Banerjee S S, Harris M, Eyden B P, Radford J A, Harrison C J, Mainwaring A R
Department of Histopathology, Christie Hospital and Holt Radium Institute, Manchester.
J Clin Pathol. 1991 Jan;44(1):39-44. doi: 10.1136/jcp.44.1.39.
The clinical, light microscopic, ultrastructural, immunocytochemical and cytogenetic features of a case of monocytoid B cell lymphoma were investigated. The tumour initially affected the cervical and supraclavicular nodes, but 33 months later affected the left parotid salivary gland. The patient had subclinical Sjögren's syndrome. The neoplastic cells showed characteristic morphological features and had peri- and interfollicular distribution in the node. Immunocytochemically the tumour cells were L26, 4KB5, MB2, CD19, CD20, CD22 and IgM/kappa positive. Prominent plasmablastic plasmacytoid differentiation was present in the recurrent tumour, suggesting an origin from post-follicular B cells. The lymphoma cells showed unusual cytogenetic abnormalities.
对一例单核细胞样B细胞淋巴瘤的临床、光镜、超微结构、免疫细胞化学和细胞遗传学特征进行了研究。肿瘤最初累及颈部和锁骨上淋巴结,但33个月后累及左侧腮腺。该患者患有亚临床干燥综合征。肿瘤细胞表现出特征性形态学特征,在淋巴结中呈滤泡周围和滤泡间分布。免疫细胞化学显示肿瘤细胞L26、4KB5、MB2、CD19、CD20、CD22和IgM/κ阳性。复发性肿瘤中存在显著的浆母细胞样浆细胞分化,提示起源于滤泡后B细胞。淋巴瘤细胞表现出异常的细胞遗传学异常。