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Japanese case of follicular lymphoma of ocular adnexa diagnosed by clinicopathologic, immunohistochemical, and molecular genetic techniques

机译:通过临床病理,免疫组织化学和分子遗传技术诊断出的日本人眼附件的滤泡性淋巴瘤病例

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Background: Follicular lymphomas of the ocular adnexa are very rare in Japan, with only two reported cases.Case: A 44-year-old woman visited our clinic for treatment of ocular adnexal tumors in both eyes.Findings: Histologic examination showed that the neoplastic lesions consisted of atypical lymphoid cells, and the tentative diagnosis was malignant lymphoma. Immunophenotypic analyses by flow cytometry and immunohistochemistry showed that the atypical lymphoid cells expressed CD45, bcl-2, CD10, CD19, CD20, IgM, and kappa light chains. The cells were negative for CD5 and other T, natural killer, or myelomonocyte antigens. Southern blot hybridization demonstrated gene rearrangement bands in the immunoglobulin JH region. Fluorescence in situ hybridization studies showed a translocation at t(14,18)(q32,q21). Systemic evaluations detected enlargements of both the inguinal lymph nodes and parabronchial lymph nodes.Conclusion: Our results show that flow cytometry, molecular genetic analyses, and chromosomal examination can be useful in differentiating follicular lymphoma from marginal zone B cell lymphoma of mucosa-associated lymphoid tissue and reactive lymphoid hyperplasia.
机译:背景:眼部附件的滤泡性淋巴瘤在日本非常罕见,仅报道了两例。病例:一名44岁的妇女前往我们的诊所治疗两只眼睛的眼部附件肿瘤。发现:组织学检查显示为赘生物病变由非典型淋巴样细胞组成,初步诊断为恶性淋巴瘤。通过流式细胞术和免疫组织化学的免疫表型分析表明,非典型淋巴样细胞表达CD45,bcl-2,CD10,CD19,CD20,IgM和κ轻链。这些细胞对CD5和其他T,自然杀伤分子或骨髓细胞抗原呈阴性。 Southern印迹杂交证实了免疫球蛋白JH区域中的基因重排带。荧光原位杂交研究表明在t(14,18)(q32,q21)易位。系统评价发现腹股沟淋巴结和支气管旁淋巴结均增大。和反应性淋巴增生。

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