Type II Autoimmune Polyglandular Syndrome, about a case
Keywords:
Addison's disease, Celiac Disease, Autoimmune Polyglandular SyndromeAbstract
Introduction: autoimmune Polyglandular Syndrome is characterized by the presence in the same patient of endocrine glandular insufficiencies. Presentation of the case: a 33-year-old female patient who has presented type 1 Diabetes Mellitus since she was 16 years old and generalized asthenia for 2 years. He went to the health service for presenting symptoms that corresponded to a urinary tract infection, he was admitted to the Internal Medicine service room for treatment, where the symptoms of marked decay, diarrhea, weight loss, hypotension and hypoglycemia, vitiligo and areas of melanoderma, as well as intestinal alabsorption symptoms. Conclusions: the presentation of the clinical case allows us to understand the long-term follow-up of patients with autoimmune polyglandular syndrome, which guarantees early diagnosis and timely replacement treatment of other diseases that arise in the evolution of said syndrome.
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