Nakamine H, Nishino E, Takenaka T, Maeda J, Kushigami M, Ikeda A, Nishioka S, Yataka I, Hanaoka M
Acta Pathol Jpn. 1986 Nov;36(11):1757-68. doi: 10.1111/j.1440-1827.1986.tb02240.x.
Morphologic and immunological findings found in a patient with immunoblastic lymphadenopathy (IBL)-like T-cell lymphoma (IBL-T) are presented. Though the initial clinical features were suggestive of IBL, multiple cutaneous and visceral tumors appeared later in his course. The cutaneous lesion is considered to be unique, because the neoplastic T cells with suppressor/cytotoxic (S/C) phenotype showed focal epidermotropism, resulting in necrosis and ulceration of the overlying epidermis. An interesting feature in IBL-T is the frequent association of polyclonal hypergammaglobulinemia, yet the neoplastic T cells show S/C phenotype. Since Ia-like antigen was expressed on the neoplastic T cells, it is stressed that antigen-presenting and contrasuppressor cells should also be included in the cell populations which have a possibility to be a normal counterpart of IBL-T.
本文报告了1例具有免疫母细胞性淋巴结病(IBL)样T细胞淋巴瘤(IBL-T)患者的形态学和免疫学发现。尽管最初的临床特征提示为IBL,但在病程后期出现了多发皮肤和内脏肿瘤。皮肤病变被认为是独特的,因为具有抑制/细胞毒性(S/C)表型的肿瘤性T细胞表现出局灶性亲表皮性,导致上方表皮坏死和溃疡。IBL-T的一个有趣特征是多克隆高丙种球蛋白血症频繁出现,然而肿瘤性T细胞表现出S/C表型。由于肿瘤性T细胞上表达了Ia样抗原,强调抗原呈递细胞和抗抑制细胞也应包含在可能是IBL-T正常对应物的细胞群体中。