原发性甲状腺淋巴瘤:粘膜相关淋巴组织淋巴瘤病例

U. Alabalık, A. Keleş, G. Türkçü, M. Kuçukoner, Y. Avcı, H. Büyükbayram
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引用次数: 1

摘要

原发性甲状腺淋巴瘤是仅局限于甲状腺或甲状腺及其周围淋巴结的淋巴瘤。这些通常是粘膜相关淋巴组织(MALT)淋巴瘤,起源于B细胞。我们的病例是一位78岁的女性患者,她因颈部肿块而入院,并因怀疑恶性肿瘤而手术。组织病理学检查显示非典型淋巴样细胞弥漫性增生,由小到中等大小的细胞组成,细胞核轮廓不规则,其中一些类似于中心细胞。免疫组化染色CD20、CD79alpha、CD43和lambda阳性,CD3、CD30、CD15、bcl-2、bcl-6、CD68、CD138、CD5和CD10阴性。根据这些发现,该病例被认为是“原发性甲状腺MALT淋巴瘤”。甲状腺MALT淋巴瘤的特点是存在起源于淋巴滤泡边缘区域的非典型淋巴细胞。免疫组织化学上,虽然这些淋巴瘤表达B细胞相关抗体(CD20、CD22、CD79a),但未见相反的CD5、CD10和CD3表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary thyroid lymphoma: mucosa associated lymphoid tissue lymphoma case -
Primary thyroid lymphomas are lymphomas which are localized only to thyroid gland or thyroid gland and surrounding lymph nodes. Frequently these are mucosa associated lymphoid tissue (MALT) lymphomas with B cell origin. Our case is a 78-year-old female patient who admitted with a neck mass and had been operated with the suspicion of malignancy. Histopathological examination revealed diffuse proliferation of atypical lymphoid cells that consists of small to medium sized cells, with irregular nuclear contours, some of which resemble centrocytes. Immunohistochemical staining was positive for CD20, CD79alpha, CD43, and lambda while negative for CD3, CD30, CD15, bcl-2, bcl-6, CD68, CD138, CD5, and CD10. With these finding, the case was considered as “primary thyroid MALT lymphoma”. Thyroid MALT lymphomas are characterized with the presence of atypical lymphocytes that originate from the marginal zones of lymhoid follicles. Immunohistochemically, while these lymphomas express the B cell associated antibodies (CD20, CD22, CD79a), conversely CD5, CD10, and CD3 expressions are not seen.
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