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不同免疫状态患者肺毛霉病的临床特征

Clinical features of pulmonary mucormycosis in patients with different immune status.

作者信息

Peng Min, Meng Hua, Sun Yinghao, Xiao Yu, Zhang Hong, Lv Ke, Cai Baiqiang

机构信息

Division of Pulmonary and Critical Care Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.

Department of Ultrasound, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.

出版信息

J Thorac Dis. 2019 Dec;11(12):5042-5052. doi: 10.21037/jtd.2019.12.53.

Abstract

BACKGROUND

Pulmonary mucormycosis (PM) is a relatively rare but often fatal and rapidly progressive disease. Most studies of PM are case reports or case series with limited numbers of patients, and focus on immunocompromised patients. We investigated the clinical manifestations, imaging features, treatment, and outcomes of patients with PM with a focus on the difference in clinical manifestations between patients with different immune status.

METHODS

Clinical records, laboratory results, and computed tomography scans of 24 patients with proven or probable PM from January 2005 to December 2018 in Peking Union Medical College Hospital were retrospectively analyzed.

RESULTS

Ten female and 14 male patients were included (median age, 43.5 years; range, 13-64 years). Common presenting symptoms were fever (70.8%), cough (70.8%), sputum production (54.2%), and hemoptysis (41.7%). Radiological findings included consolidation (83.3%), ground-glass opacities (58.3%), nodules (50.0%), masses (37.5%), cavities (33.3%), mediastinal lymphadenopathy (29.2%), and halo sign (12.5%); one patient had a reversed halo sign. Seven patients (29.2%) had no obvious predisposing risk factors, and 17 (70.8%) had underlying diseases including diabetes, hematological malignancy, and use of immunosuppressants. Compared with immunocompromised patients, immunocompetent patients with PM were younger {23 [13-46] 48 [17-64] years, P=0.023}, comprised a higher proportion of men (100.0% 41.2%, P=0.019), had a longer disease course {34 [8-47] 9 [2-102] weeks, P=0.033}, had a higher eosinophil count [0.66 (0.07-2.00) ×10/L 0.04 (0.00-0.23) ×10/L, P=0.001], and had a lower erythrocyte sedimentation rate {12 [1-88] 74 [9-140] mm/h, P=0.032}.

CONCLUSIONS

PM can occur in heterogeneous patients with different immune status, and the clinical phenotype differs between immunocompetent and immunocompromised patients. Because of the lack of specific clinic and imaging manifestations, aggressive performance of invasive procedures to obtain histopathological and microbial evidence is crucial for a definitive diagnosis.

摘要

背景

肺毛霉病(PM)是一种相对罕见但通常致命且进展迅速的疾病。大多数关于PM的研究是病例报告或病例系列,患者数量有限,且主要关注免疫功能低下的患者。我们调查了PM患者的临床表现、影像学特征、治疗及预后,重点关注不同免疫状态患者的临床表现差异。

方法

回顾性分析了2005年1月至2018年12月在北京协和医院确诊或疑似PM的24例患者的临床记录、实验室检查结果及计算机断层扫描。

结果

纳入10例女性和14例男性患者(中位年龄43.5岁;范围13 - 64岁)。常见的首发症状为发热(70.8%)、咳嗽(70.8%)、咳痰(54.2%)及咯血(41.7%)。影像学表现包括实变(83.3%)、磨玻璃影(58.3%)、结节(50.0%)、肿块(37.5%)、空洞(33.3%)、纵隔淋巴结肿大(29.2%)及晕征(12.5%);1例患者有反晕征。7例患者(29.2%)无明显易感危险因素,17例(70.8%)有基础疾病,包括糖尿病、血液系统恶性肿瘤及使用免疫抑制剂。与免疫功能低下患者相比,免疫功能正常的PM患者更年轻{23 [13 - 46]对48 [17 - 64]岁,P = 0.023},男性比例更高(100.0%对41.2%,P = 0.019),病程更长{34 [8 - 47]对9 [2 - 102]周,P = 0.033},嗜酸性粒细胞计数更高[0.66(0.07 - 2.00)×10⁹/L对0.04(0.00 - 0.23)×10⁹/L,P = 0.001],红细胞沉降率更低{12 [1 - 88]对74 [9 - 140] mm/h,P = 0.032}。

结论

PM可发生于免疫状态不同的异质性患者中,免疫功能正常和免疫功能低下患者的临床表型不同。由于缺乏特异性的临床和影像学表现,积极进行侵入性操作以获取组织病理学和微生物学证据对于明确诊断至关重要。

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