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A Rare Case of Suspected Neuronal Intranuclear Inclusion Disease Requiring Differentiation From Neuro-Behçet’s Disease

A 69-year-old male patient with a long-standing history of Behçet’s disease was admitted to another hospital with minor physical injuries after a traffic accident. However, the patient was subsequently transferred to our facility because of a prolonged disorder of consciousness suspected to be relat...

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Detalles Bibliográficos
Autores principales: Sugisaki, Kota, Asakawa, Yohei, Kobayashi, Keiko, Ito, Mikako, Hori, Masao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082561/
https://www.ncbi.nlm.nih.gov/pubmed/37038582
http://dx.doi.org/10.7759/cureus.35928
Descripción
Sumario:A 69-year-old male patient with a long-standing history of Behçet’s disease was admitted to another hospital with minor physical injuries after a traffic accident. However, the patient was subsequently transferred to our facility because of a prolonged disorder of consciousness suspected to be related to neuro-Behçet’s disease (NBD). A thorough patient evaluation for determining the most appropriate treatment course led to a strong suspicion of neuronal intranuclear inclusion disease and predominantly ruled out NBD. This eliminated the need for unnecessary immunosuppressive intervention. Thereafter, the patient was transferred to a long-term care facility. This case highlights the importance of careful identification of pathological conditions before developing a treatment plan, regardless of the presence or absence of an underlying disease.