Huh Hee Jin, Min Hyun Chung, Cho Han Ik, Chae Seok Lae, Lee Dong Soon
Department of Laboratory Medicine, Dongguk University, College of Medicine, Siksa-dong, Ilsandong-gu, Goyang, Gyeonggi-do, Republic of Korea.
Cancer Genet Cytogenet. 2008 Oct;186(1):1-5. doi: 10.1016/j.cancergencyto.2008.04.012.
We evaluated the usefulness of interphase fluorescence in situ hybridization (FISH) for the detection of bone marrow involvement of lymphoma, comparing the results with those of microscopic examination. Bone marrow aspirates obtained for staging work-up from 150 patients with non-Hodgkin lymphoma were used in this study. Interphase FISH study using four probes and conventional G-banding were performed on bone marrow aspirates. The four probes included locus specific identifier (LSI) immunoglobulin heavy chain (IGH) dual-color break-apart rearrangement probe, an LSI p16 SpectrumOrange/CEP 9 SpectrumGreen probe, an LSI BCL6 dual-color break-apart rearrangement probe. Among 150 cases, 29 cases (19.3%) showed infiltration of neoplastic lymphoid cells by microscopic examination. Chromosomal aberrations were detected by FISH in eight patients and by conventional cytogenetic study in three patients. FISH study showed 14q32 rearrangement in four patients (4/126, 3.2%), 9q21 rearrangement in no patients (0/144, 0%), 3q27 rearrangement in four patients (4/131. 3.1%), and a gain of 1q21q32 in two patients (2/115, 1.7%). Among eight patients with abnormal FISH patterns, six had normal karyotypes or no analyzable metaphase according to the conventional cytogenetic study. Seven patients with FISH abnormality showed bone marrow involvement of lymphoma by microscopic examination. One patient, who was defined as having no evidence of bone marrow involvement by microscopic examination, showed a 3q27 aberration in the FISH study. Although the number of patients with BM involvement that was detected by FISH was low, abnormal FISH patterns were detected in six patients who did not have abnormal karyotypes. Therefore, FISH analysis would be beneficial in cytogenetic diagnosis and follow-up study of minimal residual diseases, once the cytogenetic changes are detected at initial diagnosis.
我们评估了间期荧光原位杂交(FISH)在检测淋巴瘤骨髓受累情况方面的实用性,并将结果与显微镜检查结果进行了比较。本研究使用了从150例非霍奇金淋巴瘤患者分期检查时获取的骨髓抽吸物。对骨髓抽吸物进行了使用四种探针的间期FISH研究和传统的G显带分析。这四种探针包括位点特异性标识符(LSI)免疫球蛋白重链(IGH)双色断裂分离重排探针、LSI p16 SpectrumOrange/CEP 9 SpectrumGreen探针、LSI BCL6双色断裂分离重排探针。在150例病例中,显微镜检查显示29例(19.3%)存在肿瘤性淋巴细胞浸润。通过FISH在8例患者中检测到染色体畸变,通过传统细胞遗传学研究在3例患者中检测到染色体畸变。FISH研究显示,4例患者(4/126,3.2%)存在14q32重排,无患者(0/144,0%)存在9q21重排,4例患者(4/131,3.1%)存在3q27重排,2例患者(2/115,1.7%)存在1q21q32增益。在8例FISH模式异常的患者中,根据传统细胞遗传学研究,6例患者核型正常或无可分析的中期分裂相。7例FISH异常的患者显微镜检查显示有淋巴瘤骨髓受累。1例显微镜检查定义为无骨髓受累证据的患者,FISH研究显示存在3q27畸变。虽然通过FISH检测到的骨髓受累患者数量较少,但在6例核型正常的患者中检测到了异常的FISH模式。因此,一旦在初始诊断时检测到细胞遗传学改变,FISH分析将有助于细胞遗传学诊断和微小残留病的随访研究。