• 文章类型: Journal Article
    目前强迫症的心理治疗方法,虽然有效,有复杂的结果和混合的疗效。先前的研究已经观察到强迫症患者的基线脑激活模式,阐明这种疾病的一些含义。观察基于证据的精神疗法对强迫症脑激活的影响(通过MRI)可以提供更全面的病理学概述。这项系统评价和荟萃分析评估了认知行为疗法(CBT)与暴露反应预防(ERP)对强迫症患者脑激活的影响。系统地搜索了学术数据库,评估的结局包括基线和治疗后大脑激活和症状严重程度的变化.患者(n=193)已确认OCD诊断,并接受了由训练有素的治疗师提供的ERP计划的原型CBT。CBT与ERP计划的参与者表现出症状严重程度的显着改善(Cohen'sd=-1.91)。总的来说,CBT与ERP导致额叶治疗后活化降低(Cohen'sd=0.40),顶叶(科恩的d=0.79),时间(科恩的d=1.02),和枕叶(科恩的d=0.76),和小脑(科恩的d=-0.78)。研究结果支持CBT与ERP改善OCD患者脑激活异常的能力。通过识别提高激活水平的区域,心理治疗计划可能受益于功能特异性功能的增加,这些功能特异性功能可以改善治疗结果.
    Current psychotherapeutic treatments for OCD, while effective, have complex outcomes with mixed efficacy. Previous research has observed baseline brain activation patterns in OCD patients, elucidating some of the implications of this disorder. Observing the effects of evidence-based psychotherapeutics for OCD on brain activation (through MRI) may provide a more comprehensive outline of pathology. This systematic review and meta-analysis evaluated the effects of cognitive behavioural therapy (CBT) with exposure-response prevention (ERP) on brain activation in OCD patients. Academic databases were systematically searched, and the outcomes evaluated included changes in brain activation and symptom severity between baseline and post-treatment. Patients (n = 193) had confirmed OCD diagnosis and underwent protocolized CBT with ERP programs delivered by trained therapists. Participants in the CBT with ERP programs demonstrated significant improvements in symptom severity (Cohen\'s d = - 1.91). In general, CBT with ERP resulted in decreased activation post-treatment in the frontal (Cohen\'s d = 0.40), parietal (Cohen\'s d = 0.79), temporal (Cohen\'s d = 1.02), and occipital lobe (Cohen\'s d = 0.76), and cerebellum (Cohen\'s d = - 0.78). The findings support CBT with ERP\'s ability to improve brain activation abnormalities in OCD patients. By identifying regions that improved activation levels, psychotherapy programs may benefit from the addition of function-specific features that could improve treatment outcomes.
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  • 文章类型: Journal Article
    快速眼动睡眠行为障碍(RBD)的神经影像学研究可以提供有关帕金森病(PD)发病机理的基本问题。跨模式,功能磁共振成像(fMRI)可能更适合识别路易体疾病早期阶段的神经网络之间的变化,当结构变化可能是微妙的或不存在时。这篇综述综合了RBD的所有fMRI研究结果,以进一步了解路易体疾病的病理生理学和进展。根据PRISMA指南在2000年1月至2024年2月之间进行的系统评价,确定了总共32项研究,用于孤立性RBD(iRBD)或继发于PD的RBD患者的原始fMRI研究。与健康对照相比,iRBD患者在脑干核中可检测到常见的功能改变,基底神经节,额叶和枕叶,和整个大脑网络测量。已确诊的PD和RBD患者表现出整个大脑和脑干核的功能连接下降,但与没有RBD的PD患者相比,小脑和额叶的功能连接增加。最后,静息状态功能连接的纵向变化与疾病进展有关.目前,RBD中的fMRI研究已经证明了运动和非运动途径中神经变性的早期特征。虽然需要更多的工作,这些发现有可能让我们了解疾病,有助于区分前驱PD和路易体前驱痴呆,并支持在未来的疾病改良试验中开发基于功能磁共振成像的表型转化和进展结局指标。©2024作者(S)。由WileyPeriodicalsLLC代表国际帕金森症和运动障碍协会出版的运动障碍。
    Neuroimaging studies in rapid eye movement sleep behavior disorder (RBD) can inform fundamental questions about the pathogenesis of Parkinson\'s disease (PD). Across modalities, functional magnetic resonance imaging (fMRI) may be better suited to identify changes between neural networks in the earliest stages of Lewy body diseases when structural changes may be subtle or absent. This review synthesizes the findings from all fMRI studies of RBD to gain further insight into the pathophysiology and progression of Lewy body diseases. A total of 32 studies were identified using a systematic review conducted according to PRISMA guidelines between January 2000 to February 2024 for original fMRI studies in patients with either isolated RBD (iRBD) or RBD secondary to PD. Common functional alterations were detectable in iRBD patients compared with healthy controls across brainstem nuclei, basal ganglia, frontal and occipital lobes, and whole brain network measures. Patients with established PD and RBD demonstrated decreased functional connectivity across the whole brain and brainstem nuclei, but increased functional connectivity in the cerebellum and frontal lobe compared with those PD patients without RBD. Finally, longitudinal changes in resting state functional connectivity were found to track with disease progression. Currently, fMRI studies in RBD have demonstrated early signatures of neurodegeneration across both motor and non-motor pathways. Although more work is needed, such findings have the potential to inform our understanding of disease, help to distinguish between prodromal PD and prodromal dementia with Lewy bodies, and support the development of fMRI-based outcome measures of phenoconversion and progression in future disease modifying trials. © 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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  • 文章类型: Case Reports
    浆液性囊性肿瘤是一种罕见的实体,具有良性病程。其成像特点,例如存在多个囊肿,有或没有结节状增强,可以模拟胰腺的其他囊性或实性病变。在计算机断层扫描(CT)或磁共振成像(MRI)上识别具有点状钙化的增强疤痕可能是提示这种诊断的独特发现。胰腺的神经内分泌肿瘤是不同的并且也是罕见的实体。在图像中,他们有早期动脉增强。在核磁共振中,它们在T2上是高强度的,在T1上是低强度的,具有强烈的对比度增强。介绍了一例胰腺有两个局灶性病变的患者,以及整合临床表现的重要性,诊断图像中的符号学,如果适用,说明了胰腺肿瘤最佳管理的组织病理学结果,强调放射科医师在这一过程中的关键作用。
    A serous cystic tumor is a rare entity that has a benign course. Its imaging characteristics, such as the presence of multiple cysts with or without nodular enhancement, can simulate other cystic or solid lesions of the pancreas. Identification of the enhancing scar with punctate calcifications on computed tomography (CT) or magnetic resonance imaging (MRI) may be a distinctive finding suggesting this diagnosis. Neuroendocrine tumors of the pancreas are a different and also rare entity. In images, they have early arterial enhancement. In MRI, they are hyperintense on T2 and hypointense on T1, with avid contrast enhancement. A case of a patient with two focal lesions in the pancreas is presented and the importance of integrating clinical findings, semiology in diagnostic images and, if applicable, the histopathological result for the optimal management of pancreatic tumors is illustrated, highlighting the crucial role of a radiologist in this process.
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  • 文章类型: Case Reports
    我们报告了一例通过腹外缝合进行初次闭合修复的Morgagni疝。此外,我们回顾了腹腔镜修复的Morgagni疝病例,已知疝气缺损的大小,建立网格利用率的尺寸标准。一名87岁的妇女因右上腹部疼痛和呕吐来到我们医院。她没有腹部手术或外伤史。胸部X线摄影和计算机断层扫描(CT)显示Morgagni疝,胃和横结肠突出进入右胸腔。最初,由于她的年龄,对胃疝进行了内窥镜修复,这是成功的。然而,两天后她复发了,促使我们进行半紧急腹腔镜手术。腹腔镜检查显示有Morgagni缺陷,用网膜,横结肠,胃突出,胃因气腹而缩小。幸运的是,突出的器官可以很容易地重新定位到腹部,没有粘连。疝缺损测量为6x3厘米。我们用腹外缝合进行了初次闭合。未进行囊切除。手术持续98分钟。术后第1天开始口服,患者于术后第3天出院,无并发症。术后1个月胸部X线和CT扫描显示无复发,在9个月的随访检查中,患者仍无症状。根据我们的审查结果,原发性闭合是治疗小疝缺损的有效方法(经验法则:宽度,<4厘米;长度,<7厘米)。
    We report a case of a Morgagni hernia repaired by primary closure with an extra-abdominal suture. Moreover, we reviewed cases of laparoscopically repaired Morgagni hernia, in which the size of the hernia defect was known, to establish a size criterion for mesh utilization. An 87-year-old woman presented to our hospital with right upper abdominal pain and vomiting. She had no history of abdominal surgery or trauma. Chest radiography and computed tomography (CT) revealed a Morgagni hernia, with the stomach and transverse colon herniated into the right chest cavity. Initially, an endoscopic repair was performed for the herniated stomach due to her age, which was successful. However, she had a recurrence 2 days later, prompting us to perform a semi-emergent laparoscopic surgery. Laparoscopic examination revealed a Morgagni defect, with the omentum, transverse colon, and stomach herniated, with the stomach reduced by pneumoperitoneum. Fortunately, the herniated organs could be easily relocated into the abdomen with no adhesions. The hernia defect measured 6 x 3 cm. We performed primary closure with an extra-abdominal suture. No sac resection was performed. The operation lasted 98 min. Oral intake was initiated on postoperative day 1, and the patient was discharged on postoperative day 3 without complications. Chest radiography and CT scans at 1 month postoperatively showed no recurrence, and the patient remained asymptomatic at the 9-month follow-up examination. According to our review findings, primary closure is an efficient method for small hernia defects (rule of thumb: width, <4 cm; length, <7 cm).
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  • 文章类型: Journal Article
    目的:本研究旨在通过系统评价,探讨使用绳肌腱(HT)自体前交叉韧带重建(ACLR)后髌股关节(PFJ)软骨损伤的发生。
    方法:在PubMed中进行了全面搜索,Embase,CochraneLibrary和GoogleScholar数据库查找从数据库开始到2023年11月15日发表的文章。搜索条件为[(\'前交叉韧带\'[网格]或\'前交叉韧带\'或\'ACL\')和\'重建\'和\'软骨\'和(\'二次看关节镜\'或\'二次看关节镜\'或\'MRI\'或\'磁共振成像\')]。纳入标准是报道使用HT自体移植物的ACLR后发生PFJ软骨损伤的研究,通过二次关节镜检查或随访磁共振成像(MRI)确定。
    结果:15项研究(1084例患者)符合纳入标准,随访期为1至5年。在第二次关节镜检查的结果中,观察到软骨等级恶化,髌骨的MDs范围为0.1至2.0,滑车的MDs范围为0至1.0。随访MRI结果报道PFJ软骨退变的发生率为20%至44%。患者报告的结果指标通常与PFJ软骨损伤没有显着关联。这篇综述中的研究报道了软骨损伤发展的各种危险因素。
    结论:PFJ软骨病变,使用二次关节镜或后续MRI检测到,经常在使用HT自体移植物的ACLR后不久发展。在这个阶段,患者可能不会表现出特定的症状;然而,有风险因素的患者需要临床医师在随访期间进行仔细观察和评估.
    方法:四级。
    OBJECTIVE: This study aimed to investigate the development of patellofemoral joint (PFJ) cartilage lesions following anterior cruciate ligament reconstruction (ACLR) using hamstring tendon (HT) autograft through a systematic review.
    METHODS: A comprehensive search was conducted in PubMed, Embase, Cochrane Library and Google Scholar databases to find articles published from database inception until 15 November 2023. The search terms were [(\'Anterior Cruciate Ligament\' [mesh] OR \'anterior cruciate ligament\' OR \'ACL\') AND \'reconstruction\' AND \'cartilage\' AND (\'second look arthroscopy\' OR \'second-look arthroscopy\' OR \'MRI\' OR \'magnetic resonance imaging\')]. Inclusion criteria were studies that reported on the occurrence of PFJ cartilage lesions following ACLR using HT autograft, as determined by second-look arthroscopy or follow-up magnetic resonance imaging (MRI).
    RESULTS: Fifteen studies (1084 patients) met the inclusion criteria, with follow-up periods ranging from 1 to 5 years. In the results of second-look arthroscopy, cartilage grade deterioration was observed, ranging from MDs of 0.1 to 2.0 in the patella and from 0 to 1.0 in the trochlea. Follow-up MRI results reported the incidence of PFJ cartilage degeneration with rates ranging from 20% to 44%. Patient-reported outcome measures often showed no significant association with PFJ cartilage lesions. The studies included in this review reported various risk factors for cartilage lesion development.
    CONCLUSIONS: Cartilage lesions in the PFJ, detected using second-look arthroscopy or follow-up MRI, frequently develop shortly after ACLR using HT autograft. At this stage, patients might not show specific symptoms; however, those with risk factors require careful observation and evaluation by clinicians during follow-up.
    METHODS: Level IV.
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  • 文章类型: English Abstract
    Automatic detection of pulmonary nodule based on computer tomography (CT) images can significantly improve the diagnosis and treatment of lung cancer. However, there is a lack of effective interactive tools to record the marked results of radiologists in real time and feed them back to the algorithm model for iterative optimization. This paper designed and developed an online interactive review system supporting the assisted diagnosis of lung nodules in CT images. Lung nodules were detected by the preset model and presented to doctors, who marked or corrected the lung nodules detected by the system with their professional knowledge, and then iteratively optimized the AI model with active learning strategy according to the marked results of radiologists to continuously improve the accuracy of the model. The subset 5-9 dataset of the lung nodule analysis 2016(LUNA16) was used for iteration experiments. The precision, F1-score and MioU indexes were steadily improved with the increase of the number of iterations, and the precision increased from 0.213 9 to 0.565 6. The results in this paper show that the system not only uses deep segmentation model to assist radiologists, but also optimizes the model by using radiologists\' feedback information to the maximum extent, iteratively improving the accuracy of the model and better assisting radiologists.
    基于电子计算机断层扫描(CT)影像的肺结节自动检测可以有效辅助肺癌诊治,但当前缺乏有效的交互工具将放射科医生的判读结果实时记录并反馈,以优化后台算法模型。本文设计并研发了一个支持CT图像肺结节辅助诊断的在线交互审查系统,通过预置模型检测出肺结节展示给医生,医生利用专业知识对检测的肺结节进行标注,然后根据标注结果采用主动学习策略对内置模型进行迭代优化,以持续提高模型的准确性。本文以开源肺结节数据集——肺结节分析2016(LUNA16)的5~9号子集进行迭代实验,随着迭代次数的增加,模型的准确率、调和分数和交并比指标稳定提升,准确率从0.213 9提高至0.565 6。本文研究结果表明,该系统能在使用深度分割模型辅助医生诊断的同时,最大程度地利用医生的反馈信息来优化模型,迭代提高模型的准确性,从而更好地辅助医生工作。.
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  • 文章类型: Journal Article
    类风湿性关节炎(RA)是由软骨关节炎症引起的系统性自身免疫性疾病,破坏关节和软骨,导致滑膜炎和血管推拉的形成。RA的及时发现和有效管理对于减轻炎症性关节炎的后果至关重要。可能影响疾病进展。使用放射性标记的靶向载体的核医学为RA诊断和对治疗评估的反应提供了有希望的途径。放射性药物,如99m(99mTc),结合单光子发射计算机断层扫描(SPECT)结合CT(SPECT/CT),引入了一种更精细的诊断方法,通过精确的解剖定位提高准确性,代表了用于RA评估的混合分子成像的显着进步。这篇综合综述讨论了现有的研究,包括体外,在体内,和临床研究探讨99mTc放射性标记靶向载体SPECT显像在RA诊断中的应用。本综述的目的是强调该策略通过改善RA的早期发现和管理来提高患者预后的潜力。
    Rheumatoid arthritis (RA) is a systemic autoimmune disorder caused by inflammation of cartilaginous diarthrodial joints that destroys joints and cartilage, resulting in synovitis and pannus formation. Timely detection and effective management of RA are pivotal for mitigating inflammatory arthritis consequences, potentially influencing disease progression. Nuclear medicine using radiolabeled targeted vectors presents a promising avenue for RA diagnosis and response to treatment assessment. Radiopharmaceutical such as technetium-99m (99mTc), combined with single photon emission computed tomography (SPECT) combined with CT (SPECT/CT), introduces a more refined diagnostic approach, enhancing accuracy through precise anatomical localization, representing a notable advancement in hybrid molecular imaging for RA evaluation. This comprehensive review discusses existing research, encompassing in vitro, in vivo, and clinical studies to explore the application of 99mTc radiolabeled targeting vectors with SPECT imaging for RA diagnosis. The purpose of this review is to highlight the potential of this strategy to enhance patient outcomes by improving the early detection and management of RA.
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  • 文章类型: Journal Article
    术语先天性肺畸形(CLM)用于描述具有不同影像学和临床表现的多种病理状况。这些异常源于胚胎肺发育异常,可能发生在产前生活的各个阶段。他们的自然史可以是可变的,呈现广泛的严重程度,包括一直持续到成年的无症状个体,以及那些在新生儿期经历呼吸窘迫的人。通过PubMed数据库,我们对先天性肺异常领域的文献进行了广泛的回顾,包括他们的诊断方法和发现。从我们的RIS-PACS数据库中,我们选择了最终诊断为先天性肺畸形的病例。选择了不同的诊断方法,包括使用X线平片研究的临床病例,CT扫描,产前超声检查,MR图像遇到最多的异常可以分为三类:支气管肺异常(先天性肺气道畸形(CPAM),先天性肺叶过度充气,支气管闭锁,和支气管囊肿),血管异常(动静脉畸形),以及合并的肺和血管异常(弯刀综合征和支气管肺隔离症)。CLM导致显著的发病率和死亡率;因此,认识到这些异常对于最佳的产前咨询和早期的产前和产后管理是必要的.本图片审查旨在报告相关的影像学发现,以便为放射科医生和儿科顾问提供一些鉴别诊断线索。
    The term congenital lung malformation (CLM) is used to describe a wide range of pathological conditions with different imaging and clinical manifestations. These anomalies stem from abnormal embryological lung development, potentially occurring across various stages of prenatal life. Their natural history can be variable, presenting in a wide range of severity levels and encompassing asymptomatic individuals who remain so until adulthood, as well as those who experience respiratory distress in the neonatal period. Through the PubMed database, we performed an extensive review of the literature in the fields of congenital lung abnormalities, including their diagnostic approach and findings. From our RIS-PACS database, we have selected cases with a final diagnosis of congenital lung malformation. Different diagnostic approaches have been selected, including clinical cases studied using plain radiograph, CT scan, prenatal ultrasound, and MR images. The most encountered anomalies can be classified into three categories: bronchopulmonary anomalies (congenital pulmonary airway malformations (CPAMs), congenital lobar hyperinflation, bronchial atresia, and bronchogenic cysts), vascular anomalies (arteriovenous malformation), and combined lung and vascular anomalies (scimitar syndrome and bronchopulmonary sequestration). CLM causes significant morbidity and mortality; therefore, the recognition of these abnormalities is necessary for optimal prenatal counseling and early peri- and postnatal management. This pictorial review aims to report relevant imaging findings in order to offer some clues for differential diagnosis both for radiologists and pediatric consultants.
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  • 文章类型: Journal Article
    经颅直流电刺激(tDCS)的神经生物学作用尚未明确阐明。一些研究表明,在额下回(IFG)上使用tDCS可以增强健康和神经系统个体的认知功能。在目标区域及其神经周围施加神经变化。在这次系统审查中,我们通过数据库搜索选择了健康和神经系成年人的随机假对照试验,以探索IFG上的tDCS结合认知训练是否调节功能连接或神经变化.最终纳入了20项研究,其中12项通过功能磁共振(fMRI)测量了TDCS效应,二通过功能近红外光谱(fNIRS),和六个通过脑电图(EEG)。由于在研究中观察到的高度异质性,对数据进行定性描述和比较以评估可靠性.总的来说,结合fMRI和tDCS的研究显示,局部和远处大脑区域的功能连接发生了广泛的变化。研究结果还表明,tDCS还可以调节目标区域下方的电生理变化。然而,这些结局并不总是伴随着相应的显著行为结果.这项工作提出了关于tDCS的一般功效的问题,其含义延伸到稳步增加的tDCS文献。
    The neurobiological effects of transcranial direct current stimulation (tDCS) have still not been unequivocally clarified. Some studies have suggested that the application of tDCS over the inferior frontal gyrus (IFG) enhances different aspects of cognition in healthy and neurological individuals, exerting neural changes over the target area and its neural surroundings. In this systematic review, randomized sham-controlled trials in healthy and neurological adults were selected through a database search to explore whether tDCS over the IFG combined with cognitive training modulates functional connectivity or neural changes. Twenty studies were finally included, among which twelve measured tDCS effects through functional magnetic resonance (fMRI), two through functional near-infrared spectroscopy (fNIRS), and six through electroencephalography (EEG). Due to the high heterogeneity observed across studies, data were qualitatively described and compared to assess reliability. Overall, studies that combined fMRI and tDCS showed widespread changes in functional connectivity at both local and distant brain regions. The findings also suggested that tDCS may also modulate electrophysiological changes underlying the targeted area. However, these outcomes were not always accompanied by corresponding significant behavioral results. This work raises the question concerning the general efficacy of tDCS, the implications of which extend to the steadily increasing tDCS literature.
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  • 文章类型: Case Reports
    背景:马拉色菌,属于担子菌群的亲脂性和脂肪依赖性酵母,是与各种皮肤疾病相关的机会性真菌病原体,包括脂溢性皮炎和头皮屑。通常,新生儿的马拉色菌感染表现为真菌血症或向骨或肺的血行播散。然而,由于非特异性临床表现和实验室/影像学发现,由这些真菌引起的椎体骨髓炎很少报道.病原体宏基因组学测序(PMseq)技术可以直接对感染标本进行高通量测序,通过全面的报告,促进临床样品中所有微生物的快速准确检测。
    方法:2022年7月20日,我院收治52岁男性,有3个月的门诊困难和局限性下腰痛病史。脊柱的磁共振成像(MRI)检查显示不规则的骨破坏影响L2,L3和L5椎体。此外,在L3和L5之间的椎间盘观察到低T1和高T2强度病变。根据影像学表现对结核性脊柱炎进行推定诊断,尽管所有分枝杆菌测试结果均为阴性。然而,患者在接受常规抗结核治疗3个月后未出现改善.随后的MRI显示椎体内存在扩张性异常信号,导致进行性骨骼破坏。通过来自L4椎体的血液和病理组织的培养证实不存在脊柱结核或其他感染性微生物。随后,对标本进行PMseq,揭示M.liquitta是相对丰度值最高的主要病原体。病理检查显示L4椎体中存在真菌菌丝体,周期性席夫亚甲基胺和高碘酸席夫氏染色呈阳性。抗结核治疗已停止,并给予氟康唑和伏立康唑的抗真菌组合。所有症状均在连续治疗7个月后缓解。病人能够自主走动。在13个月的随访期间,MRI显示椎体病变减少。
    结论:M.restricta不是与感染性椎体骨髓炎相关的常见病原体。然而,PMseq可以帮助诊断,及时治疗,以及一些非特异性传染病的决策。
    BACKGROUND: Malassezia restricta, a lipophilic and lipodependent yeast belonging to the basidiomycetes group, is an opportunistic fungal pathogen associated with various skin diseases, including seborrheic dermatitis and dandruff. Typically, Malassezia infection in neonates manifests as fungemia or hematogenous dissemination to the bone or lungs. However, vertebral osteomyelitis caused by these fungi is rarely reported owing to non-specific clinical presentations and laboratory/imaging findings. The Pathogen Metagenomics Sequencing (PMseq) technique enables direct high-throughput sequencing of infected specimens, facilitating the rapid and accurate detection of all microorganisms in clinical samples through comprehensive reports.
    METHODS: A 52-year-old male was admitted to our hospital on July 20, 2022 with a 3-month history of ambulatory difficulties and localized low back pain. Magnetic Resonance Imaging (MRI) examination of the spinal column revealed irregular bone destruction affecting the L2, L3, and L5 vertebral bodies. Additionally, low T1 and high T2 intensity lesions were observed at the intervertebral discs between L3 and L5. The presumptive diagnosis of tuberculous spondylitis was made based on the imaging findings, despite negative results in all mycobacterium tests. However, the patient exhibited no improvement after receiving regular anti-tuberculosis treatment for 3 months. Subsequent MRI revealed an expansive abnormal signal within the vertebral body, leading to progressive bone destruction. The absence of spinal tuberculosis or other infective microorganisms was confirmed through culture from blood and pathological tissue from the L4 vertebral body. Subsequently, PMseq was performed on the specimens, revealing M. restricta as the predominant pathogen with the highest relative abundance value. The pathological examination revealed the presence of fungal mycelium in the L4 vertebral body, with positive findings on periodic Schiff-methenamine and periodic acid-Schiff staining. The anti-tuberculosis treatment was discontinued, and an antifungal combination of fluconazole and voriconazole was administered. All symptoms were resolved after 7 consecutive months of treatment, and the patient was able to ambulate autonomously. Vertebral lesions were reduced on MRI during the 13-month follow-up.
    CONCLUSIONS: M. restricta is not a commonly recognized pathogen associated with infectious vertebral osteomyelitis. However, PMseq can aid in diagnosis, timely treatment, and decision making for some non-specific infectious diseases.
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