Mansoor A, Medeiros L J, Weber D M, Alexanian R, Hayes K, Jones D, Lai R, Glassman A, Bueso-Ramos C E
Department of Hematopathology, University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX 77030, USA.
Am J Clin Pathol. 2001 Oct;116(4):543-9. doi: 10.1309/6U88-357U-UKJ5-YPT3.
We correlated bone marrow cytogenetic findings with morphologic and immunophenotypic data in 37 patients with lymphoplasmacytic lymphoma (LPL)/Waldenström macroglobulinemia (WM). Each LPL/WM case was classified as lymphoplasmacytoid (n = 18), lymphoplasmacytic (n = 10), or polymorphous (n = 9) using the Kiel criteria. Of 12 cases with chromosomal abnormalities, a single numeric abnormality was present in 4 and a complex karyotype in 8. The most common numeric abnormalities were and -8 in 3 cases each; the most common structural abnormality was del(6q) in 6 cases. Cytogenetic abnormalities were significantly less common in the lymphoplasmacytic and lymphoplasmacytoid groups (5/28 [18%]) compared with the polymorphous group (7/9 [78%]). Clinical follow-up was available for 28 patients for a median of 36 months. Six (67%) of 9 patients with aneuploid tumors, including 4 with polymorphous subtype, subsequently had clinical progression or developed high-grade lymphoma. In contrast, 4 (21%) of 19 patients with diploid tumors, including 1 of polymorphous type, developed clinical progression or high-grade lymphoma. We conclude that abnormal cytogenetic findings in LPL/WM correlate with the polymorphous subtype and poor prognosis.
我们将37例淋巴浆细胞淋巴瘤(LPL)/华氏巨球蛋白血症(WM)患者的骨髓细胞遗传学结果与形态学和免疫表型数据进行了关联分析。根据 Kiel 标准,每例LPL/WM病例被分类为淋巴浆细胞样(n = 18)、淋巴浆细胞性(n = 10)或多形性(n = 9)。在12例存在染色体异常的病例中,4例存在单一数值异常,8例存在复杂核型。最常见的数值异常是 和 -8,各有3例;最常见的结构异常是del(6q),有6例。与多形性组(7/9 [78%])相比,淋巴浆细胞性和淋巴浆细胞样组的细胞遗传学异常明显较少见(5/28 [18%])。对28例患者进行了临床随访,中位随访时间为36个月。9例非整倍体肿瘤患者中有6例(67%),包括4例多形性亚型患者,随后出现临床进展或发展为高级别淋巴瘤。相比之下,19例二倍体肿瘤患者中有4例(21%),包括1例多形性类型患者,出现临床进展或高级别淋巴瘤。我们得出结论,LPL/WM中异常的细胞遗传学结果与多形性亚型及不良预后相关。