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Autoimmune Limbic Encephalitis

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Detalhes bibliográficos
Resumo:Limbic encephalitis is a rare but increasingly recognized disorder. The sudden onset of symptoms such as confusion, cognitive impairment, irritability, depression, hallucinations, is one of the main characteristics. It is an inflammatory disease involving the temporal lobes, which explains the frequency of seizures. We report the case of a 27-year-old man, presenting hyperosmolar syndrome (owing to new onset diabetes mellitus), acute confusional state and sudden onset of seizures. Several diagnostic hypotheses were raised: infectious meningoencephalitis, autoimmune encephalitis, and metabolic encephalopathy. Despite treatment (antibiotics, correction of hyperosmolar state and anticonvulsant therapy), continuous cognitive deterioration and seizures persisted. We raised the hypothesis of an autoimmune limbic encephalitis by anti-GAD antibodies and treated with human immunoglobulin. There was a dramatic improvement, corroborating the diagnosis (along with imaging findings). Although difficult to diagnose, limbic encephalitis should be considered when studying acute confusional states with psychiatric symptoms and seizures. Clinical suspicion and early treatment are essential for therapeutic success.
Autores principais:Barbosa, Cristiana
Outros Autores:Patrão, Luís; Bettencourt, Victor; Pereira, Sara; Domingues, Joana; Garrido, António
Assunto:Doenças Autoimunes Encefalite Límbica Autoimmune Diseases Limbic Encephalitis
Ano:2015
País:Portugal
Tipo de documento:artigo
Tipo de acesso:unknown
Instituição associada:Sociedade Portuguesa de Medicina Interna
Idioma:português
Origem:Revista Portuguesa de Medicina Interna
Descrição
Resumo:Limbic encephalitis is a rare but increasingly recognized disorder. The sudden onset of symptoms such as confusion, cognitive impairment, irritability, depression, hallucinations, is one of the main characteristics. It is an inflammatory disease involving the temporal lobes, which explains the frequency of seizures. We report the case of a 27-year-old man, presenting hyperosmolar syndrome (owing to new onset diabetes mellitus), acute confusional state and sudden onset of seizures. Several diagnostic hypotheses were raised: infectious meningoencephalitis, autoimmune encephalitis, and metabolic encephalopathy. Despite treatment (antibiotics, correction of hyperosmolar state and anticonvulsant therapy), continuous cognitive deterioration and seizures persisted. We raised the hypothesis of an autoimmune limbic encephalitis by anti-GAD antibodies and treated with human immunoglobulin. There was a dramatic improvement, corroborating the diagnosis (along with imaging findings). Although difficult to diagnose, limbic encephalitis should be considered when studying acute confusional states with psychiatric symptoms and seizures. Clinical suspicion and early treatment are essential for therapeutic success.