Autoimmune Polyglandular Syndrome type 2
| العنوان: | Autoimmune Polyglandular Syndrome type 2 |
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| المؤلفون: | Luís Costa Matos, João Olivério, Mónica Teixeira, Sofia Costa Martins, Gabriela Venade, João Machado, Joana Silva Marques |
| المصدر: | Revista da Associação Médica Brasileira, Vol 65, Iss 12, Pp 1434-1437 (2020) Revista da Associação Médica Brasileira, Volume: 65, Issue: 12, Pages: 1434-1437, Published: 24 JAN 2020 |
| بيانات النشر: | Associação Médica Brasileira, 2020. |
| سنة النشر: | 2020 |
| مصطلحات موضوعية: | Adult, medicine.medical_specialty, Medicine (General), endocrine system diseases, Fludrocortisone, 030204 cardiovascular system & hematology, Hypoglycemia, Gastroenterology, Doenças da glândula tireoide, 03 medical and health sciences, Poliendocrinopatias autoimunes, Rare Diseases, 0302 clinical medicine, R5-920, Addison Disease, Internal medicine, medicine, Humans, Doença de Addison, 030212 general & internal medicine, Polyendocrinopathies, Autoimmune, Autoimmune disease, Type 1 diabetes, business.industry, Type 2 Diabetes Mellitus, General Medicine, medicine.disease, Thyroid Diseases, Graves Disease, Early Diagnosis, Treatment Outcome, Diabetes Mellitus, Type 1, Diabetes mellitus tipo 1, Addison's disease, Prednisolone, Autoimmune Polyglandular Syndrome Type 2, Female, business, Addison’s Disease, medicine.drug |
| الوصف: | SUMMARY Autoimmune polyglandular syndrome type 2 (APS 2) is defined by the presence of Addison’s disease (AD) associated with autoimmune thyroid disease and/or Type 1 diabetes mellitus (T1DM). It is a rare disease, affecting about 1.4-2 cases/100,000 inhabitants. Its less frequent clinical presentation is the combination of AD, Graves‘ disease, and T1DM. We present the case of a 42-year-old woman with a history of total thyroidectomy due to Graves’ disease, type 2 diabetes mellitus, and hypertension, who sought the ED due to asthenia, dizziness, nausea, and vomiting. She reported having stopped antihypertensive therapy due to hypotension and presented a glycemic record with frequent hypoglycemia. On physical examination, she had cutaneous hyperpigmentation. She had no leukocytosis, anemia, hypoglycemia, hyponatremia or hyperkalemia, and a negative PCR. Serum cortisol |
| وصف الملف: | text/html |
| اللغة: | English |
| تدمد: | 1806-9282 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::248afd7af3b11b47970f8e068dc8af8fTest http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302019001201434&tlng=enTest |
| حقوق: | OPEN |
| رقم الانضمام: | edsair.doi.dedup.....248afd7af3b11b47970f8e068dc8af8f |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 18069282 |
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