ArticleCureus2025
Hashimoto's Encephalopathy: A Rare Clinical Diagnosis in a Male Pediatric Patient.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
3 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Hashimoto's encephalopathy (HE) is very uncommon in the pediatric literature. It is most often characterized by altered mental status (AMS) that can range from mild confusion to hallucinations and severe agitation. The exact pathophysiologic mechanism of HE is unclear. The most popular proposed mechanism describes an immune-mediated process as opposed to a direct effect of thyroid hormone or thyroid antibodies on the central nervous system (CNS) despite the association in the name with Hashimoto's thyroiditis. Suspicion for HE is raised when a patient has encephalopathy, the presence of thyroid antibodies, and responsiveness to high-dose corticosteroids.
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