Autoimmune Polyglandular Syndrome Type 2: A Rare Condition in Childhood
Author(s) -
Heves Kırmızıbekmez,
Gül Yeşiltepe Mutlu,
Nafiye Urgancı,
Ayşe Öner
Publication year - 2015
Publication title -
journal of clinical research in pediatric endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.566
H-Index - 35
eISSN - 1308-5735
pISSN - 1308-5727
DOI - 10.4274/jcrpe.1394
Subject(s) - medicine , autoimmunity , disease , endocrine system , type 1 diabetes , autoimmune disease , endocrine disease , immunology , diabetes mellitus , endocrinology , hormone
Autoimmune polyglandular syndrome type 2 is defined as the occurrence of Addison's disease concomitantly with autoimmune thyroid disease and/or type 1 diabetes mellitus. An 11-year-old boy with Hashimoto's disease, Addison's disease, celiac disease and Langerhans islet cell autoimmunity is described in this case report. Treatment of an endocrine disease may also trigger the onset of another endocrine disease. This case report underlines the importance of early recognition and treatment of critical endocrine diseases as well as the necessity to investigate pediatric patients with autoimmune diseases for coexisting conditions. Furthermore, the role of psychological stress as an inducer of autoimmunity was also discussed.
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