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[病例报告:类风湿关节炎与大颗粒淋巴细胞综合征]

[Case report: rheumatoid arthritis and large granular lymphocytes syndrome].

作者信息

Ingegnoli F, Arreghini M, Panni B, Capra R, Galbiati F, Bonara P, Marchesoni A

机构信息

Istituto Ortopedico Gaetano Pini, Milano, Italia.

出版信息

Reumatismo. 2002 Oct-Dec;54(4):357-60. doi: 10.4081/reumatismo.2002.357.

Abstract

Felty's syndrome (FS) is a rare complication (less than 1%) of rheumatoid arthritis (RA), with the clinical feature of splenomegaly and neutropenia. Approximately 10-40% of FS patients have an expansion of peripheral blood large granular lymphocytes (LGL). This cell population mainly consists of two subsets: cytotoxic T cells (CD8+, CD57+) and natural killer cells (CD3-,CD8-,CD56+). It has been hypothesised that LGL expansion could be responsible for neutropenia by suppressing neutrophil precursors in the bone marrow, but various mechanisms have been proposed to explain this association. We report a case of a 60-year-old woman with rheumatoid factor positive RA who developed LGL expansion responsible for splenomegaly, but without neutropenia. In conclusion, LGL expansion is an uncommon complication of RA and may be responsible for both FS and clinical pictures resembling FS.

摘要

费尔蒂综合征(FS)是类风湿关节炎(RA)的一种罕见并发症(少于1%),其临床特征为脾肿大和中性粒细胞减少。约10% - 40%的FS患者外周血大颗粒淋巴细胞(LGL)增多。该细胞群主要由两个亚群组成:细胞毒性T细胞(CD8 +、CD57 +)和自然杀伤细胞(CD3 -、CD8 -、CD56 +)。据推测,LGL增多可能通过抑制骨髓中的中性粒细胞前体导致中性粒细胞减少,但也提出了各种机制来解释这种关联。我们报告一例60岁类风湿因子阳性的RA女性患者,其出现了导致脾肿大的LGL增多,但无中性粒细胞减少。总之,LGL增多是RA的一种罕见并发症,可能导致FS以及类似FS的临床表现。

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