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作 者:任国平[1] 余心如[1] 许亮文 尹鲁生 黄东胜[1]
机构地区:[1]浙江医科大学附一院病理科,浙医大杭州分校,浙医大附一院普外科
出 处:《诊断病理学杂志》1996年第2期85-87,共3页Chinese Journal of Diagnostic Pathology
摘 要:本文分析了10例原发性甲状腺恶性淋巴瘤(TL)及86例淋巴细胞性甲状腺炎(LT)的临床病理特征。对其中11例重度LT及TL作了免疫标记。TL中8例为B细胞性,2例为T细胞性;7例见淋巴上皮病损,3例见明显甲状腺外浸润,5例TL残留组织中见LT背景,2例符合结外边缘带B细胞淋巴瘤。11例重度LT中见淋巴细胞内陷于滤泡上皮间,免疫标记示免疫球蛋白轻链多克隆性。本文讨论了甲状腺粘膜相关组织淋巴瘤的病理特征及TL的诊断标准问题,提出TL与LT有密切关系,TL可能来自原发存在的LT。cases of primary thyroid malignant lymphoma and 11 severe cases with thyroiditis selected from 96 specimens of throidectomies were studied. Histologically,there were lymphoepithelial lesions, heterogeneous lymphocyte infiltration, destruction of thyroid structure and focal necrosis in thyroid lymphoma.Immune labelling showed monoclonal light chain in nature. There were 2 cases with extranodal marginal zone B-cell lymphoma constituted chiefly by centrocyte-like cells growing around the follicle with significant lymphoepithelial lesions, their prognoses being relatively good. The analysis reveals that the occurrence of thyroid lymphoma is closely related to lymphocytic thyroiditis. Most thyroid lymphoma and mucosa-associated lymphoid tissue-malignant lymphoma (MALT-ML) in other parts of the body have common immune labelling characteristics. The cells in thyroid lymphoma probably are derived from the parafollicular B-cells,and the low grade malignancy possibly can transform into high malignancy. The prognosis not only depends on the pathological gradation, but also on the clinical stage of the disease.
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