Wernicke Encephalopathy in Anorexia Nervosa

Date of submission: 27-09-2018 | Date of acceptance: 02-10-2019 | Published: 02-04-2020

Authors

  • Carla Alves Pereira Psychiatric Department, Tondela/Viseu Hospital Center, Viseu, Portugal
  • Carina Ferreira Pediatrics Department, Tondela/Viseu Hospital Center, Viseu, Portugal
  • Diana Brigadeiro Psychiatric Department, Sousa Martins Hospital, Guarda, Portugal
  • Elisabete Santos Pediatrics Department, Tondela/Viseu Hospital Center, Viseu, Portugal
  • Tânia Casanova Psychiatric Department, Tondela/Viseu Hospital Center, Viseu, Portugal
  • Paulo Santos Psychiatric Department, Tondela/Viseu Hospital Center, Viseu, Portugal

DOI:

https://doi.org/10.25754/pjp.2020.15049

Abstract

Wernicke’s encephalopathy is an acute neuropsychiatric syndrome resulting from thiamine deficiency (vitamin B1) associated with significant morbidity and mortality. It has classically been described by the triad of mental status changes, ophthalmoplegia, and ataxia. However, its presentation can vary and there is relatively non-specific and oftentimes poorly recognized clinical presentation of Wernicke Encephalopathy. It has traditionally been associated with alcoholism but it may also occur in patients with subacute or chronic conditions that increase metabolic demand or cause significant malnutrition. In this review, the authors propose to describe a clinical case of Wernicke's Encephalopathy in a 13-year-old girl with anorexia nervosa - restrictive type, emphasizing the various aspects underlying these entities. The diagnosis of Wernicke's Encephalopathy should be considered in anorexia nervosa whenever there is an mental status change, although the symptoms of the classic triad are not present.

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Published

2020-04-16

Issue

Section

Case reports

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