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抗MDA5抗体阳性临床无肌病性皮肌炎长期缓解后复发:一例报告

Recurrence of anti-MDA5 antibody-positive clinically amyopathic dermatomyositis after long-term remission: A case report.

作者信息

Endo Yushiro, Koga Tomohiro, Ishida Midori, Fujita Yuya, Tsuji Sosuke, Takatani Ayuko, Shimizu Toshimasa, Sumiyoshi Remi, Igawa Takashi, Umeda Masataka, Fukui Shoichi, Nishino Ayako, Kawashiri Shin-Ya, Iwamoto Naoki, Ichinose Kunihiro, Tamai Mami, Nakamura Hideki, Origuchi Tomoki, Kuwana Masataka, Hosono Yuji, Mimori Tsuneyo, Kawakami Atsushi

机构信息

Department of Rheumatology, Unit of Advanced Preventive Medical Sciences, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

出版信息

Medicine (Baltimore). 2018 Jun;97(26):e11024. doi: 10.1097/MD.0000000000011024.

Abstract

RATIONALE

Among all dermatomyositis (DM) patients, antimelanoma differentiation-associated gene 5 antibody (anti-MDA5 Ab) positive patients have significantly poor short-term mortality, whereas they experience less relapses over the long term after the remission. We report the case of a patient with anti-MDA5 Ab-positive clinically amyopathic dermatomyositis (CADM) with the recurrence of interstitial lung disease (ILD) after 7 years of remission. There has been no case report of an anti-MDA5 Ab-positive DM patient with the recurrence of ILD after 7 years of long-term remission.

PATIENT CONCERNS

A 70-year-old Japanese woman was diagnosed with anti-MDA5 Ab-positive CADM and ILD. After achieving 7 years long-term remission, she was admitted to our department with erythema on the fingers and interstitial pneumonia. Her anti-MDA5 Ab titer was elevated.

DIAGNOSES

We diagnosed recurrent CADM complicated with ILD.

INTERVENTIONS

We successfully treated her with 1,000 mg of methyl-prednisolone pulse and intravenous cyclophosphamide therapy followed by prednisolone 50 mg/day and an increase of cyclosporine.

OUTCOMES

After that treatment, the patient's skin symptoms and interstitial pneumonia were relieved. All laboratory investigations such as ferritin, the serum markers of interstitial pneumonia (i.e., SP-A, SP-D), and the titer of anti-MDA5 Ab showed signs of improvement.

LESSONS

Her case suggests that careful physical examinations and monitoring the serum markers are important even after long-term remission is achieved.

摘要

原理

在所有皮肌炎(DM)患者中,抗黑色素瘤分化相关基因5抗体(抗MDA5抗体)阳性患者的短期死亡率显著较高,而在缓解后长期复发较少。我们报告一例抗MDA5抗体阳性的临床无肌病性皮肌炎(CADM)患者,在缓解7年后出现间质性肺病(ILD)复发。此前尚无抗MDA5抗体阳性的DM患者在长期缓解7年后出现ILD复发的病例报告。

患者情况

一名70岁日本女性被诊断为抗MDA5抗体阳性的CADM和ILD。在实现7年长期缓解后,她因手指红斑和间质性肺炎入住我科。其抗MDA5抗体滴度升高。

诊断

我们诊断为复发性CADM合并ILD。

干预措施

我们成功地用1000mg甲泼尼龙冲击治疗及静脉注射环磷酰胺,随后给予泼尼松龙50mg/天并增加环孢素进行治疗。

结果

经过该治疗后,患者的皮肤症状和间质性肺炎得到缓解。所有实验室检查,如铁蛋白、间质性肺炎血清标志物(即SP-A、SP-D)以及抗MDA5抗体滴度均显示改善迹象。

经验教训

她的病例表明,即使在实现长期缓解后,仔细的体格检查和监测血清标志物也很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1154/6039648/cf70a02da925/medi-97-e11024-g001.jpg

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