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Autoimmune Polyglandular Syndrome II: A Case Report.
Awad, Olfat; Basma, Hadil; Masri, Rim; Hamadeh, Samih; Hamadeh, Majdi.
Afiliación
  • Awad O; Department of Nephrology, Lebanese University Faculty of Medical Sciences, Beirut, LBN.
  • Basma H; Department of Endocrinology, Lebanese University Faculty of Medical Sciences, Beirut, LBN.
  • Masri R; Department of Endocrinology, Lebanese University Faculty of Medical Sciences, Beirut, LBN.
  • Hamadeh S; Department of Internal Medicine, Wayne State University Detroit Medical Center, Detroit, USA.
  • Hamadeh M; Department of Nephrology, Lebanese University Faculty of Medical Sciences, Beirut, LBN.
Cureus ; 16(1): e52372, 2024 Jan.
Article en En | MEDLINE | ID: mdl-38361732
ABSTRACT
Autoimmune polyglandular syndrome II (APS-II), also known as Schmidt syndrome, is a rare endocrine disorder characterized by endocrine and non-endocrine illnesses. Addison's disease and at least one additional autoimmune condition, such as autoimmune thyroid disease or type 1 diabetes mellitus (T1DM), are features of APS-II. It can result from genetic and non-genetic factors. We present a case of a 60-year-old female patient with a history of T1DM and a recent diagnosis of Hashimoto's thyroiditis who was admitted to the nephrology department for hyponatremia. Investigations showed the presence of adrenal insufficiency (AI), so she was diagnosed with APS-II and had the full triad of this syndrome. Thus, it is important to think about the diagnosis of AI or other autoimmune conditions in a patient who already has one or more autoimmune diseases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cureus Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cureus Año: 2024 Tipo del documento: Article