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伴有显著浆细胞增多症和多克隆高球蛋白血症的辅助性T细胞淋巴瘤。病例报告。

Helper T-cell lymphoma with marked plasmacytosis and polyclonal hypergammaglobulinemia. A case report.

作者信息

Tamaki T, Katagiri S, Kanayama Y, Konishi I, Yonezawa T, Tarui S, Kitani T

出版信息

Cancer. 1984 Apr 1;53(7):1590-5. doi: 10.1002/1097-0142(19840401)53:7<1590::aid-cncr2820530728>3.0.co;2-c.

Abstract

A case of malignant lymphoma with a helper activity of neoplastic cells is reported. On admission, a significant number of plasma cells of polyclonal nature were seen in the peripheral blood, and polyclonal hypergammaglobulinemia was seen. The biopsied lymph node showed poorly differentiated lymphocytic lymphoma with marked proliferation of plasma cells. At the terminal stage, the patient became leukemic in contrast with the disappearance of plasma cells from the peripheral blood. Although the leukemic cells failed to form sheep erythrocyte rosettes, they were considered to be of T-cell origin morphologically. Cytochemically, they had a "dot"-like pattern of alpha-naphthyl acetate esterase and acid phosphatase activity. Ultrastructurally, they had highly convoluted nuclei, and cytoplasmic clustered dense bodies. They showed marked helper activity on pokeweed mitogen-induced B-cell differentiation in vitro. This case may provide a novel view concerning the cause of hypergammaglobulinemia induced by lymphoproliferative disorders.

摘要

报告了一例具有肿瘤细胞辅助活性的恶性淋巴瘤病例。入院时,外周血中可见大量多克隆性质的浆细胞,并出现多克隆高球蛋白血症。活检的淋巴结显示为低分化淋巴细胞性淋巴瘤,伴有浆细胞明显增生。在终末期,患者发生白血病,与此同时外周血中的浆细胞消失。尽管白血病细胞不能形成绵羊红细胞玫瑰花结,但从形态学上考虑它们起源于T细胞。细胞化学检查显示,它们具有α-萘乙酸酯酶和酸性磷酸酶活性的“点状”模式。超微结构上,它们有高度卷曲的细胞核和细胞质聚集的致密小体。它们在体外对商陆有丝分裂原诱导的B细胞分化表现出明显的辅助活性。该病例可能为淋巴增殖性疾病引起的高球蛋白血症的病因提供新的观点。

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