is one of the best and dense vascularized organs of the body, thus it is likely that it can be affected by BD. Not only anterior hypophysis functions, but posterior hypophysis functions as well can be affected. As BD is a disease of autoimmune process, it may be possible that adrenal insufficiency or alterations in the cortisol levels could be expected. Another concern is whether or not there is insulin resistance in patients with BD. The avaliable data suggests that there is an increased susceptibility to insulin resistance in patients with BD.

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