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对15例以肝功能异常为首发症状的系统性红斑狼疮患者的分析。

Analysis of 15 patients with abnormal liver function as the first systemic lupus erythematosus symptom.

作者信息

Gao Y, Li W, Meng Q-H, Liu H-X, Zhu Y-K

出版信息

Acta Gastroenterol Belg. 2016 Sep-Dec;79(2):441-446.

Abstract

OBJECTIVE

To understand the clinical characteristics of patients with abnormal liver function as the first symptom of systemic lupus erythematosus (SLE).

METHODS

Here, 15 patients admitted to a hospital from January 2010 to December 2013 with initial presentation of lupus-related hepatitis or cirrhosis were included. Their SLE-DAI scores and clinical and laboratory data were collected. All cases received liver protection therapy and active SLE controlling treatment with methylprednisolone combined with rapamycin.

RESULTS

When hepatic abnormalities were the most prominent feature during the first visit, the patient was more likely to receive an incorrect diagnosis or be diagnosed with SLE late. Of the 15 cases, only 7 (46.7%) were identified as SLE within a week of presentation of abnormal liver function ; meanwhile, the 7 remaining patients (46.7%) were not correctly diagnosed until more than 2 weeks later and as late as 4 months ; in addition, 1 patient was not diagnosed with SLE until 8 years after the initial presentation of abnormal liver function. In the 3-month follow-up after active treatment, liver function was completely restored in 10 cases with no cirrhosis and significantly improved in 3 patients who still had cirrhosis. Another case showed no improvement in liver function and was self-discharged, and another died from chronic liver failure.

CONCLUSION

Liver injury caused by SLE is not uncommon, and it is easy to tentatively diagnose it as hepatitis, delaying the correct diagnosis of SLE. In such patients, physicians should perform a thorough differential diagnosis as soon as possible and administer proper treatment. Corticosteroid conjugated with immunosuppressants with no or little liver toxicity would be suitable for patients with SLE-induced liver injury. (Acta gastroenterol. belg., 2016, 79, 441-446).

摘要

目的

了解以肝功能异常为首发症状的系统性红斑狼疮(SLE)患者的临床特征。

方法

纳入2010年1月至2013年12月在某医院收治的15例以狼疮相关肝炎或肝硬化为初始表现的患者。收集他们的SLE-DAI评分以及临床和实验室数据。所有病例均接受保肝治疗以及甲泼尼龙联合雷帕霉素的积极SLE控制治疗。

结果

当肝脏异常是首次就诊时最突出的特征时,患者更有可能被误诊或较晚被诊断为SLE。在这15例病例中,仅7例(46.7%)在肝功能异常出现后1周内被确诊为SLE;同时,其余7例患者(46.7%)直到2周多后甚至4个月才被正确诊断;此外,1例患者在肝功能异常首次出现8年后才被诊断为SLE。积极治疗后的3个月随访中,10例无肝硬化的患者肝功能完全恢复,3例仍有肝硬化的患者肝功能显著改善。另一例肝功能无改善且自动出院,还有1例死于慢性肝衰竭。

结论

SLE所致肝损伤并不少见,且容易被初步诊断为肝炎,从而延误SLE的正确诊断。对于此类患者,医生应尽快进行全面的鉴别诊断并给予恰当治疗。皮质类固醇联合肝毒性小或无肝毒性的免疫抑制剂适用于SLE所致肝损伤患者。(《比利时胃肠病学学报》,2016年,79卷,441 - 446页)

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