Tesar J T, McMillan V, Molina R, Armstrong J
Department of Medicine, Walter Reed Army Medical Center, Washington, D.C. 20307-5001.
Am J Med. 1992 Jun;92(6):686-92. doi: 10.1016/0002-9343(92)90788-d.
Three cases of optic neuropathy associated with primary Sjögren's syndrome are reported. All three patients had clinical manifestations of primary Sjögren's syndrome, although two of the patients did not report sicca symptoms at initial examination. Two patients had focal neurologic signs in addition to optic neuropathy. The differentiation of this syndrome of optic neuropathy, focal neurologic signs, and Sjögren's syndrome from multiple sclerosis and antiphospholipid antibody syndrome is important for reasons of treatment and prognosis. This diagnostic differentiation was facilitated by positive tests for xerophthalmia and findings of positive minor salivary gland biopsy. High titers of antinuclear antibody, anti-SSA(Ro), and anti-SSB(La), and the absence of antiphospholipid antibodies provided additional help in the differential diagnosis. In 5 years of observation, none of the patients developed symptoms of multiple sclerosis or additional connective tissue disorders.
报告了3例与原发性干燥综合征相关的视神经病变。所有3例患者均有原发性干燥综合征的临床表现,尽管其中2例患者在初次检查时未报告干眼症状。除视神经病变外,2例患者还有局灶性神经体征。由于治疗和预后的原因,将这种伴有视神经病变、局灶性神经体征和干燥综合征的综合征与多发性硬化症和抗磷脂抗体综合征相鉴别很重要。干眼症检测阳性以及小唾液腺活检结果阳性有助于这种诊断鉴别。高滴度的抗核抗体、抗SSA(Ro)和抗SSB(La),以及抗磷脂抗体的缺乏为鉴别诊断提供了额外帮助。在5年的观察期内,没有患者出现多发性硬化症症状或其他结缔组织疾病。