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Steroid-Responsive Encephalopathy Associated With Autoimmune Thyroiditis Masquerading Sepsis
Jonathan Estaris1, Surbhi Bansil1, Yoshito Nishimura1
1Medicine, University of Hawaii John A. Burns School of Medicine, Honolulu, USA.
Cureus
|June 12, 2023
Summary
Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) is a rare neurological condition. Early diagnosis and treatment with steroids can lead to significant recovery in affected patients.
Area of Science:
- Neurology
- Immunology
- Endocrinology
Background:
- Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) is a rare autoimmune neurological disorder.
- It is characterized by fluctuating encephalopathy and elevated antithyroid antibodies.
Observation:
- A 72-year-old male presented with fever and altered mental status, initially suspected as sepsis.
- The patient experienced seizures and neurological decline despite initial treatment.
Findings:
- Extensive workup revealed anti-thyroid peroxidase antibodies, leading to a diagnosis of SREAT.
- The patient demonstrated significant improvement following treatment with glucocorticoids and intravenous immunoglobulins.
Implications:
- SREAT should be considered in the differential diagnosis of unexplained encephalopathy.
- Detection of antithyroid antibodies is crucial for diagnosing SREAT.
- Prompt treatment can lead to favorable neurological outcomes.
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