一个被诊断为急性HIV的人持续CPK升高的特殊病例:背后是什么?

IF 1.7 4区 医学 Q3 INFECTIOUS DISEASES
HIV Research & Clinical Practice Pub Date : 2025-12-01 Epub Date: 2025-07-16 DOI:10.1080/25787489.2025.2533735
Lucrezia Calandrino, Serena Marinello, Luca Dal Bello, Elena Pegoraro, Anna Ferrari, Federico Nalesso, Annamaria Cattelan, Maria Mazzitelli
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引用次数: 0

摘要

在一个人身上常见和罕见疾病的共存可能是一个诊断挑战。我们在此报告的情况下,一个年轻的绅士诊断为急性艾滋病毒感染谁有肌痛和运动不耐受的历史,经历肌酐和磷酸激酶水平升高。临床表现:一名24岁的男性于2023年5月被诊断为急性HIV (HIV- rna bbb10 000 000拷贝/ml, CD4+计数417细胞/L),并于当天开始联合抗逆转录病毒治疗,使用达鲁那韦/可比司他/替诺福韦阿拉胺/恩曲他滨+多鲁替韦韦),6周后改用多鲁替韦/拉米夫定。5个月后,患者因发热、头痛、急性肾功能衰竭住院(肌酐500 umol/L)。随后,CPK达到峰值,达到22,000 mg/dl。他否认使用化学药物或药物,最近开始定期锻炼。HIV-RNA未检出,脑脊液检查无明显异常。随着实验室的正常化,cART暂时停止。20天后,随着症状复发需要再次住院,重新开始cART和身体活动。自身免疫和感染性检查均为阴性。疑似药物相关性肌炎(整合酶抑制剂作用下的肌病数据已报道),进行肌肉MRI,肌肉活检,遗传分析,毛发分析。他的可卡因和安非他明检测呈阳性。肌肉活检显示1型纤维萎缩,而肌肉磁共振成像无明显差异。2025年1月,基因检测结果证实为VII型糖原病。讨论:本病例突出了罕见代谢性疾病的诊断复杂性,特别是当与急性HIV、持续用药和药物暴露共存时。它使我们能够强调将罕见的代谢紊乱作为鉴别诊断的重要性,因为它们可以模拟全身性疾病或药物相关的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A peculiar case of persistent CPK elevation in a person diagnosed with acute HIV: what is behind?

Introduction: The coexistence of common and rare conditions in a single person may represent a diagnostic challenge. We herein report the case of a young gentleman diagnosed with an acute HIV infection who had a history of myalgias and exercise intolerance and experienced elevated creatinine and phosphokinase enzyme levels.

Clinical presentation: A 24-year-old gentleman was diagnosed with an acute HIV in May 2023 (HIV-RNA > 10.000.000 copies/ml, CD4+ count 417 cell/L) and started same-day combinarion antiretroviral therapy, cART, with darunavir/cobicistat/tenofovir alafenamide/emtricitabine+dolutegravir), switching to dolutegravir/lamivudine once undetectable, 6 weeks after. After 5 months, he was hospitalized with fever, headache, and acute renal failure (creatinine 500 umol/L). Later, CPK peaked at >22,000 mg/dl. He denied chemsex/drug use and had recently started exercising on a regular basis. HIV-RNA was undetectable, cerebrospinal fluid (CSF) examination was unremarkable. cART was temporarily stopped with the normalization of labs. After 20 days, cART was restarted, as well as physical activity, with relapse of the symptoms requiring rehospitalization. Workups for autoimmune and infectious causes were negative. Suspecting drug-related myositis (data on myopathies under integrase inhibitors have been reported), muscle MRI, muscle biopsy, genetic analyses, hair analysis were performed. He tested positive for cocaine and amphetamines. Muscle biopsy showed type 1 fiber atrophy while muscle magnetic resonance imaging was unremarkable. In January 2025, genetic testing came back confirming type VII glycogenosis.

Discussion: This case highlights the diagnostic complexity of rare metabolic disorders, especially when coexisting with acute HIV, continuous medication use and drug exposure. It allows us to highlight the importance of considering rare metabolic disorders as differential diagnoses, as they can mimic systemic illnesses or drug-related effects.

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CiteScore
2.90
自引率
6.20%
发文量
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