An Unusual Patient with Hashimoto Thyroiditis, Features of Steroid-Responsive Encephalopathy Associated with Autoimmune Thyroiditis, and Concurrent Minimal Change Renal Disease

ABSTRACT: Objective: To present an unusual patient with Hashimoto thyroiditis, encephalopathy with features of steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT), and acute kidney injury secondary to minimal change renal disease.Methods: We present clinical, laboratory,...

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Main Authors: Sandra Aleksic, MD, Hanna Oh, MD, Kalpesh G. Patel, MD, Roopa Roy, MD, Maya P. Raghuwanshi, MD, Joshua M. Kaplan, MD
Format: Article
Language:English
Published: Elsevier 2017-01-01
Series:AACE Clinical Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2376060520304144
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spelling doaj-03bae87dc7cb499c8ff45e27b49b04642021-04-30T07:24:35ZengElsevierAACE Clinical Case Reports2376-06052017-01-0134299302An Unusual Patient with Hashimoto Thyroiditis, Features of Steroid-Responsive Encephalopathy Associated with Autoimmune Thyroiditis, and Concurrent Minimal Change Renal DiseaseSandra Aleksic, MD0Hanna Oh, MD1Kalpesh G. Patel, MD2Roopa Roy, MD3Maya P. Raghuwanshi, MD4Joshua M. Kaplan, MD5From the Division of Endocrinology, Department of Medicine, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, New York; Address correspondence to Dr. Sandra Aleksic, 3444 Wayne Avenue, Endocrinology Suite, Bronx, NY 10467.Rutgers New Jersey Medical School, Newark, New Jersey.Department of Medicine, Rutgers New Jersey Medical School, Newark, New Jersey.Division of Endocrinology, Department of Medicine, Rutgers New Jersey Medical School, Newark, New Jersey.Division of Endocrinology, Department of Medicine, Rutgers New Jersey Medical School, Newark, New Jersey.Division of Nephrology and Hypertension, Department of Medicine, Rutgers New Jersey Medical School, Newark, New Jersey.ABSTRACT: Objective: To present an unusual patient with Hashimoto thyroiditis, encephalopathy with features of steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT), and acute kidney injury secondary to minimal change renal disease.Methods: We present clinical, laboratory, imaging, electroencephalography, and renal histopathologic findings, and review the relevant literature for evaluation and treatment of SREAT.Results: A 53-year-old woman with a history of hypothyroidism on levothyroxine was admitted for progressive altered mental status and bizarre behavior for 3 weeks. On exam she was lethargic with myoclonic jerks, hypertonia, and hyperreflexia. Laboratory analyses showed thyroid-stimulating hormone of 0.057 μU/mL (normal, 0.27 to 4.0 μU/mL), free thyroxine of 1.5 ng/dL (normal, 0.7 to 1.5 ng/dL), triiodothyronine of 0.7 ng/mL (normal, 0.6 to 1.6 ng/dL), and elevated anti–thyroid peroxidase (>600 U/L) and antithyroglobulin (57.2 U/L) antibodies. The patient failed to improve with empiric antibiotics and anticonvulsants. She developed oliguric acute kidney injury with proteinuria requiring hemodialysis. Renal biopsy was consistent with minimal change disease and acute tubular necrosis. Further workup failed to identify infectious, structural, toxic, or neoplastic causes of the encephalopathy. SREAT was suspected and the patient was started on high-dose steroid therapy. Both the patient's mental status and renal function significantly improved with steroids and she was discharged home.Conclusion: We present, to our knowledge, the first case of Hashimoto thyroiditis associated with both encephalopathy with features of SREAT and minimal change renal disease. SREAT should be suspected in a patient with Hashimoto thyroiditis and unexplained encephalopathy that fails to respond to treatment.Abbreviations: anti-TPO anti–thyroid peroxidase; CNS central nervous system; CSF cerebrospinal fluid; fT4 free thyroxine; MRI magnetic resonance imaging; SREAT steroid-responsive encephalopathy associated with autoimmune thyroiditis; T3 triiodothyronine; TSH thyroid-stimulating hormonehttp://www.sciencedirect.com/science/article/pii/S2376060520304144
collection DOAJ
language English
format Article
sources DOAJ
author Sandra Aleksic, MD
Hanna Oh, MD
Kalpesh G. Patel, MD
Roopa Roy, MD
Maya P. Raghuwanshi, MD
Joshua M. Kaplan, MD
spellingShingle Sandra Aleksic, MD
Hanna Oh, MD
Kalpesh G. Patel, MD
Roopa Roy, MD
Maya P. Raghuwanshi, MD
Joshua M. Kaplan, MD
An Unusual Patient with Hashimoto Thyroiditis, Features of Steroid-Responsive Encephalopathy Associated with Autoimmune Thyroiditis, and Concurrent Minimal Change Renal Disease
AACE Clinical Case Reports
author_facet Sandra Aleksic, MD
Hanna Oh, MD
Kalpesh G. Patel, MD
Roopa Roy, MD
Maya P. Raghuwanshi, MD
Joshua M. Kaplan, MD
author_sort Sandra Aleksic, MD
title An Unusual Patient with Hashimoto Thyroiditis, Features of Steroid-Responsive Encephalopathy Associated with Autoimmune Thyroiditis, and Concurrent Minimal Change Renal Disease
title_short An Unusual Patient with Hashimoto Thyroiditis, Features of Steroid-Responsive Encephalopathy Associated with Autoimmune Thyroiditis, and Concurrent Minimal Change Renal Disease
title_full An Unusual Patient with Hashimoto Thyroiditis, Features of Steroid-Responsive Encephalopathy Associated with Autoimmune Thyroiditis, and Concurrent Minimal Change Renal Disease
title_fullStr An Unusual Patient with Hashimoto Thyroiditis, Features of Steroid-Responsive Encephalopathy Associated with Autoimmune Thyroiditis, and Concurrent Minimal Change Renal Disease
title_full_unstemmed An Unusual Patient with Hashimoto Thyroiditis, Features of Steroid-Responsive Encephalopathy Associated with Autoimmune Thyroiditis, and Concurrent Minimal Change Renal Disease
title_sort unusual patient with hashimoto thyroiditis, features of steroid-responsive encephalopathy associated with autoimmune thyroiditis, and concurrent minimal change renal disease
publisher Elsevier
series AACE Clinical Case Reports
issn 2376-0605
publishDate 2017-01-01
description ABSTRACT: Objective: To present an unusual patient with Hashimoto thyroiditis, encephalopathy with features of steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT), and acute kidney injury secondary to minimal change renal disease.Methods: We present clinical, laboratory, imaging, electroencephalography, and renal histopathologic findings, and review the relevant literature for evaluation and treatment of SREAT.Results: A 53-year-old woman with a history of hypothyroidism on levothyroxine was admitted for progressive altered mental status and bizarre behavior for 3 weeks. On exam she was lethargic with myoclonic jerks, hypertonia, and hyperreflexia. Laboratory analyses showed thyroid-stimulating hormone of 0.057 μU/mL (normal, 0.27 to 4.0 μU/mL), free thyroxine of 1.5 ng/dL (normal, 0.7 to 1.5 ng/dL), triiodothyronine of 0.7 ng/mL (normal, 0.6 to 1.6 ng/dL), and elevated anti–thyroid peroxidase (>600 U/L) and antithyroglobulin (57.2 U/L) antibodies. The patient failed to improve with empiric antibiotics and anticonvulsants. She developed oliguric acute kidney injury with proteinuria requiring hemodialysis. Renal biopsy was consistent with minimal change disease and acute tubular necrosis. Further workup failed to identify infectious, structural, toxic, or neoplastic causes of the encephalopathy. SREAT was suspected and the patient was started on high-dose steroid therapy. Both the patient's mental status and renal function significantly improved with steroids and she was discharged home.Conclusion: We present, to our knowledge, the first case of Hashimoto thyroiditis associated with both encephalopathy with features of SREAT and minimal change renal disease. SREAT should be suspected in a patient with Hashimoto thyroiditis and unexplained encephalopathy that fails to respond to treatment.Abbreviations: anti-TPO anti–thyroid peroxidase; CNS central nervous system; CSF cerebrospinal fluid; fT4 free thyroxine; MRI magnetic resonance imaging; SREAT steroid-responsive encephalopathy associated with autoimmune thyroiditis; T3 triiodothyronine; TSH thyroid-stimulating hormone
url http://www.sciencedirect.com/science/article/pii/S2376060520304144
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