A transitional variant of a T-lymphoproliferative malignancy. Two cases of cutaneous T-cell lymphoma co-expressing E and Fc gamma receptors with final leukaemic transformation.

Scandinavian journal of haematology Pub Date : 1986-03-01
V Jønsson, G Lange Wantzin, E Badsberg, T Menné, A Videbaek
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Abstract

2 cases of malignant T-lymphoproliferative disease are reported. The proliferating cell was a large blast expressing E and Fc gamma receptors but no helper or suppressor phenotypes and no SmIg. Skin infiltrates were the dominant clinical sign with conspicuous perivascular aggregations of T, E, Fc gamma lymphocytes, though both patients initially had disseminated disease with mild lymphadenopathy, splenomegaly and, in case 2, also hepatic infiltrations. Accordingly, DNA measurements on skin biopsies, taken early in the course, showed a dominating hypotetraploid clone (case 1) and a pronounced population in S-phase (case 2). The patients were alive for 6 and 2 yr, respectively, with a final fatal course of about 6 months duration involving a rather sudden progression of the skin infiltrates, increasing lymphadenopathy and splenomegaly, leukaemic transformation of the neoplastic T, E, Fc gamma lymphocyte and practically no response to cytostatic treatment.

t淋巴增生性恶性肿瘤的一种过渡性变异体。皮肤t细胞淋巴瘤共表达E和Fc受体,最终转化为白血病2例。
本文报告2例恶性t淋巴细胞增生性疾病。增殖细胞是一个大的母细胞,表达E和Fc γ受体,但没有辅助或抑制表型,也没有SmIg。皮肤浸润是主要的临床征象,血管周围有明显的T、E、Fc γ淋巴细胞聚集,但两例患者最初均为弥散性疾病,伴轻度淋巴结病变、脾肿大,病例2也有肝脏浸润。因此,DNA测量皮肤活检,早期过程中,显示出主导hypotetraploid克隆(案例1)和明显的人口s阶段(例2)。这些患者存活6和2年,分别与最后一个致命的6个月时间涉及,而突然恶化皮肤浸润,增加淋巴结病和脾肿大,进展期肿瘤T变换,E,Fc淋巴细胞,对细胞抑制剂治疗几乎没有反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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