Juneja H S, Rajaraman S, Alperin J B, Bainton D F
Acta Haematol. 1987;77(2):115-9. doi: 10.1159/000205970.
Auer rod-like inclusions (ARLI) can be seen in B cell malignancies but are very rare in prolymphocytic leukemia (PLL). Prolymphocytes with ARLI from a patient with PLL were examined using cytochemical and immunochemical techniques and transmission electronmicroscopy (EM). The lymphoblastic cells gave a positive reaction with antibodies to the gamma heavy chains and kappa light chain. On EM the ARLI were 1-2 micron long, consisting of election-dense crystalline matrix, with a periodicity of 60 A and contained within a single unit membrane. The production of IgG by PLL cells with ARLI has not been previously reported. It is emphasized that in PLL the lymphoblasts can have inclusions resembling Auer rods. Cytochemical and immunochemical studies should be done to avoid a misdiagnosis of acute nonlymphoblastic leukemia.
奥厄小体样包涵体(ARLI)可见于B细胞恶性肿瘤,但在幼淋巴细胞白血病(PLL)中非常罕见。运用细胞化学、免疫化学技术及透射电子显微镜(EM)对1例伴有ARLI的PLL患者的幼淋巴细胞进行了检查。这些淋巴母细胞与抗γ重链和κ轻链抗体呈阳性反应。在电镜下,ARLI长1 - 2微米,由电子致密的结晶基质组成,周期为60埃,且被包裹在单层单位膜内。此前尚未报道过伴有ARLI的PLL细胞产生IgG的情况。需要强调的是,在PLL中,淋巴母细胞可含有类似奥厄小体的包涵体。应进行细胞化学和免疫化学研究以避免误诊为急性非淋巴细胞白血病。