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首页> 外文期刊>British Journal of Medicine and Medical Research >Primary Small B-cell Lymphoma (MALT Lymphoma) at Lingual Tonsil: A Case Report
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Primary Small B-cell Lymphoma (MALT Lymphoma) at Lingual Tonsil: A Case Report

机译:扁桃体扁桃体原发性小B细胞淋巴瘤(MALT淋巴瘤):一例报告

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Aims: Primary non-Hodgkin’s lymphomas of the oropharyngeal region are rare. We report a case of a small B-cell lymphoma (MALT lymphoma) involving base of tongue. The patient was successfully treated with wide excision of the lesion followed by radiotherapy. Presentation of Case: A 75-year-old female Caucasian patient was referred to our clinic with complaints of foreign body sensation in the throat and progressively worsening snoring over 4 months. Oropharyngeal examination revealed a 3x3-cm smooth mass originating from the left side of the base of tongue and moving with protrusion of the tongue. Excisional biopsy revealed a low-grade small B-cell lymphoma with lambda monoclonal plasmacytic differentiation [extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT) with lambda monoclonal plasmacytic differentiation]. The neoplastic population was consisted of small lymphoid B-cells and lambda monoclonal plasma cells. Lymphoid cells showed CD20(+), CD5(-), CD23(-), CD10(-), BCL-6(-), IgD(-), BCL-2(+). In the neoplasm were seen few mitoses, and cellular proliferation marker Ki-67 was approximately 15%. Magnetic resonance imaging of the head and neck showed a well-circumscribed solid mass originating from the base of left side tongue. Bone marrow aspiration biopsy showed no evidence of disease. Computerized tomographic scans of the thorax and magnetic resonance imaging of the abdomen showed no adenopathy. Tumor was determined to be at Stage I. Discussion and Conclusion: Primary non-Hodgkin’s lymphomas involving oropharyngeal region should be considered in differential diagnosis of all lesions located in this region. To our knowledge, a case of small B-cell lymphoma of the base of the tongue is rarely reported. An appropriate evaluation of the clinical presentation along with histopathologic and immunohistochemical evaluation of biopsy specimen may aid in the diagnosis and effective treatment.
机译:目的:口咽区原发性非霍奇金淋巴瘤很罕见。我们报告了一例涉及舌根的小B细胞淋巴瘤(MALT淋巴瘤)。广泛切除病灶,然后放疗成功地治疗了该患者。病例介绍:一名75岁的白种人女性患者因喉咙异物感和在4个月内逐渐打而转诊至我们的诊所。口咽检查显示有一个3x3厘米的光滑块,从舌根的左侧开始,随舌头的突出而移动。切除活检显示低级小B细胞淋巴瘤具有lambda单克隆浆细胞性分化[黏膜相关淋巴组织(MALT)的膜外边缘区淋巴瘤具有lambda单克隆浆细胞性分化]。肿瘤人群由小的淋巴B细胞和λ单克隆浆细胞组成。淋巴样细胞显示CD20(+),CD5(-),CD23(-),CD10(-),BCL-6(-),IgD(-),BCL-2(+)。在肿瘤中几乎看不到有丝分裂,而细胞增殖标记物Ki-67约为15%。头部和颈部的磁共振成像显示出来自左侧舌根的良好包围的固体块。骨髓穿刺活检未显示疾病证据。胸部计算机断层扫描和腹部磁共振成像均未发现腺病。肿瘤被确定为处于第一阶段。讨论与结论:在鉴别诊断位于该区域的所有病变时,应考虑原发性非霍奇金淋巴瘤涉及口咽区域。据我们所知,很少有舌根部小B细胞淋巴瘤病例的报道。临床表现的适当评估以及活检标本的组织病理学和免疫组织化学评估可能有助于诊断和有效治疗。

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