Neuropsychiatric manifestations in systemic lupus erythematosus and Sjogren's disease.

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Tác giả: Simone Appenzeller, Amanda Carolina Miranda Costa, Bruna Martins De Aquino, Samuel de Oliveira Andrade, Jean Marcos De Souza, Nunes Dpf, Marcondes Cavalcante França, Paulo Rogério Júlio, Rodrigo Marchi-Silva, Alberto Rolim Muro Martinez, Tais Nitsch Mazzola, Timothy B Niewold, Danilo Rodrigues Pereira, Fabiano Reis, Zahi Touma

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: Netherlands : Autoimmunity reviews , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 90802

INTRODUCTION: Autoimmune diseases often present in a systemic manner, affecting various organs and tissues. Involvement of the central and peripheral nervous system is not uncommon in these conditions and is associated with high morbidity and mortality. Therefore, early recognition of the neuropsychiatric manifestations associated with rheumatologic diseases is essential for the introduction of appropriate therapies with the objective of providing a better quality of life for individuals. OBJECTIVE: To provide a literature review of the neuropsychiatric manifestations related to Systemic Lupus Erythematosus (SLE) and primary Sjögren's Disease (pSD), through the description of signs, symptoms, and immunological variables associated with these conditions. METHODS: A literature review was conducted by searching for national and international articles available in the SciELO and PubMed databases related to the description of neurological and psychiatric manifestations in patients with the rheumatologic diseases of interest in this study. RESULTS: The main NP manifestations presented in SLE and pSD are discussed, focusing on clinical presentation and etiology. Treatment option are, however, mainly based on expert opinion, since a few randomized controlled trials have been done. CONCLUSIONS: There is a high prevalence of neuropsychiatric manifestations associated with SLE and pSD. The variety of physiopathology pathways may explain the variety of symptoms, however pathological findings are rare. Multicenter studies on attribution protocols and treatment are necessary to address the current gaps.
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