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A Case of Steroid-Responsive Encephalopathy
Alona Kondramashin1, Asia Filatov1, Jonathan T Grossman1
1Neurology, Florida Atlantic University Charles E. Schmidt College of Medicine, Boca Raton, USA.
Hashimoto's encephalopathy, an autoimmune thyroiditis complication, presents with gradual neurological symptoms. Prompt steroid treatment can effectively manage this steroid-responsive encephalopathy.
Area of Science:
- Neurology
- Immunology
- Endocrinology
Background:
- Hashimoto's encephalopathy (HE) is a rare neurological disorder linked to autoimmune thyroiditis.
- It typically manifests with gradual onset neurological symptoms over months.
Observation:
- The case involved a 74-year-old male with abrupt confusion.
- Diagnosis required identifying elevated anti-thyroid antibodies (anti-TPO or anti-M).
- Other findings included elevated ESR, liver enzymes, and CSF protein.
Findings:
- HE symptoms encompass cognitive decline, psychiatric disturbances, and motor deficits.
- Thyroid function tests and antibody titers do not correlate with disease severity.
- Cerebral imaging is often unremarkable.
Implications:
- Early diagnosis of HE is crucial for timely intervention.
- Steroids, IVIg, or plasmapheresis are effective treatments for HE.
- This case highlights the importance of considering autoimmune thyroiditis in encephalopathy presentations.
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