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首页> 外文期刊>AIDS >Reactive haemophagocytic syndrome in 58 HIV-1-infected patients: clinical features, underlying diseases and prognosis.
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Reactive haemophagocytic syndrome in 58 HIV-1-infected patients: clinical features, underlying diseases and prognosis.

机译:58例HIV-1感染患者的反应性噬血细胞综合征:临床特征,潜在疾病和预后。

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OBJECTIVE: To describe features of reactive haemophagocytic syndrome (RHS) in HIV-1-infected adult patients. To compare characteristics of patients with malignancy-associated RHS and infection-associated RHS. DESIGN AND SETTING: Retrospective study in three departments of Infectious Diseases/Internal Medicine at three French tertiary centres. PATIENTS AND METHODS: Medical charts of HIV-1-infected adult patients and RHS seen between January 2006 and December 2007 were reviewed. Demographic, clinical and laboratory data obtained at the time of RHS episode were compared between patients with malignancy-associated RHS and infection-associated RHS using non-parametric tests. The overall survival was assessed using the Kaplan-Meier method. RESULTS: Fifty-eight HIV-1-infected patients were diagnosed with RHS [certain RHS n = 43, possible RHS n = 15, median (range) age 42 (23-85) years, men 76%]. At time of RHS, the median duration of HIV infection was 4 (0-22) years and 57% received HAART. The median CD4 lymphocyte count was 91 (2-387)/microl and 35% of patients had a plasma HIV-1 RNA less than 50 copies/ml. Underlying haemopathy/malignancy (Hodgkin lymphoma n = 10) or infection (tuberculosis n = 9, cytomegalovirus infection n = 5) were evidenced for 31 and 23 patients, respectively. Patients with haemopathy/malignancy-associated RHS presented more frequently with splenomegaly (97 vs. 70%, P < 0.01), lower aspartate aminotransferase (36 vs. 84 UI/l, P < 0.01) and lactate dehydrogenase (530 vs. 911 UI/l, P < 0.01) levels and CD8 cell count (234 vs. 588/microl, P < 0.01). Eighteen (31%) patients died. The overall survival was not statistically different between the two groups (P = 0.68). CONCLUSION: In the HAART era, RHS is frequently associated with underlying haemopathy/malignancy, especially Hodgkin lymphoma. The prognosis remains poor but seems, however, better than in the pre-HAART era.
机译:目的:描述感染HIV-1的成年患者的反应性噬血细胞综合征(RHS)的特征。为了比较恶性肿瘤相关RHS和感染相关RHS患者的特征。设计与地点:在法国三个大专院校的三个传染病/内科部门进行回顾性研究。病人和方法:回顾了2006年1月至2007年12月间HIV-1感染的成年患者和RHS的病历。使用非参数测试比较了恶性肿瘤相关性RHS和感染相关性RHS患者在RHS发作时获得的人口统计学,临床和实验室数据。使用Kaplan-Meier方法评估总生存期。结果:58例感染HIV-1的患者被诊断为RHS [某些RHS n = 43,可能的RHS n = 15,中位(范围)年龄42(23-85)岁,男性76%]。在进行RHS时,HIV感染的中位持续时间为4(0-22)年,其中57%接受了HAART。平均CD4淋巴细胞计数为91(2-387)/微升,35%的患者血浆HIV-1 RNA低于50拷贝/毫升。分别有31名和23名患者发生了潜在的血液病/恶性肿瘤(霍奇金淋巴瘤n = 10)或感染(结核病n = 9,巨细胞病毒感染n = 5)。患有血液病/恶性肿瘤相关性RHS的患者更常出现脾肿大(97%vs. 70%,P <0.01),较低的天冬氨酸转氨酶(36 vs. 84 UI / l,P <0.01)和乳酸脱氢酶(530 vs. 911 UI) / l,P <0.01)水平和CD8细胞计数(234对588 / microl,P <0.01)。 18名(31%)患者死亡。两组的总生存期无统计学差异(P = 0.68)。结论:在HAART时代,RHS经常与潜在的血液病/恶性肿瘤有关,尤其是霍奇金淋巴瘤。预后仍然很差,但似乎比HAART之前的时期要好。

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