Stanworth S J, Green L, Pumphrey R S, Swinson D R, Bhavnani M
Department of Immunology, St Mary's Hospital, Manchester.
J Clin Pathol. 1996 Apr;49(4):351-3. doi: 10.1136/jcp.49.4.351.
Felty syndrome, comprised of neutropenia, rheumatoid arthritis and splenomegaly, occurs in approximately 1% of patients with rheumatoid arthritis. Up to one third of these patients have an increased number of large granular lymphocytes. The usual immunophenotype of these cells is CD3+, CD8+, CD57+, T cell receptor (TCR) alpha beta. A patient with Felty syndrome and large granular lymphocytosis, who had an unusual immunophenotype CD3+, CD4-, CD8-, TCR gamma delta, is described. Her neutropenia responded to treatment with granulocyte colony stimulating factor (G-CSF), which was given in order to raise her neutrophil count prior to bilateral knee replacement surgery. Thus, Felty syndrome with large granular lymphocytosis is a heterogeneous condition, one in which TCR gamma delta large granular lymphocytosis may be found, and also shows a response to treatment with G-CSF.
费尔蒂综合征由中性粒细胞减少、类风湿性关节炎和脾肿大组成,约1%的类风湿性关节炎患者会出现该综合征。这些患者中多达三分之一的人外周血大颗粒淋巴细胞数量增加。这些细胞通常的免疫表型是CD3+、CD8+、CD57+、T细胞受体(TCR)αβ。本文描述了一名患有费尔蒂综合征和大颗粒淋巴细胞增多症的患者,其具有不寻常的免疫表型CD3+、CD4-、CD8-、TCRγδ。她的中性粒细胞减少症对粒细胞集落刺激因子(G-CSF)治疗有反应,在双侧膝关节置换手术前给予G-CSF是为了提高她的中性粒细胞计数。因此,伴有大颗粒淋巴细胞增多症的费尔蒂综合征是一种异质性疾病,其中可能会发现TCRγδ大颗粒淋巴细胞增多症,并且对G-CSF治疗也有反应。