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嗜肺军团菌作为急性血小板减少症的罕见病因:一例报告及文献综述

Legionella Pneumophila Presenting as a Rare Cause of Acute Thrombocytopenia: A Case Report and Review of Literature.

作者信息

Berenji Ryan, Faisal Sarah, Hussain Syed Ather, Faisal Asma, Faisal Hafsa

机构信息

General Physician Cancer Care, Williamsville, USA.

Jinnah Sindh Medical University, Karachi, Pakistan.

出版信息

Eur J Case Rep Intern Med. 2024 Aug 29;11(9):004817. doi: 10.12890/2024_004817. eCollection 2024.

Abstract

INTRODUCTION

can cause a wide spectrum of clinical manifestations, ranging from a mild flu-like illness to fulminant multi-organ involvement, characterised by severe pneumonia, diarrhoea, encephalopathy, shock, hepatic dysfunction and renal failure. Very rarely, it can be associated with haematologic conditions such as thrombotic thrombocytopenic purpura (TTP), haemolytic uraemic syndrome (HUS) and immune thrombocytopenic purpura (ITP). We report a rare case of causing ITP and review previously published cases of thrombocytopenia associated with Legionellosis in the literature.

CASE DESCRIPTION

A 53-year-old male presented with fevers, chills, a productive cough and severe haemoptysis. Blood work was remarkable for leukocytosis, severe thrombocytopenia and hyponatraemia. Computed tomography (CT) imaging showed left lower lobe lung consolidation, and a peripheral blood smear showed giant platelets consistent with ITP. Legionella urine antigen testing returned positive. He was treated with intravenous immunoglobin, steroid taper and a ten-day course of azithromycin, which led to normalisation of his platelet count and resolution of the pneumonia.

DISCUSSION

can lead to complement-mediated destruction of platelets resulting in ITP. Antibodies against can also cross-react with the enzyme ADAMTS13, inhibiting its function and resulting in TTP and HUS. Additionally, can infect vascular endothelial cells causing their death and stimulating release of von Willebrand factor (vWF) multimers into the bloodstream, promoting thrombosis and platelet consumption.

CONCLUSION

It is important for internists to consider in the differential for any patient presenting with pneumonia and severe thrombocytopenia. Earlier detection and intervention can lead to prevention of critical bleeding and better outcomes.

LEARNING POINTS

is rarely associated with different haematologic disorders resulting in severe bleeding diathesis as well as thrombosis.It is important for internists to consider in the differential diagnosis for any patient presenting with pneumonia and severe thrombocytopenia.Earlier detection and intervention can lead to prevention of critical bleeding and better outcomes.

摘要

引言

可引发广泛的临床表现,从轻微的流感样疾病到暴发性多器官受累,其特征为严重肺炎、腹泻、脑病、休克、肝功能障碍和肾衰竭。极少数情况下,它可与血栓性血小板减少性紫癜(TTP)、溶血性尿毒症综合征(HUS)和免疫性血小板减少性紫癜(ITP)等血液学疾病相关。我们报告一例罕见的导致ITP的病例,并回顾文献中先前发表的与军团病相关的血小板减少病例。

病例描述

一名53岁男性出现发热、寒战、咳痰和严重咯血。血液检查显示白细胞增多、严重血小板减少和低钠血症。计算机断层扫描(CT)成像显示左下叶肺实变,外周血涂片显示与ITP一致的巨大血小板。军团菌尿抗原检测呈阳性。他接受了静脉注射免疫球蛋白、逐渐减量的类固醇治疗以及为期十天的阿奇霉素疗程,这使他的血小板计数恢复正常且肺炎得到缓解。

讨论

可导致补体介导的血小板破坏,从而引发ITP。针对的抗体也可与酶ADAMTS13发生交叉反应,抑制其功能,进而导致TTP和HUS。此外,可感染血管内皮细胞,导致其死亡,并刺激血管性血友病因子(vWF)多聚体释放到血液中,促进血栓形成和血小板消耗。

结论

对于任何出现肺炎和严重血小板减少的患者,内科医生在鉴别诊断时考虑是很重要的。早期检测和干预可预防严重出血并带来更好的结果。

学习要点

很少与导致严重出血素质以及血栓形成的不同血液学疾病相关。对于任何出现肺炎和严重血小板减少的患者,内科医生在鉴别诊断时考虑是很重要的。早期检测和干预可预防严重出血并带来更好的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4020/11379109/3c18b638eb6b/4817_Fig1.jpg

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