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疑似系统性红斑狼疮患者的丘疹结节性黏蛋白沉积症

Papulonodular mucinosis in a suspected systemic lupus erythematosus patient.

作者信息

Ausavarungnirun Rujikan, Srisuttiyakorn Chutika

出版信息

J Med Assoc Thai. 2014 Feb;97 Suppl 2:S239-42.

PMID:25518200
Abstract

We present a 45-years-old suspected systemic lupus erythematosus (SLE) woman who had papulonodular mucinosis (PNM), without other cutaneous LE lesion. The lesions of PNM distributed on both legs which were an unusual location. In addition, the renal involvement was found and suspected from lupus nephritis. The patient was treated with prednisolone, mycofenolate mofetil and chloroquine. After 2 months of follow-up, the renal involvement was improved along with the disappearance ofskin lesions.

摘要

我们报告一位45岁疑似系统性红斑狼疮(SLE)的女性患者,她患有丘疹结节性粘蛋白病(PNM),无其他皮肤性红斑狼疮病变。PNM的皮损分布于双下肢,这是一个不寻常的部位。此外,发现有肾脏受累,并怀疑为狼疮性肾炎。该患者接受了泼尼松龙、霉酚酸酯和氯喹治疗。经过2个月的随访,肾脏受累情况有所改善,同时皮肤病变消失。

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