Rabasa P, Domingo J M, Quílez D, Monzón F
Servicio de Hematología, Hospital Reina Sofía, Tudela, Navarra.
Sangre (Barc). 1998 Jun;43(3):240-3.
Ki-1 anaplastic large cell lymphoma is a well-described subtype of non-Hodgkin's lymphoma with distinctive characteristics from the cytological, immunohistochemical and clinical points of view. One of the clinical behavior characteristic is that it rarely evolves into a leukaemic phase. We report the case of a 72-year-old man in which the appearance of tumor cells in peripheral blood was one of the most revealing information. The patient showed B-symptoms, bicytopenia and bone marrow involvement, together with hepatosplenomegaly and right axilar adenopathy, which after biopsied lead to Ki-1 anaplastic large cell lymphoma's diagnosis (stage IV-B). As far as the treatment and evolution are concerned, we choose a polychemotherapy (ACOP-B) because of the patient's age. Up to now clinical and analitical course is excellent and the patient is now in remission.
Ki-1间变性大细胞淋巴瘤是一种已被充分描述的非霍奇金淋巴瘤亚型,从细胞学、免疫组织化学和临床角度来看具有独特特征。其临床行为特征之一是很少演变为白血病期。我们报告了一名72岁男性的病例,外周血中出现肿瘤细胞是最具揭示性的信息之一。该患者表现出B症状、全血细胞减少和骨髓受累,伴有肝脾肿大和右腋窝淋巴结病,活检后诊断为Ki-1间变性大细胞淋巴瘤(IV-B期)。就治疗和病程而言,由于患者年龄因素,我们选择了多药化疗(ACOP-B)。到目前为止,临床和分析过程良好,患者目前处于缓解期。