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系统性红斑狼疮中的急性横贯性脊髓病:临床表现、治疗及预后

Acute transverse myelopathy in systemic lupus erythematosus: clinical presentation, treatment, and outcome.

作者信息

Mok C C, Lau C S, Chan E Y, Wong R W

机构信息

Department of Medicine, Queen Mary Hospital, Pokfulam, Hong Kong, People's Republic of China.

出版信息

J Rheumatol. 1998 Mar;25(3):467-73.

PMID:9517765
Abstract

OBJECTIVE

Acute transverse myelopathy (ATM) is a rare manifestation of systemic lupus erythematosus (SLE). The pathogenesis is unclear and the optimal management strategy is uncertain because of the lack of controlled trials. In this study, the clinical presentation, autoantibody profile, treatment, and outcome of cases of ATM in our local SLE population were retrospectively analyzed and compared with SLE controls.

RESULTS

Ten cases of ATM were identified among 315 patients with SLE studied, giving a prevalence of 3.2%. In 5 of the patients, ATM was the initial manifestation of SLE. The cervical cord was the most common site of involvement (50%). Cerebrospinal fluid abnormalities were present in 63% of the patients, while magnetic resonance imaging (MRI) of the spinal cord revealed abnormal T2 signals in 56%. Only one patient had lupus nephritis. ATM was not associated with antiribosomal P or anti-extractable nuclear antigen (anti-ENA) antibodies. Positive dsDNA antibody was present in 40% of the ATM cases, which was significantly lower than that of patients with active SLE without spinal cord disease (75%; p = 0.04). No significant differences in the prevalence of anticardiolipin antibodies and lupus anticoagulant between the ATM and the non-ATM group were observed. Only 3 patients with ATM showed hypocomplementemia or disease activity in other organs at the time of diagnosis. All the patients with ATM received corticosteroids, while 9 were given cytotoxic agents in addition. The response to treatment was variable -- 40% of patients had complete motor and sphincter recovery and 30% had mild residual spasticity of the lower limbs.

CONCLUSION

In our SLE population, ATM was not associated with antiribosomal P, anti-ENA, or antiphospholipid antibodies. Systemic complement activation was not evident in most patients during the acute phase of myelitis. Early aggressive therapy using a combination of corticosteroid and cytotoxic agents is associated with a satisfactory outcome. Further prospective study is needed to delineate the best treatment and its efficacy in the prevention of relapses.

摘要

目的

急性横贯性脊髓炎(ATM)是系统性红斑狼疮(SLE)的一种罕见表现。其发病机制尚不清楚,且由于缺乏对照试验,最佳治疗策略也不明确。在本研究中,我们对本地SLE患者群体中ATM病例的临床表现、自身抗体谱、治疗及结局进行了回顾性分析,并与SLE对照进行比较。

结果

在研究的315例SLE患者中,确诊10例ATM,患病率为3.2%。其中5例患者,ATM是SLE的首发表现。颈髓是最常受累部位(50%)。63%的患者脑脊液异常,而脊髓磁共振成像(MRI)显示56%的患者T2信号异常。仅1例患者有狼疮性肾炎。ATM与抗核糖体P或抗可提取核抗原(抗ENA)抗体无关。40%的ATM病例双链DNA抗体阳性,显著低于无脊髓疾病的活动性SLE患者(75%;p = 0.04)。ATM组与非ATM组在心磷脂抗体和狼疮抗凝物患病率方面未观察到显著差异。仅3例ATM患者在诊断时出现低补体血症或其他器官的疾病活动。所有ATM患者均接受了皮质类固醇治疗,另外9例给予了细胞毒性药物。治疗反应不一——40%的患者运动和括约肌功能完全恢复,30%的患者下肢有轻度残余痉挛。

结论

在我们的SLE患者群体中,ATM与抗核糖体P、抗ENA或抗磷脂抗体无关。在脊髓炎急性期,大多数患者全身补体激活不明显。早期联合使用皮质类固醇和细胞毒性药物进行积极治疗与满意的结局相关。需要进一步的前瞻性研究来确定最佳治疗方法及其预防复发的疗效。

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