Abbrederis K, Stühlinger W
Acta Med Austriaca. 1981;8(4):128-30.
Among 17 patients with non acute monocytic (CMoL) and myelomonocytic leukemia (CMML) one patient presented with atypical findings and an unusual clinical course. Prominent massive pancytopenia had occurred ever since the diagnosis was established. To our knowledge this symptom has not been described in cases with CMML and CMoL. Splenectomy afforded temporary improvement of the anemia but induced sustained, marked thrombocytosis. An unusually prolonged survival time of 44 months was achieved, presumably by the continuous, careful replacement of blood, the splenectomy and the relinquishment of cytotoxic therapy. A gradual, continuously developing blastic crisis and finally the transition to an acute leukemia were observed.
在17例非急性单核细胞白血病(CMoL)和骨髓单核细胞白血病(CMML)患者中,有1例表现出非典型特征和不寻常的临床病程。自确诊以来,一直存在显著的全血细胞减少。据我们所知,这种症状在CMML和CMoL病例中尚未见报道。脾切除术后贫血得到了暂时改善,但引发了持续的、明显的血小板增多症。患者存活了44个月,时间异常延长,这可能得益于持续、精心的输血、脾切除术以及放弃细胞毒性治疗。观察到病情逐渐、持续发展为原始细胞危象,最终转变为急性白血病。