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Cytodiagnosis of primary thyroid lymphoma with histologic correlation: A case report

机译:原发性甲状腺淋巴瘤的细胞学诊断与组织学相关性:一例报告

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摘要

Primary thyroid lymphoma is a very rare disease. Here, we present a case of primary diffuse large B-cell lymphoma (DLBCL) in a 48-year-old female involving thyroid gland. The patient had thyroid swelling for 15 years which rapidly increased during last 5 months. Fine needle aspiration cytology revealed monomorphic large cells arranged discretely. The cells have high nuclear-cytoplasmic ratio with prominent single to multiple nucleoli. Aggregates of thyroid follicular cells were absent in the smears. A cytodiagnosis of DLBCL was made and a differential diagnosis of lymphocytic thyroiditis was also included. Subsequent histologic examination revealed a high-grade non-Hodgkin lymphoma (NHL). Immunohistochemistry showed the tumor cells expressing CD45, CD20, BCl-6, and tumor cells were negative for cytokeratin, epithelial membrane antigen, CD3, CD5, and CD30. Proliferative index (Ki-67) was very high (70%). Thus, a final diagnosis of NHL of DLBCL subtype was established. The patient was treated with R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristin, prednisone) and radiotherapy. The patient is under one-year follow-up which is uneventful.
机译:原发性甲状腺淋巴瘤是一种非常罕见的疾病。在这里,我们介绍了一名48岁的女性甲状腺原发性弥漫性大B细胞淋巴瘤(DLBCL)的病例。该患者甲状腺肿胀持续了15年,在最近5个月中迅速增加。细针穿刺细胞学检查发现单个大细胞离散排列。细胞具有高的核质比,具有突出的单核到多核。涂片中没有甲状腺滤泡细胞聚集体。进行了DLBCL的细胞诊断,还包括淋巴细胞性甲状腺炎的鉴别诊断。随后的组织学检查显示为高度非霍奇金淋巴瘤(NHL)。免疫组织化学显示,表达CD45,CD20,BCl-6的肿瘤细胞对细胞角蛋白,上皮膜抗原,CD3,CD5和CD30呈阴性。增殖指数(Ki-67)很高(70%)。因此,建立了对DLBCL亚型的NHL的最终诊断。该患者接受了R-CHOP(利妥昔单抗,环磷酰胺,阿霉素,长春新碱,泼尼松)和放疗。该患者正在接受一年的随访,很顺利。

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