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首页> 外文期刊>Clinical Rheumatology >Transverse myelitis, a rare neurological manifestation of mixed connective tissue disease—a case report and a review of literature
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Transverse myelitis, a rare neurological manifestation of mixed connective tissue disease—a case report and a review of literature

机译:横向脊髓炎,混合性结缔组织病的罕见神经系统表现—病例报告和文献复习

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摘要

Although neurological involvement occurs in about 10% of patients with mixed connective tissue disease (MCTD), acute transverse myelitis (TM) has only been described in seven cases of MCTD. We hereby report a case of 70-year-old white female with transverse myelitis complicating her underlying MCTD. Our patient presented with lower extremity weakness, loss of sensation and incontinence one year after her diagnosis of MCTD. Her work-up revealed an abnormal MRI, with findings consistent with TM. She had an excellent response to initial therapy with six cycles of monthly intravenous immunoglobulins and steroids, with subsequent maintenance on azathioprine. She had a good neurological recovery with mild residual sequelae only. On basis of this case report and review of literature, we recommend ongoing surveillance and reporting of this rare neurological presentation in MCTD.
机译:尽管约有10%的混合性结缔组织病(MCTD)患者发生神经系统受累,但仅在7例MCTD中描述了急性横贯性脊髓炎(TM)。我们在此报告一例70岁的白人女性,患有横纹肌炎,使其基础的MCTD复杂化。诊断MCTD一年后,该患者出现下肢无力,感觉丧失和大小便失禁。她的检查发现MRI异常,发现与TM一致。她对最初的治疗有很好的反应,每月静脉注射免疫球蛋白和类固醇六个周期,随后维持硫唑嘌呤。她的神经恢复良好,仅残留轻度后遗症。根据此病例报告和文献综述,我们建议对MCTD中这种罕见的神经系统表现进行持续的监测和报告。

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