Suppr超能文献

西班牙安达卢西亚地区 127 例儿童内脏利什曼病继发噬血细胞性淋巴组织细胞增生症的实验室和临床特征:回顾性分析(2004-2019 年)

Distinct Laboratory and Clinical Features of Secondary Hemophagocytic Lymphohistiocytosis in Pediatric Visceral Leishmaniasis: A Retrospective Analysis of 127 Children in Andalusia, Spain (2004-2019).

机构信息

From the Unidad de Pediatría, Sección de Infectología, Reumatología e Inmunología Pediátrica, Hospital Infantil Virgen del Rocío, Instituto de Biomedicina de Sevilla, RITIP, Sevilla, Spain.

Unidad de Pediatría, Sección de Infectología Pediátrica, Hospital Universitario Reina Sofía, Córdoba, Spain.

出版信息

Pediatr Infect Dis J. 2021 Jun 1;40(6):525-530. doi: 10.1097/INF.0000000000003086.

Abstract

BACKGROUND

Visceral leishmaniasis (VL) is an endemic in Southern Europe. However, details regarding disease burden, clinical presentations, laboratory markers, management and outcome in children are scarce.

METHODS

Medical records of children (<14 years) admitted with VL to 10 pediatric units in Andalusia (2004-2019) were retrospectively reviewed. VL diagnosis was based on clinical presentation, serology, microscopy and molecular methods. Diagnosis of secondary hemophagocytic lymphohistiocytosis (sHLH) was established using the hemophagocytic lymphohistiocytosis-2004 criteria.

RESULTS

A total of 127 patients were identified. Median age was 14.5 months; the main clinical presentations were fever and splenomegaly (95.3% each). Cytopenias were the most common laboratory abnormalities. Diagnostics as well as treatment regimens varied over time and the participating centers. Liposomal amphotericin B was prescribed in 97.6%; relapses as well as adverse events were rarely observed (3.1% each). Thirty-seven patients, diagnosed with sHLH required longer hospital admission (P = 0.001), an increased number of platelet (P < 0.006) and red blood cell (P = 0.0001) transfusions and pediatric intensive care unit admission (P = 0.007). Monocytopenia (P = 0.011) and high C-reactive protein levels (P = 0.031), variables not included in the hemophagocytic lymphohistiocytosis-2004 criteria, were associated with sHLH. One patient deceased in the context of the Leishmania infection.

CONCLUSIONS

We report data on the largest pediatric VL cohort from Europe, commonly associated with sHLH. Raised C-reactive protein levels and monocytopenia appear to be associated with sHLH. The latter may help to identify these patients and to guide decisions regarding need of additional supportive clinical care and immunomodulatory therapies. The observed high rate of heterogeneity in terms of diagnosis and management warrants the establishment of appropriate guidelines.

摘要

背景

内脏利什曼病(VL)在南欧流行。然而,有关疾病负担、临床表现、实验室标志物、治疗和儿童结局的详细信息很少。

方法

回顾性分析了 2004 年至 2019 年安大路西亚 10 个儿科单位收治的 127 例儿童(<14 岁)的 VL 病历。VL 诊断基于临床表现、血清学、显微镜检查和分子方法。采用噬血细胞性淋巴组织细胞增生症-2004 标准诊断继发性噬血细胞性淋巴组织细胞增生症(sHLH)。

结果

共发现 127 例患者。中位年龄为 14.5 个月;主要临床表现为发热和脾肿大(各占 95.3%)。血细胞减少是最常见的实验室异常。诊断和治疗方案随时间和参与中心而变化。97.6%的患者使用了脂质体两性霉素 B;复发和不良事件很少见(各占 3.1%)。37 例诊断为 sHLH 的患者需要更长的住院时间(P=0.001)、更多的血小板(P<0.006)和红细胞(P=0.0001)输注以及儿科重症监护病房入院(P=0.007)。单核细胞减少症(P=0.011)和高 C 反应蛋白水平(P=0.031)与 sHLH 相关,这些变量未包含在噬血细胞性淋巴组织细胞增生症-2004 标准中。有 1 例患者死于利什曼原虫感染。

结论

我们报告了来自欧洲最大的儿科 VL 队列的数据,该队列通常与 sHLH 相关。C 反应蛋白水平升高和单核细胞减少症似乎与 sHLH 相关。后者可能有助于识别这些患者,并指导是否需要额外的支持性临床护理和免疫调节治疗的决策。观察到诊断和管理方面存在高度异质性,需要制定适当的指南。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验