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1号与14号染色体易位及11号与18号染色体易位在华氏巨球蛋白血症鉴别诊断中的意义

t(1;14) and t(11;18) in the differential diagnosis of Waldenström's macroglobulinemia.

作者信息

Ye Hongtao, Chuang Shih-Sung, Dogan Ahmet, Isaacson Peter G, Du Ming-Qing

机构信息

Department of Pathology, University of Cambridge, UK.

出版信息

Mod Pathol. 2004 Sep;17(9):1150-4. doi: 10.1038/modpathol.3800164.

Abstract

Waldenström's macroglobulinemia is caused by several B-cell proliferative disorders including lymphoplasmacytic lymphoma, marginal zone B-cell lymphoma, B-cell chronic lymphocytic leukemia and multiple myeloma. Differential diagnosis between lymphoplasmacytic lymphoma and extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue is particularly difficult as there is a considerable overlap in histological presentation. We report a case of Waldenström's macroglobulinemia with involvement of the peripheral blood, bone marrow and stomach. Serum chemistry revealed an IgM of 5.4 g/dl, but Bence-Jones protein in urine was negative. Abnormal lymphoid cells were detected in both blood and the bone marrow. Flow cytometry of the bone marrow aspirate showed that majority of cells were CD20(+), CD38(+), expressing immunoglobulin lambda light chain, but CD5(-) and CD10(-). Gastric biopsies revealed infiltration of the gastric mucosa by small lymphoid cells showing plasmacytoid differentiation and occasional Dutcher bodies. Lymphoepithelial lesions and Helicobacter pylori were not seen. Thus, the differential diagnosis between lymphoplasmacytic lymphoma and mucosa-associated lymphoid tissue lymphoma was raised. To resolve this, we performed BCL10 immunohistochemistry and reverse transcriptional polymerase chain reaction (RT-PCR) for the API2-MALT1 fusion transcript of t(11;18)(q21;q21). Both bone marrow and gastric biopsies showed strong BCL10 nuclear staining, similar to that seen in t(1;14)(p22;q32) positive mucosa-associated lymphoid tissue lymphoma, but absence of the API2-MALT1 fusion transcript. To further ascertain whether the detection of t(1;14)(p22;q32) and t(11;18)(q21;q21) can be reliably used for the differential diagnosis between lymphoplasmacytic lymphoma and mucosa-associated lymphoid tissue lymphoma, we screened for these translocations by BCL10 immunohistochemistry in 58 lymphoplasmacytic lymphomas and RT-PCR for t(11;18)(q21;q21) in 40 lymphoplasmacytic lymphomas, respectively. None of the lymphoplasmacytic lymphomas studied harbored these translocations. Thus, detection of t(1;14)(p22;q32) and t(11;18)(q21;q21) is useful in the differential diagnosis between lymphoplasmacytic lymphoma and mucosa-associated lymphoid tissue lymphoma.

摘要

华氏巨球蛋白血症由多种B细胞增殖性疾病引起,包括淋巴浆细胞淋巴瘤、边缘区B细胞淋巴瘤、B细胞慢性淋巴细胞白血病和多发性骨髓瘤。淋巴浆细胞淋巴瘤与黏膜相关淋巴组织的结外边缘区淋巴瘤之间的鉴别诊断特别困难,因为组织学表现有相当大的重叠。我们报告一例累及外周血、骨髓和胃的华氏巨球蛋白血症病例。血清化学检查显示IgM为5.4g/dl,但尿本周蛋白阴性。血液和骨髓中均检测到异常淋巴细胞。骨髓穿刺液的流式细胞术显示,大多数细胞CD20(+)、CD38(+),表达免疫球蛋白λ轻链,但CD5(-)和CD10(-)。胃活检显示胃黏膜有小淋巴细胞浸润,呈浆细胞样分化,偶见杜氏小体。未见淋巴上皮病变和幽门螺杆菌。因此,提出了淋巴浆细胞淋巴瘤与黏膜相关淋巴组织淋巴瘤的鉴别诊断问题。为解决这一问题,我们进行了BCL10免疫组化和针对t(11;18)(q21;q21)的API2-MALT1融合转录本的逆转录聚合酶链反应(RT-PCR)。骨髓和胃活检均显示BCL10核强染色,类似于t(1;14)(p22;q32)阳性黏膜相关淋巴组织淋巴瘤所见,但未检测到API2-MALT1融合转录本。为进一步确定t(1;14)(p22;q32)和t(11;18)(q21;q21)的检测是否可可靠用于淋巴浆细胞淋巴瘤与黏膜相关淋巴组织淋巴瘤的鉴别诊断,我们分别通过BCL10免疫组化对58例淋巴浆细胞淋巴瘤进行了这些易位筛查,并通过RT-PCR对40例淋巴浆细胞淋巴瘤进行了t(11;18)(q21;q21)检测。所研究的淋巴浆细胞淋巴瘤均未携带这些易位。因此,t(1;14)(p22;q32)和t(

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