A Rare Case of Neuromyelitis Optica Spectrum Disorder Secondary to Primary Sjögren's Syndrome in an Older Woman.

Q4 Biochemistry, Genetics and Molecular Biology Prague medical report Pub Date : 2024-01-01 DOI:10.14712/23362936.2024.21
Hasan Huseyin Zorlu, Suleyman Emre Kocyigit
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引用次数: 0

Abstract

Primary Sjögren's syndrome is an autoimmune disorder that is characterized by lymphocytic infiltration of salivary and lacrimal glands. The extra-glandular manifestations might be arthritis, myalgia, glomerulonephritis, skin rashes, and neurologic involvement. One of the uncommon neurologic manifestations is neuromyelitis optica spectrum disorder (NMOSD). In the present case, an older woman is reported that was diagnosed with NMOSD secondary to keratoconjunctivitis sicca, which is rare in geriatric practice.

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一名老年妇女继发于原发性斯约格伦综合征的神经脊髓炎谱系障碍罕见病例。
原发性斯约格伦综合征是一种以唾液腺和泪腺淋巴细胞浸润为特征的自身免疫性疾病。腺外表现可能是关节炎、肌痛、肾小球肾炎、皮疹和神经系统受累。神经脊髓炎视神经谱系障碍(NMOSD)是其中一种不常见的神经系统表现。在本病例中,一名老年妇女被诊断为继发于角膜结膜炎的神经脊髓炎视网膜频谱障碍(NMOSD),这在老年医学中十分罕见。
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来源期刊
Prague medical report
Prague medical report Medicine-Medicine (all)
CiteScore
1.10
自引率
0.00%
发文量
19
审稿时长
20 weeks
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