Finn William G, Sreekumar Arun, Menon Anjana, Utiger Cheryl, Chinnaiyan Arul
University of Michigan Medical School, Ann Arbor, MI, USA.
Leuk Lymphoma. 2006 Jan;47(1):121-7. doi: 10.1080/10428190500259983.
Trisomy 12 can be seen in many different lymphoid neoplasms. However, many or most mature B-cell leukemias associated with isolated trisomy 12 are reported in the literature as chronic lymphocytic leukemia (CLL) or 'atypical CLL'. This study reports a case of a mature B-cell leukemia, morphologically and immunophenotypically similar to cases previously published as atypical CLL, in which cytogenetic evaluation revealed an isolated clonal trisomy 12 but no evidence of the mantle cell lymphoma-associated t(11;14)(q13;q32). Further analysis confirmed absence of cyclin-D1 expression. Subsequent lymph node biopsy revealed evidence of large cell transformation of the underlying chronic lymphoproliferative disorder. Gene expression profiling of the initial peripheral blood sample using a cDNA micro-array of approximately 10,000 expressed genes revealed a close resemblance between the reported case and 2 cases of known mantle cell lymphoma. When further compared to 7 known 'typical' CLL cases, the reported case was classified as mantle cell lymphoma by hierarchical cluster analysis. The case reported here raises interesting questions regarding the nature of cases reported previously as trisomy 12-associated CLL and reinforces the fact that other leukemic lymphoproliferative disorders should be included in the differential diagnosis of such cases. Further study is indicated to elucidate the nature and diversity of disorders previously reported as trisomy 12-associated chronic lymphocytic leukemia.
12号染色体三体可见于多种不同的淋巴样肿瘤。然而,文献报道中许多或大多数与孤立性12号染色体三体相关的成熟B细胞白血病被诊断为慢性淋巴细胞白血病(CLL)或“非典型CLL”。本研究报告了1例成熟B细胞白血病病例,其形态学和免疫表型与先前报道的非典型CLL病例相似,细胞遗传学评估显示存在孤立的克隆性12号染色体三体,但未发现与套细胞淋巴瘤相关的t(11;14)(q13;q32)。进一步分析证实不存在细胞周期蛋白D1表达。随后的淋巴结活检显示存在基础慢性淋巴细胞增殖性疾病的大细胞转化证据。使用约10000个表达基因的cDNA微阵列对初始外周血样本进行基因表达谱分析,结果显示该病例与2例已知的套细胞淋巴瘤病例极为相似。当与7例已知的“典型”CLL病例进一步比较时,通过层次聚类分析,该病例被归类为套细胞淋巴瘤。本文报道的病例引发了关于先前报道的与12号染色体三体相关的CLL病例性质的有趣问题,并强化了一个事实,即其他白血病性淋巴细胞增殖性疾病应纳入此类病例的鉴别诊断。需要进一步研究以阐明先前报道的与12号染色体三体相关的慢性淋巴细胞白血病的疾病性质和多样性。