Autoimmune encephalitis with autoimmune myocarditis

Autoimmune encephalitis can be associated with other autoimmune disorders, but the concurrent presence of autoimmune encephalitis and autoimmune myocarditis is uncommon. A man in his 80s with type 2 diabetes mellitus, hypertension and hypothyroidism presented with altered mental status for 8 months. He was previously diagnosed with myasthenia gravis, but therapy was discontinued due to infection. On presentation, he was wheelchair-bound with disorientation, proximal weakness, hyporeflexia and bradykinesia. MRI brain showed atrophy, and cerebrospinal fluid analysis revealed mildly elevated protein (58.8 mg/dL) without pleocytosis. Despite treatment for urinary tract infection and septic encephalopathy, his sensorium did not improve. A diagnosis of possible autoimmune encephalitis was considered, though antibody studies were negative. Whole-body Positron Emission Tomography - Computerized Tomography (PET-CT) ruled out malignancy and showed global hypokinesia, while echocardiography showed severe left ventricular systolic dysfunction. Positive acetylcholine receptor antibody led to intravenous immunoglobulin therapy, which improved his sensorium and cardiac dysfunction suggesting a positive association.

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Publication Details

Journal
BMJ Case Reports
Published
2025-04-01
DOI
https://doi.org/10.1136/bcr-2025-264794
Primary Topic
Autoimmune Neurological Disorders and Treatments
Type
article
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Autoimmune encephalitis with autoimmune myocarditis

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BMJ Case Reports
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Autoimmune encephalitis with autoimmune myocarditis

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article en

Abstract

Autoimmune encephalitis can be associated with other autoimmune disorders, but the concurrent presence of autoimmune encephalitis and autoimmune myocarditis is uncommon. A man in his 80s with type 2 diabetes mellitus, hypertension and hypothyroidism presented with altered mental status for 8 months. He was previously diagnosed with myasthenia gravis, but therapy was discontinued due to infection. On presentation, he was wheelchair-bound with disorientation, proximal weakness, hyporeflexia and bradykinesia. MRI brain showed atrophy, and cerebrospinal fluid analysis revealed mildly elevated protein (58.8 mg/dL) without pleocytosis. Despite treatment for urinary tract infection and septic encephalopathy, his sensorium did not improve. A diagnosis of possible autoimmune encephalitis was considered, though antibody studies were negative. Whole-body Positron Emission Tomography - Computerized Tomography (PET-CT) ruled out malignancy and showed global hypokinesia, while echocardiography showed severe left ventricular systolic dysfunction. Positive acetylcholine receptor antibody led to intravenous immunoglobulin therapy, which improved his sensorium and cardiac dysfunction suggesting a positive association.

BMJ Case ReportsVol. 18(4)
Amrita Institute of Medical Sciences and Research Centre (IN)
Good health and well-being
Openalex Percentile: Top 87%
Autoimmune Neurological Disorders and Treatments
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