Autoimmune Polyglandular Syndrome (APS) Type II, A Case Report

Schmidt syndrome is a polyendocrinopathy characterized by multiple organ failures. Patients with two or more of the following characteristics are diagnosed with this syndrome: Graves' disease, adrenal insufficiency, autoimmune thyroiditis, and type I diabetes. The present case report concerns a...

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Main Authors: Narges Mirzaei Ilali, Mohammad Abedi samakoosh, Zeinab sheidai, Somayeh sheidaei
格式: 文件
语言:English
出版: Mazandaran University of Medical Sciences 2023-11-01
丛编:Journal of Mazandaran University of Medical Sciences
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在线阅读:http://jmums.mazums.ac.ir/article-1-19879-en.pdf
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author Narges Mirzaei Ilali
Mohammad Abedi samakoosh
Zeinab sheidai
Somayeh sheidaei
author_facet Narges Mirzaei Ilali
Mohammad Abedi samakoosh
Zeinab sheidai
Somayeh sheidaei
author_sort Narges Mirzaei Ilali
collection DOAJ
description Schmidt syndrome is a polyendocrinopathy characterized by multiple organ failures. Patients with two or more of the following characteristics are diagnosed with this syndrome: Graves' disease, adrenal insufficiency, autoimmune thyroiditis, and type I diabetes. The present case report concerns a Schmidt syndrome patient (polyglandular autoimmune syndrome type II). The patient is a 42-year-old woman with type I diabetes and complaints of imbalance, weakness and lethargy, weight loss, darkened skin, blood pressure drop, hypoglycemia, and hyperkalemia who visited the Hospital frequently and was discharged every time after intravenous potassium chloride and dextrose injections and orders to reduce insulin consumption at home. Her blood cortisol level was measured in her last visit with suspicion of adrenal insufficiency, which was revealed to be low (less than 0.5 μg/dL). A high ACTH, low aldosterone, and normal renin were also reported, indicating secondary adrenal insufficiency. Furthermore, T4 and TSH tests were performed, reporting a TSH lower than 0.2 in the initial TSH test, which was revealed to be normal after the test was repeated. Subclinical hyperthyroidism was indicated, given the high TRAb figure. The patient underwent treatment with fludrocortisone and prednisolone, which improved her condition. This report accentuates that diabetic patients with reduced insulin requirements must be checked for adrenal insufficiency immediately to prevent potential complications.
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spelling doaj.art-19b85efdeed54befbadf540328dc69052023-12-02T10:14:03ZengMazandaran University of Medical SciencesJournal of Mazandaran University of Medical Sciences1735-92601735-92792023-11-0133227345349Autoimmune Polyglandular Syndrome (APS) Type II, A Case ReportNarges Mirzaei Ilali0Mohammad Abedi samakoosh1Zeinab sheidai2Somayeh sheidaei3 Assistant Professor, Diabetes Research Center, Mazandaran University of Medical Sciences, Sari, Mazandaran, Iran Assistant Professor, Department of Internal Medicine, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran Assistant Professor, Diabetes Research Center, Mazandaran University of Medical Sciences, Sari, Mazandaran, Iran Assistant Professor of Pathology, Department of Pathology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran Schmidt syndrome is a polyendocrinopathy characterized by multiple organ failures. Patients with two or more of the following characteristics are diagnosed with this syndrome: Graves' disease, adrenal insufficiency, autoimmune thyroiditis, and type I diabetes. The present case report concerns a Schmidt syndrome patient (polyglandular autoimmune syndrome type II). The patient is a 42-year-old woman with type I diabetes and complaints of imbalance, weakness and lethargy, weight loss, darkened skin, blood pressure drop, hypoglycemia, and hyperkalemia who visited the Hospital frequently and was discharged every time after intravenous potassium chloride and dextrose injections and orders to reduce insulin consumption at home. Her blood cortisol level was measured in her last visit with suspicion of adrenal insufficiency, which was revealed to be low (less than 0.5 μg/dL). A high ACTH, low aldosterone, and normal renin were also reported, indicating secondary adrenal insufficiency. Furthermore, T4 and TSH tests were performed, reporting a TSH lower than 0.2 in the initial TSH test, which was revealed to be normal after the test was repeated. Subclinical hyperthyroidism was indicated, given the high TRAb figure. The patient underwent treatment with fludrocortisone and prednisolone, which improved her condition. This report accentuates that diabetic patients with reduced insulin requirements must be checked for adrenal insufficiency immediately to prevent potential complications.http://jmums.mazums.ac.ir/article-1-19879-en.pdfadrenal insufficiencyautoimmune polyglandular syndrome type iidiabeteshyperthyroidisschmidt syndrome
spellingShingle Narges Mirzaei Ilali
Mohammad Abedi samakoosh
Zeinab sheidai
Somayeh sheidaei
Autoimmune Polyglandular Syndrome (APS) Type II, A Case Report
Journal of Mazandaran University of Medical Sciences
adrenal insufficiency
autoimmune polyglandular syndrome type ii
diabetes
hyperthyroidis
schmidt syndrome
title Autoimmune Polyglandular Syndrome (APS) Type II, A Case Report
title_full Autoimmune Polyglandular Syndrome (APS) Type II, A Case Report
title_fullStr Autoimmune Polyglandular Syndrome (APS) Type II, A Case Report
title_full_unstemmed Autoimmune Polyglandular Syndrome (APS) Type II, A Case Report
title_short Autoimmune Polyglandular Syndrome (APS) Type II, A Case Report
title_sort autoimmune polyglandular syndrome aps type ii a case report
topic adrenal insufficiency
autoimmune polyglandular syndrome type ii
diabetes
hyperthyroidis
schmidt syndrome
url http://jmums.mazums.ac.ir/article-1-19879-en.pdf
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AT mohammadabedisamakoosh autoimmunepolyglandularsyndromeapstypeiiacasereport
AT zeinabsheidai autoimmunepolyglandularsyndromeapstypeiiacasereport
AT somayehsheidaei autoimmunepolyglandularsyndromeapstypeiiacasereport