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首页> 外文期刊>Medicine. >Factors associated with underlying malignancy in a retrospective cohort of 121 patients with dermatomyositis.
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Factors associated with underlying malignancy in a retrospective cohort of 121 patients with dermatomyositis.

机译:回顾性研究121例皮肌炎患者的潜在恶性肿瘤相关因素。

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Demographic, clinical, and laboratory features that predict underlying malignancy in patients with dermatomyositis (DM) are poorly known. We conducted a retrospective study in all adult patients with a definite (n = 75) or probable (n = 32) diagnosis of DM according to Bohan and Peter criteria or with amyopathic DM (n = 14) who were referred to 2 departments during a 13-year period. The diagnosis of malignancy-associated DM was retained if DM occurred in a context of recently diagnosed malignancy or if a malignancy was diagnosed during the 5 years following the diagnosis of DM. The Kaplan-Meier method was used to assess the cumulative incidence rates of underlying malignancy during the first 5 years of DM. Factors associated with malignancy in patients with DM were identified by Cox proportional hazards models. During the study period, 121 patients fulfilled the inclusion criteria (median age, 52 yr; range, 19-77 yr; women: 70%). For 29 of them, the diagnosis of malignancy-associated DM was retained. The cumulative incidence rate of malignancy was 21 +/- 4% and 28 +/- 5%, 1 year and 5 years after the diagnosis of DM, respectively. The median duration of follow-up of the 92 patients with no malignancy diagnosed was 36 months (range, 1-140 mo). In multivariate analysis, independent factors associated with an underlying malignancy in patients with DM were an age at diagnosis >52 years (hazard ratio [HR], 7.24; 95% confidence interval [CI], 2.35-22.31), a rapid onset of skin and/or muscular symptoms (HR, 3.11; 95% CI, 1.07-9.02), the presence of skin necrosis (HR, 3.84; 95% CI, 1.00-14.85) or periungual erythema (HR, 3.93; 95% CI, 1.16-13.24), and a low baseline level of complement factor C4 (HR, 2.74; 95% CI, 1.11-6.75). Lastly, low baseline lymphocyte count (<1500/mm(3)) was a protective factor of malignancy (HR, 0.33; 95% CI, 0.14-0.80). Taken together, these data may help physicians focus on a group of patients who might benefit from extensive evaluation for malignancy.
机译:预测皮肌炎(DM)患者潜在恶性肿瘤的人口统计学,临床和实验室特征知之甚少。我们根据Bohan和Peter的标准对所有诊断为DM的确诊(n = 75)或可能(n = 32)或患有肌病性DM(n = 14)的成人患者进行了回顾性研究,这些患者在两次13年期限。如果在最近诊断为恶性肿瘤的情况下发生DM或在DM诊断后的5年内诊断出恶性肿瘤,则保留与恶性肿瘤相关的DM的诊断。 Kaplan-Meier方法用于评估DM最初5年内潜在恶性肿瘤的累积发生率。通过Cox比例风险模型确定与DM患者恶性肿瘤相关的因素。在研究期间,有121位患者符合纳入标准(中位年龄52岁;范围19-77岁;女性:70%)。其中29例保留了与恶性肿瘤相关的DM的诊断。 DM诊断后1年和5年,恶性肿瘤的累积发病率分别为21 +/- 4%和28 +/- 5%。被诊断为无恶性肿瘤的92例患者的中位随访时间为36个月(范围1-140 mo)。在多变量分析中,与DM患者潜在的恶性肿瘤相关的独立因素是诊断时的年龄> 52岁(危险比[HR],7.24; 95%置信区间[CI],2.35-22.31),皮肤快速发作和/或肌肉症状(HR,3.11; 95%CI,1.07-9.02),皮肤坏死(HR,3.84; 95%CI,1.00-14.85)或唇周红斑(HR,3.93; 95%CI,1.16) -13.24)和较低的补体因子C4基线水平(HR,2.74; 95%CI,1.11-6.75)。最后,低基线淋巴细胞计数(<1500 / mm(3))是恶性肿瘤的保护因素(HR,0.33; 95%CI,0.14-0.80)。综上所述,这些数据可以帮助医生将重点放在可能从恶性肿瘤的广泛评估中受益的一组患者上。

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