Imbing F, Kumar D, Kumar S, Yuoh G, Gardner F
Department of Pathology, University of Texas Medical Branch, USA.
J Clin Pathol. 1995 Jun;48(6):584-7. doi: 10.1136/jcp.48.6.584.
This report describes the occurrence of splenic lymphoma with villous lymphocytes (SLVL) in a 56 year old white female with a family history of chronic lymphocytic leukaemia. Other unusual features included a marked lymphocytosis with counts up to 224 x 10(9)/l and marked clumping of lymphocytes in EDTA anticoagulated blood. The neoplastic cells were CD19+, CD20+, CD22+, CD22+, IgM+, lambda+, kappa-, CD5-, and CD10-. The spleen had nodular infiltrates of B lymphocytes in the region of the white pulp with minimal red pulp involvement. Electron microscopy of peripheral blood lymphocytes revealed cells with polar cytoplasmic processes. This report underlines the need for detailed analysis, including morphology and immunophenotyping, for each patient with a small B cell lymphoproliferative disorder.
本报告描述了一名56岁有慢性淋巴细胞白血病家族史的白人女性发生的伴绒毛淋巴细胞的脾淋巴瘤(SLVL)。其他不寻常特征包括显著的淋巴细胞增多,计数高达224×10⁹/L,以及在乙二胺四乙酸(EDTA)抗凝血液中淋巴细胞明显聚集。肿瘤细胞CD19⁺、CD20⁺、CD22⁺、IgM⁺、λ⁺、κ⁻、CD5⁻和CD10⁻。脾脏白髓区域有B淋巴细胞结节状浸润,红髓受累 minimal。外周血淋巴细胞的电子显微镜检查显示细胞有极性胞质突起。本报告强调对于每例小B细胞淋巴增殖性疾病患者都需要进行包括形态学和免疫表型分析在内的详细分析。