Camba L, Joyner M V
J Clin Pathol. 1985 Mar;38(3):297-300. doi: 10.1136/jcp.38.3.297.
We report a case of non-sideroblastic refractory anaemia which evolved to a double lymphomyeloproliferative disorder. At presentation, bone marrow appearances and peripheral blood pancytopenia without myelomonocytosis were consistent with a diagnosis of non-sideroblastic refractory anaemia. Subsequently, the patient developed pronounced myelomonocytosis and lymphocytosis with prolymphocytes. Light and transmission electron microscopy as well as surface marker studies were compatible with a diagnosis of prolymphocytic transformation of chronic lymphocytic leukaemia/prolymphocytic leukaemia associated with myelomonocytic leukaemia. The pathogenesis of such double lympho-myeloproliferative disorders is discussed in the light of the evidence for common lymphoid and myeloid progenitor cells and some recent advances in the immunology of the myelodysplastic syndromes.
我们报告一例非铁粒幼细胞性难治性贫血,该病例进展为双淋巴骨髓增殖性疾病。初诊时,骨髓表现及外周血全血细胞减少且无骨髓单核细胞增多,符合非铁粒幼细胞性难治性贫血的诊断。随后,患者出现明显的骨髓单核细胞增多及淋巴细胞增多,并伴有幼淋巴细胞。光镜和透射电镜检查以及表面标志物研究结果符合慢性淋巴细胞白血病/幼淋巴细胞白血病向幼淋巴细胞转化并伴有骨髓单核细胞白血病的诊断。本文根据共同淋巴样和髓样祖细胞的证据以及骨髓增生异常综合征免疫学方面的一些最新进展,对这种双淋巴骨髓增殖性疾病的发病机制进行了讨论。