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嗜酸性筋膜炎:52例患者的临床谱及治疗反应

Eosinophilic fasciitis: clinical spectrum and therapeutic response in 52 cases.

作者信息

Lakhanpal S, Ginsburg W W, Michet C J, Doyle J A, Moore S B

机构信息

Mayo Clinic/Mayo Foundation, Rochester, MN 55905.

出版信息

Semin Arthritis Rheum. 1988 May;17(4):221-31. doi: 10.1016/0049-0172(88)90008-x.

Abstract

The clinical course of 52 cases with eosinophilic fasciitis observed at the Mayo Clinic has been described. Cutaneous changes included pitting edema, peau d'orange, and induration, and may affect virtually any body surface area. In addition, localized morphea was present in 15 cases. Arthritis was observed in 21 patients; 29 patients had flexion contractures and 12 had carpal tunnel syndrome. Associated hematologic diseases were found in five patients; thrombocytopenia in two, myeloproliferative disorder in one, myelomonocytic leukemia in one, and chronic lymphocytic leukemia in one. Peripheral blood eosinophilia was noted in 33 of 52 patients, hypergammaglobulinemia was noted in 17 of 49, and elevated sedimentation rate was noted in 15 of 52. Nonspecific EMG changes were seen in 11 of 15 patients. None had clinical involvement of the kidneys, lungs, or heart. No significant association between any HLA-A, -B, or -DR and eosinophilic fasciitis was seen. Prednisone and hydroxychloroquine seemed equally beneficial in treatment; however, some cases showed spontaneous recovery, making evaluation of therapeutic efficacy difficult. Relapses occurred in some cases.

摘要

梅奥诊所观察到的52例嗜酸性筋膜炎患者的临床病程已被描述。皮肤改变包括凹陷性水肿、橘皮样皮肤和硬结,几乎可累及身体任何体表区域。此外,15例患者存在局限性硬斑病。21例患者出现关节炎;29例患者有屈曲挛缩,12例有腕管综合征。5例患者发现相关血液系统疾病;2例血小板减少,1例骨髓增殖性疾病,1例骨髓单核细胞白血病,1例慢性淋巴细胞白血病。52例患者中有33例外周血嗜酸性粒细胞增多,49例中有17例高球蛋白血症,52例中有15例血沉升高。15例患者中有11例出现非特异性肌电图改变。无一例患者出现肾脏、肺部或心脏的临床受累。未发现任何HLA - A、- B或 - DR与嗜酸性筋膜炎之间存在显著关联。泼尼松和羟氯喹在治疗中似乎同样有效;然而,一些病例显示自发恢复,使得治疗效果评估困难。部分病例出现复发。

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