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1例化疗改善的副肿瘤性缓解血清阴性对称性滑膜炎伴凹陷性水肿综合征病例

A Case of Paraneoplastic Remitting Seronegative Symmetrical Synovitis with Pitting Edema Syndrome Improved by Chemotherapy.

作者信息

Sakamoto Takahiko, Ota Shuji, Haruyama Terunobu, Ishihara Masashi, Natsume Maika, Fukasawa Yoko, Tanzawa Shigeru, Usui Ryo, Honda Takeshi, Ichikawa Yasuko, Watanabe Kiyotaka, Seki Nobuhiko

机构信息

Division of Medical Oncology, Department of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan.

出版信息

Case Rep Oncol. 2017 Dec 20;10(3):1131-1137. doi: 10.1159/000484977. eCollection 2017 Sep-Dec.

Abstract

The patient was a 69-year-old male who had started experiencing acute-onset pain in both shoulder joints and edema of both hands and feet. His symptoms progressively worsened within 1 month. Laboratory data indicated elevated CRP and erythrocyte sedimentation rate despite the normal range of antinuclear antibodies and rheumatoid factor and normal organ function. Furthermore, imaging data of the hand indicated synovitis without bone erosions. Meanwhile, chest CT revealed a lung tumor, leading to a diagnosis of primary lung adenocarcinoma with EGFR mutation (cT2aN3M0, stage IIIB). Based on these findings, he was diagnosed as suffering from paraneoplastic remitting seronegative symmetrical synovitis with pitting edema (RS3PE) syndrome. Thereafter, his symptoms disappeared as the tumor size was rapidly decreased by gefitinib therapy for lung adenocarcinoma. Currently, RS3PE syndrome can be classified as a vascular endothelial growth factor (VEGF)-associated disorder. Given that his symptoms improved by chemotherapy, the present case further supported the possible hypothesis that paraneoplastic RS3PE syndrome might be caused by tumor-induced VEGF. Therefore, the present case suggested that the symptoms of acute-onset joint pain accompanied by pitting edema in elderly patients should be considered suspicious for a malignant tumor, thereby warranting a detailed full-body examination.

摘要

该患者为69岁男性,开始出现双肩急性疼痛以及双手和双脚水肿。其症状在1个月内逐渐加重。实验室数据显示,尽管抗核抗体和类风湿因子在正常范围内且器官功能正常,但C反应蛋白和红细胞沉降率升高。此外,手部影像学数据显示滑膜炎但无骨质侵蚀。同时,胸部CT显示肺部有肿瘤,诊断为原发性肺腺癌伴表皮生长因子受体(EGFR)突变(cT2aN3M0,IIIB期)。基于这些发现,他被诊断为患有副肿瘤性缓解血清阴性对称性滑膜炎伴凹陷性水肿(RS3PE)综合征。此后,由于吉非替尼治疗肺腺癌使肿瘤大小迅速减小,他的症状消失。目前,RS3PE综合征可归类为血管内皮生长因子(VEGF)相关疾病。鉴于他的症状通过化疗得到改善,本病例进一步支持了副肿瘤性RS3PE综合征可能由肿瘤诱导的VEGF引起的假说。因此,本病例表明,老年患者急性发作的关节疼痛伴凹陷性水肿症状应怀疑为恶性肿瘤,从而需要进行详细的全身检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97c8/5803715/36e3dfd4a787/cro-0010-1131-g01.jpg

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