Horschowski N, Sainty D, Muratore R
Ann Med Interne (Paris). 1983;134(8):739-41.
We report one case of T cell type lymphoma with multilobated nuclei, a distinct variant described by G. Pinkus. The soft palate and subcutaneous tissues were the successive localisations. Despite an aggressive chemotherapy with autologous bone marrow transplantation, a fatal course happened in 18 months. This entity is different from cutaneous lymphomas, mantle zone lymphomas of Waldron, Japanese T lymphomas and from the cases described recently by Weisenburger. The link between these different anatomo-clinical and histological varieties is their belonging to the T cell line.
我们报告一例具有多叶核的T细胞型淋巴瘤,这是一种由G. Pinkus描述的独特变体。软腭和皮下组织是相继出现的病变部位。尽管进行了积极的化疗并联合自体骨髓移植,但患者在18个月内病情呈致命性发展。该实体与皮肤淋巴瘤、Waldron套区淋巴瘤、日本T细胞淋巴瘤以及Weisenburger最近描述的病例不同。这些不同的解剖临床和组织学类型之间的联系在于它们都属于T细胞系。