Nezelof C
Bull Mem Acad R Med Belg. 1992;147(11-12):472-8; discussion 478-80.
The anaplastic large cell, CD30 positive lymphomas represent a heterogeneous group of lymphomas in which immunocytochemical and molecular investigations have demonstrated the existence of malignancies of T, B or undetermined origin. The recent identification, in a few cases of this group of a chromosomal 5q35 breakpoint may allow the individualization of a peculiar disease entity. In these cases, the 5q35bp has been found to be a permanent abnormality, present in five human permanent cell lines and associated with various translocations including t(2;5), t(1;5) and t(5;6). A primitive myelo-monocytic origin of these 5q35bp cell is suggested on the basis of the following arguments: they express the c-fms proto-oncogene which encodes the macrophage growth receptor (CSF-1-R) the c-fms is mapped on 5q33,34 close to the 5q35bp the express spontaneously CD68 the treatment by phorbol-diester of a 5q35bp cell line (DEL cell line) induces an immunodependent phagocytosis and a modulation of expression of c-fms, CSF-1 and TNF alpha. Because some 5q35bp cell lines also presents rearrangements for TCR-bêta, or IgF, these data suggest an ancestral stem cell origin, prior to the T, B and myelomonocytic differentiation. Whatever its origin, the 5q35bp abnormality has been mainly encountered in children's malignancies. It has been constantly associated with clinical and biological manifestations of a condition recognized by paediatricians as malignant histiocytosis. For this reason, the 5q35bp may today represent the best criterion for the identification of malignant histiocytosis in childhood.
间变性大细胞、CD30阳性淋巴瘤是一组异质性淋巴瘤,免疫细胞化学和分子研究表明其存在T细胞、B细胞或来源未明的恶性肿瘤。最近在该组的少数病例中发现的染色体5q35断点,可能使一种特殊的疾病实体得以个体化。在这些病例中,5q35bp被发现是一种永久性异常,存在于5个人类永久细胞系中,并与包括t(2;5)、t(1;5)和t(5;6)在内的各种易位相关。基于以下论据提示这些5q35bp细胞起源于原始髓单核细胞:它们表达c-fms原癌基因,该基因编码巨噬细胞生长受体(CSF-1-R),c-fms定位于5q33,34,靠近5q35bp;它们自发表达CD68;用佛波酯处理一个5q35bp细胞系(DEL细胞系)可诱导免疫依赖性吞噬作用以及c-fms、CSF-1和TNFα表达的调节。因为一些5q35bp细胞系也存在TCR-β或IgF的重排,这些数据提示其起源于T、B和髓单核细胞分化之前的祖干细胞。无论其起源如何,5q35bp异常主要见于儿童恶性肿瘤。它一直与儿科医生所认识的一种疾病的临床和生物学表现相关,这种疾病被称为恶性组织细胞增多症。因此,5q35bp如今可能是儿童恶性组织细胞增多症诊断的最佳标准。