Refractory pure red cell aplasia associated with T-cell large granular lymphocyte leukemia treated by ruxolitinib.
Yuemin GongYue LiXiaoyu ChenHui YangYawen ZhangGuang-Sheng HeLei FanPublished in: Annals of hematology (2024)
Acquired pure red cell aplasia (PRCA) is a rare syndrome characterized by normocytic normochromic anemia with severe reticulocytopenia and absence of erythroid precursors in the bone marrow. For refractory PRCA patients, the low response rate and high toxicity of alternative therapies pose a great challenge. T-cell large granular lymphocyte (T-LGL) leukemia is one of the most common conditions in secondary PRCA and also the most difficult form to manage with an inferior treatment response to other secondary PRCA forms. T-LGL leukemia exhibits sustained activation of the intracellular JAK-STAT signaling pathway. We herein report a case of PRCA associated with T-LGL leukemia that had been refractory to multiple lines of therapies and was successfully treated by ruxolitinib. The patient achieved complete remission and tolerated ruxolitinib well without occurrence of neutropenia or thrombocytopenia. This preliminary finding favors ruxolitinib as a potential salvage therapy for refractory PRCA associated with T-LGL leukemia.
Keyphrases
- bone marrow
- acute myeloid leukemia
- signaling pathway
- single cell
- end stage renal disease
- mesenchymal stem cells
- chronic kidney disease
- newly diagnosed
- ejection fraction
- case report
- epithelial mesenchymal transition
- risk assessment
- peripheral blood
- prognostic factors
- early onset
- systemic lupus erythematosus
- peritoneal dialysis
- combination therapy
- human health
- iron deficiency