Kaiser R, Spöttl F
Wien Klin Wochenschr. 1977 Feb 4;89(3):95-8.
The sudden onset of plasma cell leukemia with IgG-lambda-paraproteinaemia is reported in a 59-year-old patient. In the year before clinical manifestation of the disease the patient was examined and treated for a duodenal ulcer and a head injury on three separate occasions in different wards of the hospital without detection of any sign of disease of the haemopoetic system. The clinical features and course of the disease resembled those of acute leukaemia, the maximum percentage of plasma cells in the peripheral blood being 72 and in the bone marrow 98. Osteolytic bone lesions were not observed and there was no renal insufficiency. Therapy with mephelan-prednisolone and cyclophosphamide-prednisolone was not successful in influencing the fatal outcome of the disease.
本文报道了一名59岁患者突发浆细胞白血病并伴有IgG-λ-副蛋白血症。在该疾病临床表现出现的前一年,患者因十二指肠溃疡和头部受伤,在医院不同病房接受了三次检查和治疗,但均未检测到造血系统疾病的任何迹象。该疾病的临床特征和病程与急性白血病相似,外周血中浆细胞的最高百分比为72%,骨髓中为98%。未观察到溶骨性骨病变,也没有肾功能不全。美法仑-泼尼松和环磷酰胺-泼尼松治疗未能成功影响该疾病的致命结局。