Chmiel J F, Wessel H U, Targoff I N, Pachman L M
Department of Pediatrics, Northwestern University Medical School, Chicago, IL, USA.
J Rheumatol. 1995 Apr;22(4):762-5.
This is the first report of a child with anti-Jo-1 antibody. At 10, she had a chronic cough, wheezing, dyspnea on exertion, a combined obstructive and restrictive ventilatory defect, and a decreased diffusion capacity compatible with alveolar fibrosis (lung biopsy). By age 12, she developed arthralgias, malar rash, frontal alopecia, Raynaud's phenomenon, and was seropositive for antinuclear antibodies, (SSA)Ro, Jo-1 and rheumatoid factor. At 16, symptomatic inflammatory myositis (elevated creatinine kinase, muscle biopsy) was documented with persistent anti-Jo-1. Her pulmonary symptoms have progressed despite appropriate therapy. Although her digits have become sausage shaped with swan neck deformities, joint pain is not frequent.
这是首例关于一名患有抗Jo-1抗体的儿童的报告。10岁时,她出现慢性咳嗽、喘息、活动时呼吸困难,存在阻塞性和限制性通气功能障碍合并症,以及与肺泡纤维化相符的弥散功能降低(肺活检)。到12岁时,她出现关节痛、颧部皮疹、额部脱发、雷诺现象,抗核抗体、(SSA)Ro、Jo-1和类风湿因子血清学检查呈阳性。16岁时,有症状性炎性肌炎(肌酸激酶升高,肌肉活检)被记录,且抗Jo-1持续存在。尽管进行了适当治疗,她的肺部症状仍在进展。虽然她的手指已呈腊肠样并伴有天鹅颈畸形,但关节疼痛并不频繁。