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首页> 外文期刊>Joint, bone, spine : >Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) and oligoarthritis.
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Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) and oligoarthritis.

机译:窦组织细胞增生症伴大量淋巴结病(罗赛-多夫曼病)和寡关节炎。

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摘要

A 24-year-old woman who had sinus histiocytosis with massive lymphadenopathy (SHML, Rosai-Dorfman disease) also had oligoarthritis. We found only four previously reported cases of SHML with clinical joint disease. The clinical picture may suggest rheumatoid arthritis or a spondylarthropathy with peripheral joint involvement. SHML should be considered routinely among the differential diagnoses in young patients with arthritis and large lymphadenopathies. There is no consensus regarding the treatment. In our patient, conventional disease-modifying antirheumatic drugs followed by 3 months of adalimumab then 3 months of etanercept had no effect on the symptoms.
机译:一名患有窦性组织细胞增生症并伴有严重淋巴结病(SHML,罗萨-多夫曼病)的24岁女性也患有寡关节炎。我们仅发现四例先前报道的临床关节疾病SHML病例。临床表现可能提示类风湿性关节炎或脊椎关节病伴有周围关节受累。在患有关节炎和大淋巴腺病的年轻患者的鉴别诊断中,应常规考虑SHML。关于治疗尚无共识。在我们的患者中,常规的改变疾病的抗风湿药,接着是3个月的阿达木单抗,然后是3个月的依那西普对症状没有影响。

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