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库特纳瘤(慢性硬化性涎腺炎)区域淋巴结的淋巴浆细胞浸润:3例报告

Lymphoplasmacytic infiltrate of regional lymph nodes in Kuttner's tumor (chronic sclerosing sialadenitis): a report of 3 cases.

作者信息

Kojima Masaru, Miyawaki Shuichi, Takada Satoru, Kashiwabara Kenji, Igarashi Tadahiko, Nakamura Shigeo

机构信息

Department of Pathology and Clinical Laboratories, Gunma Center Hospital, Ohta, Japan.

出版信息

Int J Surg Pathol. 2008 Jul;16(3):263-8. doi: 10.1177/1066896907306969.

Abstract

Regional lymph nodes of Küttner's tumor from 3 patients showed reactive follicular hyperplasia and prominent interfollicular plasmacytosis. The patients were 71-, 57-, and 73-year-old Japanese men. The polytypic nature of plasma cells was demonstrated by immunohistochemistry. There were numerous IgG-positive plasma cells with scattered IgA-positive or IgM-positive plasma cells. IgG4-positive cells comprised 25% to 40% of IgG-positive plasma cells. Prominent polyclonal hyperimmunoglobulinemia was demonstrated on laboratory test in 2 cases examined. An elevated serum IgG4 level (16%) was also demonstrated in 1 patient. The present 3 cases indicated that regional lymph node of Küttner's tumor may show reactive follicular hyperplasia and prominent interfollicular plasmacytosis and should be differentiated from various benign and malignant lymphoproliferative disorders including systemic rheumatic disease, plasma cell type of Castleman disease, and lymph node involvement of marginal B-cell lymphoma of the mucosa-associated lymphoid tissue type showing prominent plasma cell differentiation.

摘要

3例Küttner瘤患者的区域淋巴结显示反应性滤泡增生和显著的滤泡间浆细胞增多。患者为71岁、57岁和73岁的日本男性。免疫组化显示浆细胞具有多型性。有大量IgG阳性浆细胞,散在分布着IgA阳性或IgM阳性浆细胞。IgG4阳性细胞占IgG阳性浆细胞的25%至40%。在2例接受检查的病例中,实验室检查显示有显著的多克隆高免疫球蛋白血症。1例患者血清IgG4水平也升高(16%)。目前这3例病例表明,Küttner瘤的区域淋巴结可能显示反应性滤泡增生和显著的滤泡间浆细胞增多,应与各种良性和恶性淋巴增殖性疾病相鉴别,包括系统性风湿性疾病、Castleman病浆细胞型以及黏膜相关淋巴组织型边缘B细胞淋巴瘤的淋巴结受累,后者表现出显著的浆细胞分化。

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