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伴有凹陷性水肿的缓解型血清阴性对称性滑膜炎:12例研究

Remitting seronegative symmetrical synovitis with pitting oedema: a study of 12 cases.

作者信息

Paira S, Graf C, Roverano S, Rossini J

机构信息

Hospital José M Cullen, Santa Fe, Argentina.

出版信息

Clin Rheumatol. 2002 May;21(2):146-9. doi: 10.1007/pl00011218.

DOI:10.1007/pl00011218
PMID:12086166
Abstract

Twelve patients with remitting seronegative symmetrical synovitis with pitting oedema (RS3PE) were analysed. Eight of them had typical RS3PE without underlying disease, and four presented associated neoplasia. The first patients experienced an excellent response to low doses of prednisone, and they all achieved complete and permanent remission. The mean treatment duration was 18 months and the mean follow-up was 4.4 years. During the follow-up, none of these patients relapsed, had fever or general health deterioration, and hand and foot radiographs did not show erosion. One of them developed a panarteritis nodosa 6 years later. Four RS3PE patients had associated neoplasia. Two were with solid malignancies, and the other two presented haematological malignancies. In one of them RS3PE preceded the diagnosis of malignancy. The diagnosis of RS3PE in the other patients was subsequent to cancer. The first patients presented clinical characteristics suggestive of paraneoplastic RS3PE, and they had a poor response to corticosteroid therapy. Two patients died, and the rest of them had a complete response to surgical resection of the tumour or to chemotherapy. In general, idiopathic RS3PE patients do not show either general health deterioration or fever and they do respond to low doses of steroids (10 mg/day). We observed strong contrasts with the results obtained when treating RS3PE patients with associated neoplasia. In patients with RS3PE the presence of systemic symptoms along with resistance to low doses of corticosteroid therapy should alert the physician to the possible presence of malignancy.

摘要

对12例伴有凹陷性水肿的缓解型血清阴性对称性滑膜炎(RS3PE)患者进行了分析。其中8例患有典型的无潜在疾病的RS3PE,4例伴有相关肿瘤。首例患者对低剂量泼尼松反应良好,所有患者均实现完全且永久缓解。平均治疗时长为18个月,平均随访时间为4.4年。随访期间,这些患者均未复发、发热或出现全身健康状况恶化,手足X线片未显示侵蚀。其中1例6年后发生结节性多动脉炎。4例RS3PE患者伴有相关肿瘤。2例为实体恶性肿瘤,另外2例为血液系统恶性肿瘤。其中1例RS3PE先于恶性肿瘤诊断出现。其他患者的RS3PE诊断在癌症之后。首例患者表现出提示副肿瘤性RS3PE的临床特征,对皮质类固醇治疗反应不佳。2例患者死亡,其余患者对肿瘤手术切除或化疗完全缓解。一般来说,特发性RS3PE患者不会出现全身健康状况恶化或发热,且对低剂量类固醇(10毫克/天)有反应。我们观察到,在治疗伴有相关肿瘤的RS3PE患者时,结果存在强烈反差。在RS3PE患者中,出现全身症状以及对低剂量皮质类固醇治疗耐药应提醒医生警惕可能存在恶性肿瘤。

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