Case Report: When muscle edema is not a myositis flare: Legionella pneumonia complicated by rhabdomyolysis and acute kidney injury in long-standing polymyositis.

IF 3.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Frontiers in Medicine Pub Date : 2026-10-05 eCollection Date: 2026-01-01 DOI:10.3389/fmed.2026.1952498
Jing Zhang, Lina Zhang, Sheng-Guang Li, Yadan Zou, Ting Long, Ruohan Yu, Yanfeng Zhang, Ji Li
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引用次数: 0

Abstract

Legionella pneumophila is an important cause of severe community-acquired pneumonia and can produce extrapulmonary manifestations that obscure the primary diagnosis. Diagnostic error is especially likely in patients with established idiopathic inflammatory myopathy, because fever, myalgia, weakness, creatine kinase elevation and muscle edema may be attributed to autoimmune flare. We report a 70-year-old woman with a 25-year history of polymyositis receiving long-term corticosteroids and azathioprine who developed high fever, severe bilateral thigh pain and progressive proximal weakness after recent travel. On transfer, she had anuria with bladder distension, dark urine, diffuse posterior-thigh muscle edema, pneumonia, hyponatremia, metabolic acidosis, myoglobinemia and acute kidney injury. Legionella pneumonia with rhabdomyolysis and multifactorial acute kidney injury was suspected clinically, and Legionella-active antimicrobial therapy, hydration, urinary drainage and urine alkalinization were started before microbiological confirmation. A targeted sequencing-based respiratory pathogen assay on sputum collected on Day +4 detected L. pneumophila (145 sequences; estimated concentration <10^3 copies/mL) and respiratory syncytial virus A (266,036 sequences; 10^5 copies/mL), raising the possibility of viral-bacterial coinfection. Legionella urinary antigen, targeted PCR and culture were not documented. After infection and renal injury stabilized, methylprednisolone and intravenous immunoglobulin were used because residual inflammatory myopathy activity remained in the differential. However, creatine kinase and myoglobin had already declined, so subsequent improvement cannot be attributed specifically to immunomodulation. Creatinine fell from 538 μmol/L on Day 0 to 110 μmol/L on Day +9 and 78 μmol/L on Day +30; follow-up chest CT on Day +14 showed marked improvement. This case shows that muscle MRI edema is contextual rather than etiologic. In immunosuppressed myositis patients, pneumonia plus hyponatremia, myoglobinuria and renal injury should prompt early Legionella-active treatment while autoimmune activity is reassessed after infection control.

病例报告:当肌肉水肿不是肌炎爆发:军团菌肺炎合并横纹肌溶解和急性肾损伤长期多发性肌炎。
嗜肺军团菌是严重社区获得性肺炎的重要病因,可产生肺外表现,使初步诊断模糊不清。确诊为特发性炎症性肌病的患者尤其容易出现诊断错误,因为发热、肌痛、虚弱、肌酸激酶升高和肌肉水肿可能归因于自身免疫耀斑。我们报告了一位70岁的女性,患有25年的多发性肌炎病史,长期服用皮质类固醇和硫唑嘌呤,她在最近的旅行后出现高烧,严重的双侧大腿疼痛和进行性近端无力。转移时无尿伴膀胱膨胀、尿色深、弥漫性大腿后肌水肿、肺炎、低钠血症、代谢性酸中毒、肌红蛋白血症和急性肾损伤。临床怀疑为军团菌肺炎合并横纹肌溶解合并多因素急性肾损伤,在微生物学证实前开始军团菌活性抗菌治疗、水合、尿引流、尿碱化。对第4天采集的痰液进行基于靶向测序的呼吸道病原体检测,检测到嗜肺乳杆菌(145个序列);军团菌尿抗原估计浓度、靶向PCR和培养均未记录。在感染和肾损伤稳定后,由于炎性肌病的残余活动仍然存在,因此使用甲基强的松龙和静脉注射免疫球蛋白。然而,肌酸激酶和肌红蛋白已经下降,因此随后的改善不能特别归因于免疫调节。肌酐从第0天的538 μmol/L下降到第9天的110 μmol/L,第30天的78 μmol/L;随访第14天胸部CT显示明显好转。本病例显示肌肉MRI水肿是环境性的,而不是病因性的。在免疫抑制性肌炎患者中,肺炎合并低钠血症、肌红蛋白尿和肾损伤应提示早期积极治疗军团菌,同时在感染控制后重新评估自身免疫活性。
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来源期刊
Frontiers in Medicine
Frontiers in Medicine Medicine-General Medicine
CiteScore
5.10
自引率
5.10%
发文量
3710
审稿时长
12 weeks
期刊介绍: Frontiers in Medicine publishes rigorously peer-reviewed research linking basic research to clinical practice and patient care, as well as translating scientific advances into new therapies and diagnostic tools. Led by an outstanding Editorial Board of international experts, this multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. In addition to papers that provide a link between basic research and clinical practice, a particular emphasis is given to studies that are directly relevant to patient care. In this spirit, the journal publishes the latest research results and medical knowledge that facilitate the translation of scientific advances into new therapies or diagnostic tools. The full listing of the Specialty Sections represented by Frontiers in Medicine is as listed below. As well as the established medical disciplines, Frontiers in Medicine is launching new sections that together will facilitate - the use of patient-reported outcomes under real world conditions - the exploitation of big data and the use of novel information and communication tools in the assessment of new medicines - the scientific bases for guidelines and decisions from regulatory authorities - access to medicinal products and medical devices worldwide - addressing the grand health challenges around the world
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