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合并侵袭性肺曲霉病的重症发热伴血小板减少综合征致死病例的临床特征

Clinical features of fatal severe fever with thrombocytopenia syndrome that is complicated by invasive pulmonary aspergillosis.

作者信息

Chen Xiancheng, Yu Zhuxi, Qian Yajun, Dong Danjiang, Hao Yingying, Liu Ning, Gu Qin

机构信息

Department of Critical Care Medicine, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, No. 321 Zhongshan Road, Nanjing, Jiangsu Province, China.

Department of Critical Care Medicine, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, No. 321 Zhongshan Road, Nanjing, Jiangsu Province, China.

出版信息

J Infect Chemother. 2018 Jun;24(6):422-427. doi: 10.1016/j.jiac.2018.01.005. Epub 2018 Feb 7.

Abstract

INTRODUCTION

Severe fever with thrombocytopenia syndrome (SFTS) has been prevalent in parts of Asia during recent years. However, SFTS with invasive pulmonary aspergillosis (IPA) is rare, and it is important to understand its clinical features.

MATERIALS AND METHODS

Total four cases of SFTS with IPA are reviewed and detailing the disease progression, treatment options, and prognosis were summarized and analyzed.

RESULTS

The patients with SFTS-associated IPA first presented with fever, gastrointestinal symptoms, thrombocytopenia, leukopenia, and multiple organ failure. After 1-2 weeks, the patients developed mild polypnea and wheezing rales, and quickly developed dyspnea and respiratory failure. Tracheal intubation was usually performed, but did not relieve the intractable airway spasm and pulmonary ventilation failure. Bronchoscopy confirmed that the antifungal treatment was ineffective and the aspergillosis had worsened. All patients died of type 2 respiratory failure caused by continued airway obstruction and spasticity.

CONCLUSIONS

Given the high mortality rate in this series, there is a need for increased awareness of SFTS-associated IPA. Additional examinations should be performed in these cases, and early-stage antifungal treatment with organ support may be helpful.

摘要

引言

近年来,严重发热伴血小板减少综合征(SFTS)在亚洲部分地区流行。然而,合并侵袭性肺曲霉病(IPA)的SFTS较为罕见,了解其临床特征很重要。

材料与方法

回顾了4例合并IPA的SFTS病例,并总结分析了疾病进展、治疗选择及预后情况。

结果

合并IPA的SFTS患者最初表现为发热、胃肠道症状、血小板减少、白细胞减少及多器官功能衰竭。1至2周后,患者出现轻度气促和哮鸣音,随后迅速发展为呼吸困难和呼吸衰竭。通常进行气管插管,但无法缓解难治性气道痉挛和肺通气衰竭。支气管镜检查证实抗真菌治疗无效且曲霉病恶化。所有患者均死于持续性气道阻塞和痉挛导致的Ⅱ型呼吸衰竭。

结论

鉴于本系列病例的高死亡率,有必要提高对合并IPA的SFTS的认识。对此类病例应进行额外检查,早期抗真菌治疗及器官支持可能会有所帮助。

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