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[费尔蒂综合征的机制及长期病程]

[Mechanism of Felty's syndrome and long-term course].

作者信息

Feldmann J L, Menkès C J

机构信息

Service de Rhumatologie et de Réadaptation Fonctionnelle, Centre Hospitalier, Argenteuil.

出版信息

Rev Rhum Mal Osteoartic. 1988 Mar 15;55(4):255-9.

PMID:3375772
Abstract

The authors report 18 cases of Felty's syndrome followed, in an average, for 5 years (1 to 12 years). There were 3 deaths, 9 patients are in complete remission, 6 others still show signs of the disease: splenomegaly (4 cases), leucopenia (1 case) and only one complete Felty's syndrome. Steroid therapy has proved to be effective regardless of the mechanism of the neutropenia specified in 9 cases by an isotopic study. Prognosis and infectious risk are difficult to determine but the overall course was rather favorable.

摘要

作者报告了18例费尔蒂综合征患者,平均随访5年(1至12年)。有3例死亡,9例患者完全缓解,另外6例仍有疾病迹象:脾肿大(4例)、白细胞减少(1例),仅1例为典型费尔蒂综合征。同位素研究表明,无论9例中性粒细胞减少的机制如何,类固醇治疗已证明有效。预后和感染风险难以确定,但总体病程较为有利。

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