Karube Kennosuke, Ohshima Koichi, Tsuchiya Takeshi, Yamaguchi Takahiro, Kawano Riko, Suzumiya Junji, Harada Mine, Kikuchi Masahiro
Department of Pathology, School of Medicine, Fukuoka University, Fukuoka 814-0180, Japan.
Hum Pathol. 2005 Feb;36(2):202-6. doi: 10.1016/j.humpath.2004.12.010.
We describe 6 cases of a specific variant of nodal marginal zone lymphoma with "floral" lymph follicles in patients ranging in age from 18 to 66 years. All 6 patients had lymphadenopathy, either local (n = 5) or systemic (n = 1), and good performance status (0), and none had fever, weight loss, or night sweating. They all underwent excisional biopsy. Histologically, all lesions had a distinctive morphology, with proliferation of medium-sized atypical lymphoid cells in the marginal zone, hyperplastic lymph follicles with enlarged germinal centers, and a thickened mantle zone. In places, folliculolysis was observed. On immunohistochemical staining, the atypical lymphoid cells showed a B-cell phenotype (CD20 +), IgM positivity in 2 of 5 cases, and negativity for CD5, CD10, CD23, CD43, bcl-6, and IgD. Polymerase chain reaction examination for immunoglobulin heavy chain in 5 cases showed monoclonality in all. Five patients did not receive adjuvant chemotherapy and had no recurrences. The patient with systemic lymphadenopathy received chemotherapy and had a complete response without relapse. This variant should be differentiated from the usual nodal marginal zone lymphoma because of its specific clinical and pathological features.
我们描述了6例年龄在18至66岁之间的伴有“花环状”淋巴滤泡的结节性边缘区淋巴瘤特定变异型患者。所有6例患者均有淋巴结病,局部淋巴结病5例,全身淋巴结病1例,且一般状况良好(0),均无发热、体重减轻或盗汗。他们均接受了切除活检。组织学上,所有病变均有独特的形态,边缘区有中等大小非典型淋巴细胞增殖,生发中心扩大的增生性淋巴滤泡,以及增厚的套区。部分区域可见滤泡溶解。免疫组化染色显示,非典型淋巴细胞呈B细胞表型(CD20 +),5例中有2例IgM阳性,CD5、CD10、CD23、CD43、bcl-6和IgD均为阴性。5例患者进行免疫球蛋白重链的聚合酶链反应检测,均显示单克隆性。5例患者未接受辅助化疗,无复发。全身淋巴结病患者接受化疗,完全缓解且无复发。由于其特定的临床和病理特征,该变异型应与常见的结节性边缘区淋巴瘤相鉴别。