Berrebi A, Talmor M, Vorst E, Resnitzky P, Shtalrid M
Scand J Haematol. 1983 Jan;30(1):43-9. doi: 10.1111/j.1600-0609.1983.tb00633.x.
In a 64-year-old female with chronic lymphocytic leukaemia, nearly 50% of the lymphocytes presented one or several globular intracytoplasmic inclusions resembling Russell bodies which were characterized by immunofluorescence as IgM lambda. On electron microscopy, the inclusions looked like cisternae of the rough endoplasmic reticulum. Surface membrane Ig was not detected and the serum IgM was low. The histology of a lymph node showed a lymphocytic proliferation with evidence of Ig synthesis, compatible with immunocytoma. The aggressive course of the disease necessitated polychemotherapy. This case represents an unusual ill-defined lymphoproliferative disorder, lying between the B-CLL and a non-secretory macroglobulinaemia.
在一名64岁的慢性淋巴细胞白血病女性患者中,近50%的淋巴细胞呈现出一个或多个类似拉塞尔小体的球形胞质内包涵体,免疫荧光显示其特征为IgM λ。电子显微镜下,这些包涵体看起来像粗面内质网的池。未检测到表面膜免疫球蛋白,血清IgM水平较低。淋巴结组织学检查显示淋巴细胞增殖并有免疫球蛋白合成的证据,符合免疫细胞瘤。疾病的侵袭性病程需要进行多药化疗。该病例代表了一种不寻常的、定义不明确的淋巴增殖性疾病,介于B细胞慢性淋巴细胞白血病和非分泌性巨球蛋白血症之间。