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[原发性干燥综合征合并非霍奇金淋巴瘤患者的特征:9例分析]

[Characteristics of patients with primary Sjögren's syndrome and non-Hodgkin's lymphoma: analysis of 9 cases].

作者信息

Jia Ning, Tang Fu-Lin

机构信息

Department of Medical Oncology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2009 Oct 27;89(39):2786-8.

Abstract

OBJECTIVE

To characterize the clinical patterns of expression, laboratory serologic parameters and lymphomatous histological characteristics in patients with primary Sjögren's syndrome (pSS) who subsequently developed non-Hodgkin's lymphoma (NHL).

METHODS

The authors analyzed 9 pSS patients (8 females, 1 male) who developed NHL. Five patients had received glucocorticoids, four of whom had received at least one immunosuppressive drugs (methotrexate, glucosidorum tripterygll totorum, cyclophosphamide and imuran). A protocol form was used to record the main characteristics of pSS and NHL.

RESULTS

Eight patients fulfilled the American-European Consensus Criteria (AECC). The main SS manifestations were painless parotid enlargement (n = 7), six of whom were unilateral; the main immunologic features were positive rheumatoid factor (RF) in all examined patients and hyperimmunoglobulinemia (n = 7). The main manifestations of NHL were splenomegaly (n = 7) and lymphadenopathy (n = 5). The main histological subtypes were mucosa-associated lymphoid tissue (MALT) lymphoma (n = 4) and diffuse large B cell lymphoma (n = 2). None of the patients with MALT lymphoma had a nodal primary location. Eight patients had an extranodal primary location, most frequently in salivary gland (n = 4) and lung (n = 4).

CONCLUSION

Patients with pSS and NHL are clinically characterized by a high frequency of painless unilateral parotid enlargement, splenomegaly, lymphadenopathy, an immunologic pattern dominated by the presence of high-titer RF and hyperimmunoglobulinemia, a predominance of MALT lymphomas and an elevated frequency of primary extranodal involvement.

摘要

目的

描述原发性干燥综合征(pSS)患者随后发生非霍奇金淋巴瘤(NHL)的临床表达模式、实验室血清学参数和淋巴瘤组织学特征。

方法

作者分析了9例发生NHL的pSS患者(8例女性,1例男性)。5例患者接受过糖皮质激素治疗,其中4例接受过至少一种免疫抑制药物(甲氨蝶呤、雷公藤多苷、环磷酰胺和硫唑嘌呤)治疗。使用一份协议表格记录pSS和NHL的主要特征。

结果

8例患者符合欧美共识标准(AECC)。pSS的主要表现为无痛性腮腺肿大(n = 7),其中6例为单侧;主要免疫特征为所有受检患者类风湿因子(RF)阳性和高免疫球蛋白血症(n = 7)。NHL的主要表现为脾肿大(n = 7)和淋巴结病(n = 5)。主要组织学亚型为黏膜相关淋巴组织(MALT)淋巴瘤(n = 4)和弥漫性大B细胞淋巴瘤(n = 2)。MALT淋巴瘤患者均无淋巴结原发性病变。8例患者有结外原发性病变,最常见于唾液腺(n = 4)和肺(n = 4)。

结论

pSS合并NHL患者的临床特征为无痛性单侧腮腺肿大、脾肿大、淋巴结病的发生率高,以高滴度RF和高免疫球蛋白血症为主的免疫模式,MALT淋巴瘤占优势,以及原发性结外受累频率升高。

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