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首页> 外文期刊>Reumatologia >Is primary Sj?gren’s syndrome a risk factor for malignancies different from lymphomas? What does the literature highlight about it?
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Is primary Sj?gren’s syndrome a risk factor for malignancies different from lymphomas? What does the literature highlight about it?

机译:原发性干燥综合征是否不同于淋巴瘤是恶性肿瘤的危险因素?文献对此有何强调?

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Background : Primary Sj?gren’s syndrome (pSS) is a chronic systemic autoimmune disease with an elevated risk of developing lymphoproliferative malignancies (LM). Whether pSS is a risk factor or not for non-lymphoma malignancies (NLM) has been scarcely evaluated in the literature. Age is per se a risk factor for malignancies: patients over 70 years old have 4 times higher risk for cancers than adults. Even if the mean age of pSS onset usually is in the 4th and 5th decade, its onset in patients aged over 65 years (Elderly Onset pSS – EOpSS) is not uncommon. Material and methods : To evaluate pSS as a risk factor for NLM we performed a systematic electronic search on PubMed in the period 2006–2016 to identify all the publications on this topic. The studies were eligible for inclusion if they reported specific Standardized Incidence Ratio (SIR) with 95% CI. Studies that did not report sufficient published and/or original data were excluded. Results : Only 7 articles of 494 that we found in PubMed fulfilled the inclusion criterion. In the vast majority of these, SIR values were not statistically significant for NLM. The occurrence of NLM after LM was statistically significant in some studies and a NLM represented the most frequent cause of death. The possibility that NLM may represent a paraneoplastic syndrome seems much more frequent than LM, the risk of which increases with time after the diagnosis. Data regarding the neoplastic weight of EOpSS are mainly pointed out by case reports. Conclusions : Primary Sj?gren’s syndrome is not associated with an increased risk for NLM. However the possibility that NLM may appear after recovery from lymphoma should be carefully considered because it could be cause of the patient’s death. Similarly the possibility that NLM may represent a paraneoplastic syndrome must be highlighted. The relationship between EOpSS and SIRs for NLM should be deepened with studies on ad hoc cohorts.
机译:背景:原发性干燥综合征(pSS)是一种慢性全身性自身免疫性疾病,罹患淋巴增生性恶性肿瘤(LM)的风险较高。在文献中几乎没有评估过pSS是否是非淋巴瘤恶性肿瘤(NLM)的危险因素。年龄本身是恶性肿瘤的危险因素:70岁以上的患者患癌症的风险是成年人的4倍。即使pSS发作的平均年龄通常在第4和5十年,在65岁以上的患者中发作(老年发作pSS – EOpSS)也并不罕见。材料和方法:为了评估pSS作为NLM的危险因素,我们在2006-2016年期间对PubMed进行了系统的电子搜索,以识别有关该主题的所有出版物。如果研究报告特定的标准发病率(SIR)为95%CI,则符合纳入条件。没有报告足够的已发表和/或原始数据的研究被排除在外。结果:我们在PubMed中发现494篇文章中只有7篇符合纳入标准。在绝大多数情况下,SIR值对于NLM而言在统计上并不显着。在某些研究中,LM后发生NLM的发生在统计学上具有统计学意义,并且NLM代表最常见的死亡原因。 NLM代表副肿瘤综合征的可能性似乎比LM更为频繁,LM的风险随着诊断后的时间而增加。病例报告主要指出了有关EOpSS肿瘤重量的数据。结论:原发性干燥综合征与NLM风险增加无关。但是,应仔细考虑NLM从淋巴瘤恢复后可能出现的可能性,因为它可能导致患者死亡。同样,必须强调NLM可能代表副肿瘤综合征的可能性。 NLM的EOpSS和SIR之间的关系应通过专门队列研究来加深。

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