Departamento de Medicina Interna, Hospital Clínico Universitario, Complexo Hospitalario Universitario de Santiago de Compostela, A Coruña 15706, Spain; Departamento de Medicina, Facultad de Medicina, Universidad de Santiago de Compostela, Santiago de Compostela, A Coruña, Spain.
Thrombosis and Vasculitis Unit, Complexo Hospitalario Universitario de Vigo, Vigo, Pontevedra, Spain.
Semin Arthritis Rheum. 2017 Aug;47(1):46-52. doi: 10.1016/j.semarthrit.2017.01.011. Epub 2017 Jan 29.
To perform a systematic review of all cases of the association between Kikuchi's disease (KD) and systemic lupus erythematosus (SLE), and to ascertain the clinical and laboratory characteristics of this association (KD-SLE).
We conducted a systematic search of the scientific literature until 31 January 2016. For study purposes, only patients aged >14 years, with histologically proven KD, definite SLE and adequate clinical data were included. To compare KD-SLE against isolated KD and SLE, we selected 2 large series of patients with KD and 4 series of SLE patients.
The search found 158 adults with proven KD-SLE. Of these, 113 with sufficient clinical information were included; 86 were women (female:male ratio = 5.0); mean age at diagnosis was 34 years (range: 14-56 years); and an ethnic distribution of 50.5% Asian, 34% Caucasian, and 15% other. KD-SLE patients differed significantly from patients with isolated KD, presenting with a higher frequency of high fever (90%), severe KD (88%), and extranodal manifestations. When compared to patients with SLE, those with KD-SLE presented with a higher frequency of fever and systemic symptoms and a lower frequency of lupus nephritis (22%). SLE had been diagnosed before KD in 18% of cases, simultaneously in 51%, and after KD in 31%. No significant differences were found in terms of time of diagnosis.
While KD-SLE patients share many clinical and laboratory manifestations with SLE, they differ in a lower frequency of lupus nephritis. The relative time of diagnosis of each disease did not affect the clinical expression of KD-SLE.
对所有与菊池病(KD)和系统性红斑狼疮(SLE)相关的病例进行系统回顾,以确定这种关联(KD-SLE)的临床和实验室特征。
我们对科学文献进行了系统检索,截止日期为 2016 年 1 月 31 日。出于研究目的,仅纳入年龄>14 岁、组织学证实的 KD、明确的 SLE 和充足临床数据的患者。为了将 KD-SLE 与孤立性 KD 和 SLE 进行比较,我们选择了 2 个大型 KD 患者系列和 4 个 SLE 患者系列。
搜索发现 158 例成人 KD-SLE。其中,有 113 例具有足够的临床信息被纳入;86 例为女性(女:男比例=5.0);诊断时的平均年龄为 34 岁(范围:14-56 岁);种族分布为 50.5%亚洲人,34%白种人,15%其他。KD-SLE 患者与孤立性 KD 患者显著不同,表现为高热(90%)、严重 KD(88%)和结外表现的频率更高。与 SLE 患者相比,KD-SLE 患者发热和全身症状的频率更高,狼疮肾炎的频率更低(22%)。在 18%的病例中,SLE 在 KD 之前被诊断,在 51%的病例中同时被诊断,在 31%的病例中在 KD 之后被诊断。诊断时间上没有显著差异。
尽管 KD-SLE 患者与 SLE 有许多临床和实验室表现相似,但狼疮肾炎的频率较低。每种疾病的相对诊断时间并不影响 KD-SLE 的临床表现。