Sato M, Ishikawa O, Miyachi Y
Department of Dermatology, Gunma University School of Medicine, Japan.
Br J Dermatol. 1995 Nov;133(5):810-3. doi: 10.1111/j.1365-2133.1995.tb02764.x.
A 52-year-old man with cutaneous T-cell lymphoma presented with Sézary syndrome-like features including exfoliative erythroderma, lymphadenopathy and leukaemic change without the presence of Sézary cells. Southern blot hybridization analysis revealed T-cell receptor beta-chain gene rearrangements, both in the peripheral blood and in the lymph node. Atypical large cells with convoluted nuclei (Sézary-like cells) first appeared during combined chemotherapy. Although Sézary syndrome is characterized by its particular manifestations and the presence of Sézary cells in the peripheral blood, the clinical significance of Sézary cells has been questioned. It still needs to be decided whether or not the Sézary cell is malignant.
一名52岁的皮肤T细胞淋巴瘤男性患者出现了类似塞扎里综合征的特征,包括剥脱性红皮病、淋巴结病和白血病样改变,但外周血中不存在塞扎里细胞。Southern印迹杂交分析显示,外周血和淋巴结中均存在T细胞受体β链基因重排。在联合化疗期间首次出现了具有卷曲核的非典型大细胞(类塞扎里细胞)。尽管塞扎里综合征以其特定表现和外周血中存在塞扎里细胞为特征,但塞扎里细胞的临床意义一直受到质疑。塞扎里细胞是否为恶性仍有待确定。