Coutinho J, Lima M, dos Anjos Teixeira M, Cabeda J M, Leite F, Justiça B
Service of Clinical Haematology, St. Antonio's Hospital, Porto, Portugal.
Acta Haematol. 1998;100(4):207-10. doi: 10.1159/000040906.
This case report details a single patient with pure red cell aplasia (PRCA) associated with clonal CD3+, TCRalphabeta+, TCR-Vbeta8+, CD8+, CD57+ large granular lymphocytosis whose anaemia did not respond to conventional immunosuppressive therapy but did respond to cyclosporin A (CsA). The patient has become dependent on CsA for 7 years in order to control anaemia due to associated PRCA.
本病例报告详细介绍了一名患有纯红细胞再生障碍性贫血(PRCA)并伴有克隆性CD3 +、TCRαβ +、TCR-Vβ8 +、CD8 +、CD57 +大颗粒淋巴细胞增多症的患者,其贫血对传统免疫抑制治疗无反应,但对环孢素A(CsA)有反应。为控制因相关PRCA导致的贫血,该患者已依赖CsA达7年。