A clinical analysis of hemophagocytic syndrome secondary to autoimmune diseases.

IF 1.1 Q4 RHEUMATOLOGY Archives of rheumatology Pub Date : 2022-12-01 eCollection Date: 2023-09-01 DOI:10.46497/ArchRheumatol.2023.9728
Yang Liu, Qian Li, Yazhen Su, Guozhu Che, Ying Liu, Pengyan Qiao, Sumiao Liu, Ke Xu
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Abstract

Objectives: This study aimed to analyze the differences of etiologies and clinical features between patients with autoimmune-associated hemophagocytic syndrome (AAHS) and those with other underlying diseases of hemophagocytic syndrome (HPS).

Patients and methods: The retrospective study was performed with 130 HPS patients (70 males, 60 females; mean age: 50.4±18.1 years; range, 13 to 85 years) between January 1st, 2011, and April 1st, 2022. The patients fulfilled at least five of the eight criteria proposed by the Histiocytosis Society in 2004. The underlying diseases related to HPS were divided into four categories: autoimmune, infection, malignancy and idiopathic diseases. And the clinical manifestations, laboratory examinations, treatments, and prognosis were analyzed respectively.

Results: Nineteen (14.6%) patients had AAHS, 45 (34.6%) had infection-associated HPS, 57 (43.8%) had malignancy-associated HPS, and nine (6.9%) had idiopathic HPS. The most common symptoms of HPS were unremitting fever in 123 (94.6%) of 130 patients and splenomegaly in 92 (70.8%). All patients manifested a decline of at least two lineages of hematopoietic cells. The absolute values of T cells and B cells of AAHS were significantly higher than that of malignancy-associated HPS. The levels of soluble CD25 (interleukin-2 receptor) of AAHS were the lowest among all-cause HPS (p<0.05). The all-cause mortality rate of hospitalized patients with HPS was 46.2%. The patients with AAHS had a better prognosis compared to other etiologies (odds ratio [OR]=0.091, 95% confidence interval [CI]: 0.011-0.775, p=0.028). Epstein-Barr virus infection (OR=4.761, 95% CI: 1.619-14.004, p=0.005) and pulmonary involvement (OR=4.555 95% CI: 1.524-13.609, p=0.007) were independent predictors of poor outcome in HPS. Thrombocytopenia (OR=0.978, 95% CI: 0.968-0.999, p=0.040) had a boundary effect on prognosis.

Conclusion: Patients with HPS secondary to autoimmune disease have better outcomes compared to patients complicated with Epstein-Barr virus infection or pulmonary involvement.

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自身免疫性疾病继发吞噬血细胞综合征的临床分析。
目的:本研究旨在分析自身免疫相关性噬血细胞综合征(AAHS)患者与其他基础疾病的噬血细胞综合征(HPS)患者的病因及临床特征的差异。患者和方法:回顾性研究了130例HPS患者(男性70例,女性60例;平均年龄:50.4±18.1岁;从2011年1月1日到2022年4月1日。这些患者至少符合组织细胞增多症学会2004年提出的8项标准中的5项。将与HPS相关的基础疾病分为自身免疫性疾病、感染性疾病、恶性肿瘤和特发性疾病4类。并分别对临床表现、实验室检查、治疗及预后进行分析。结果:AAHS 19例(14.6%),感染相关HPS 45例(34.6%),恶性相关HPS 57例(43.8%),特发性HPS 9例(6.9%)。130例患者中最常见的症状是持续发热123例(94.6%),脾肿大92例(70.8%)。所有患者都表现出至少两种造血细胞谱系的下降。AAHS患者T细胞和B细胞的绝对值明显高于恶性相关HPS患者。AAHS的可溶性CD25(白细胞介素-2受体)水平在全因HPS中最低。结论:与合并eb病毒感染或肺部受累的患者相比,继发于自身免疫性疾病的HPS患者预后更好。
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