Banerjee S S, Heald J, Harris M
Department of Histopathology, Christie Hospital and Holt Radium Institute, Manchester.
J Clin Pathol. 1991 Feb;44(2):119-25. doi: 10.1136/jcp.44.2.119.
In seven of 12 cases of Ber-H2 (Ki-1) positive anaplastic large cell non-Hodgkin's lymphoma (Ki-1 ALCL) disease remained localised to skin, and in five there was extracutaneous spread. Four patients had histological evidence of pre-existing or coexisting mycosis fungoides, and three patients had a long standing history of eczema or ichthyosis. In two cases the presence of a T phenotype was shown in frozen sections, and in a further six cases a T phenotype was firmly established in paraffin wax sections. Four patients died less than one year after presentation (two with disseminated lymphoma; two from other causes); one died at five years with widespread lymphoma and the remaining seven cases were alive one to 14 1/2 years after presentation. Three of the four patients with associated mycosis fungoides had prolonged survival, contrary to the findings of previous reports which suggest secondary Ki-1 ALCL behaves aggressively. The recognition of these tumours is important because of their relatively good prognosis. The diagnosis can be readily substantiated immunohistochemically, using a simple panel of antibodies.
在12例Ber-H2(Ki-1)阳性间变性大细胞非霍奇金淋巴瘤(Ki-1 ALCL)中,7例疾病局限于皮肤,5例有皮肤外扩散。4例患者有先前存在或同时存在蕈样肉芽肿的组织学证据,3例患者有长期湿疹或鱼鳞病病史。2例在冰冻切片中显示T表型,另外6例在石蜡切片中明确确定为T表型。4例患者在就诊后不到1年死亡(2例死于播散性淋巴瘤;2例死于其他原因);1例在5年时死于广泛淋巴瘤,其余7例在就诊后1至14.5年存活。4例伴有蕈样肉芽肿的患者中有3例生存期延长,这与先前报告的结果相反,先前报告提示继发性Ki-1 ALCL行为侵袭性。认识到这些肿瘤很重要,因为它们预后相对较好。使用一组简单的抗体,通过免疫组织化学可以很容易地证实诊断。