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Digging into uncertainty: a case report on Spitz lesions. 挖掘不确定因素:关于斯皮茨病变的病例报告。
IF 1.2 Q3 Medicine Pub Date : 2024-03-01
Eva Klara Merzel Šabović, Dragan Jejinić, Andreja Pagon, Nina Jugovar, Violeta Hosta

Spitz lesions represent a spectrum of melanocytic proliferations, and they include Spitz nevi, atypical Spitz tumors, and Spitz melanomas. Atypical Spitz tumors are intermediate melanocytic lesions with features between benign Spitz nevi and malignant Spitz melanomas. They often present a diagnostic challenge to pathologists and dermatologists alike because they can mimic melanoma, especially high-grade atypical Spitz tumors. Importantly, they present a relevant clinical management challenge because definite recommendations for their management and treatment have not yet been established. Here we present the case of a young patient with a high-grade atypical Spitz tumor along with the diagnostic procedure and further management. We also review potential pitfalls in the literature that should alert clinicians to the more aggressive potential of the lesion, such as some BRAF fusions.

斯皮茨病变是黑色素细胞增生的一种表现形式,包括斯皮茨痣、非典型斯皮茨瘤和斯皮茨黑色素瘤。非典型斯皮茨瘤是介于良性斯皮茨痣和恶性斯皮茨黑素瘤之间的黑素细胞病变。它们常常给病理学家和皮肤科医生带来诊断上的挑战,因为它们可以模拟黑色素瘤,尤其是高级别非典型斯皮茨瘤。重要的是,它们还带来了临床管理方面的挑战,因为对它们的管理和治疗还没有明确的建议。在此,我们将介绍一名患有高级别非典型斯皮茨肿瘤的年轻患者的病例,以及诊断过程和进一步的治疗方法。我们还回顾了文献中的潜在误区,这些误区应提醒临床医生注意该病变更具侵袭性的可能性,如某些 BRAF 融合。
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引用次数: 0
Review of virological methods for laboratory diagnosis and characterization of monkeypox virus (MPXV): lessons learned from the 2022 Mpox outbreak. 猴痘病毒(MPXV)实验室诊断和定性的病毒学方法回顾:从 2022 年猴痘爆发中吸取的经验教训。
IF 1.2 Q3 Medicine Pub Date : 2024-03-01
Katarina Resman Rus, Samo Zakotnik, Martin Sagadin, Marko Kolenc, Lucijan Skubic, Nataša Knap, Misa Korva, Mario Poljak, Tatjana Avšič-Županc

Monkeypox virus (MPXV), originally endemic in West Africa (Clade II) and Central Africa (Clade I), has recently emerged worldwide and has reinforced the need for rapid and accurate MPXV diagnostics. This review presents and critically discusses the range of virological methods for laboratory diagnosis and characterization of MPXV as well as related lessons learned and practical experience gained from the 2022 Mpox global outbreak. Real-time PCR is currently considered the diagnostic gold standard and ensures accurate and timely confirmation of suspected Mpox cases based on suspicious skin lesions, and digital PCR improves the precision of MPXV DNA quantification. Whole genome sequencing reveals the diversity within the Clade IIb outbreak and highlights the role of microevolution in the adaptation of the virus to the human host. Continuous genomic surveillance is important for better understanding of human-to-human transmission and prevention of the emergence of variola virus-like strains. Traditional virological methods such as electron microscopy and virus isolation remain essential for comprehensive virus characterization, particularly in the context of vaccine and antiviral drug development. Despite the current challenges, serological tests detecting a range of anti-MPXV antibodies are important adjunct diagnostic and research tools for confirmation of late-presenting or asymptomatic MPXV cases, contact tracing, epidemiological studies, seroepidemiological surveys, and better understanding of the role of IgG and neutralizing antibodies in the immune response to infection and vaccination. A multidisciplinary approach combining advanced molecular techniques with traditional virological methods is important for rapid and reliable diagnosis, surveillance, and control of the outbreak.

猴痘病毒(MPXV)最初流行于西非(第二支系)和中非(第一支系),最近在全球范围内出现,并加强了对快速准确的 MPXV 诊断的需求。本综述介绍并批判性地讨论了一系列用于 MPXV 实验室诊断和定性的病毒学方法,以及从 2022 年 Mpox 全球疫情中吸取的相关教训和实践经验。实时 PCR 目前被认为是诊断的黄金标准,可确保根据可疑皮损准确、及时地确诊疑似麻疹痘病例,而数字 PCR 则提高了 MPXV DNA 定量的精确度。全基因组测序揭示了支系 IIb 爆发的多样性,并强调了微进化在病毒适应人类宿主过程中的作用。持续的基因组监测对于更好地了解人与人之间的传播以及防止出现类似天花病毒的毒株非常重要。传统的病毒学方法,如电子显微镜和病毒分离,对于全面鉴定病毒特征仍然至关重要,尤其是在疫苗和抗病毒药物研发方面。尽管目前面临着各种挑战,但检测各种抗 MPXV 抗体的血清学检测仍是重要的辅助诊断和研究工具,可用于确诊晚期或无症状的 MPXV 病例、追踪接触者、流行病学研究、血清流行病学调查,以及更好地了解 IgG 和中和抗体在感染和接种疫苗的免疫反应中的作用。将先进的分子技术与传统的病毒学方法相结合的多学科方法对于快速可靠地诊断、监测和控制疫情非常重要。
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引用次数: 0
COVID-19 and oral lesions: 2020-2024 outpatient case series and literature review. COVID-19 与口腔病变:2020-2024 年门诊病例系列和文献综述。
IF 1.2 Q3 Medicine Pub Date : 2024-03-01
Ana Glavina, Jozo Badrov, Marino Lukenda, Karmela Džaja, Dolores Biočina-Lukenda, Liborija Lugović-Mihić

Data on oral lesions of coronavirus disease (COVID-19) are conflicting, and there are few evidence-based data on oral lesions directly caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The aim of this case series and literature review is to determine the prevalence of oral lesions associated with COVID-19 in outpatients and identify oral manifestations that are likely associated with COVID-19. We present 15 patients that came for their first specialist examination to the Oral Medicine Outpatient Clinic, Dental Clinic, Split, Croatia between November 2020 and January 2024. Their medical and dental history was taken following CARE guidelines. The prevalence of oral lesions associated with SARS-CoV-2 was 1.42% during the 4-year follow-up period. The most common oral lesions were nonspecific erosions, stomatitis, salivary flow disorders (xerostomia, oligosialia), salivary gland diseases (sialadenitis, chronic sialadenitis), candidiasis, pigmentation, aphthae, burning mouth syndrome, and geographic and fissured tongue. The mean latency period was 25.1 days. The site most commonly affected was the tongue (61.5%). Oral lesions associated with COVID-19 occurred in middle-aged patients, with an equal distribution by sex. They presented in a mild form and did not correlate with the severity of the clinical picture of COVID-19.

有关冠状病毒病(COVID-19)口腔病变的数据相互矛盾,而有关严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)直接引起的口腔病变的循证数据则很少。本病例系列和文献综述旨在确定门诊患者中与 COVID-19 相关的口腔病变的发病率,并识别可能与 COVID-19 相关的口腔表现。我们介绍了 2020 年 11 月至 2024 年 1 月期间到克罗地亚斯普利特牙科诊所口腔内科门诊进行首次专科检查的 15 名患者。他们的病史和牙科病史是按照 CARE 指南采集的。在 4 年的随访期间,与 SARS-CoV-2 相关的口腔病变发生率为 1.42%。最常见的口腔病变是非特异性糜烂、口腔炎、唾液流动障碍(口臭、少唾症)、唾液腺疾病(唾液腺炎、慢性唾液腺炎)、念珠菌病、色素沉着、蚜虫病、灼热口腔综合征以及地理舌和裂纹舌。平均潜伏期为 25.1 天。最常受影响的部位是舌头(61.5%)。与COVID-19相关的口腔病变多发于中年患者,男女比例相当。口腔病变的症状较轻,与COVID-19临床表现的严重程度无关。
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引用次数: 0
The relationship between sleep quality and chronotype differences and urticaria severity in patients with chronic spontaneous urticaria. 慢性自发性荨麻疹患者的睡眠质量和时间型差异与荨麻疹严重程度之间的关系。
IF 1.2 Q3 Medicine Pub Date : 2024-03-01
Gulhan Gurel, Dilara Guler, Hasan Ali Guler, İrem Nur Durusu Türkoğlu, Isın Nur Sultan Oncu, Seçil Soylu

Introduction: Chronic spontaneous urticaria (CSU) is characterized by persistent or recurrent pruritic lesions that last more than 6 weeks. Patients with CSU may experience sleep disturbances, particularly due to itching. Biological rhythms (chronotypes) are categorized as morningness, intermediate, and eveningness types. This study evaluates the relationship between sleep quality, chronotype, and disease severity in CSU patients.

Methods: The study included 53 CSU patients and 50 healthy controls. A sociodemographic data form was completed, and the disease severity was determined utilizing the Urticaria Activity Score over 7 days (UAS7). The Hospital Anxiety and Depression Scale (HADS), Insomnia Severity Index (ISI), and Pittsburgh Sleep Quality Index (PSQI) scales as well as the Morningness-Eveningness Scale (MEQ) were applied to the participants.

Results: The CSU group had a significantly higher body mass index (BMI) than that of the healthy control group. In terms of sleep and chronotype scales, compared to the control group, the CSU group had higher ISI scores as well as subscale scores on the PSQI subscales, with the exception of habitual sleep efficiency and total PSQI scores. There was no difference between MEQ scores. In the correlation analysis, the UAS7 and PSQI total scores were found to be correlated, whereas in the logistic regression analysis the estimated relative risk of BMI and PSQI total score for CSU was found to be 1.13 and 1.45, respectively.

Conclusions: When dealing with CSU patients, it is necessary to conduct a sleep quality assessment as part of a holistic evaluation.

简介慢性自发性荨麻疹(CSU)的特征是持续或反复出现瘙痒性皮损,且持续时间超过 6 周。慢性自发性荨麻疹患者可能会出现睡眠障碍,尤其是由于瘙痒引起的睡眠障碍。生物节律(时间型)可分为晨醒型、中间型和傍晚型。本研究评估了 CSU 患者的睡眠质量、时间型和疾病严重程度之间的关系:研究对象包括 53 名 CSU 患者和 50 名健康对照者。研究对象包括 53 名 CSU 患者和 50 名健康对照者,他们填写了一份社会人口学数据表,并通过 7 天荨麻疹活动评分(UAS7)确定了疾病的严重程度。研究人员还采用了医院焦虑和抑郁量表(HADS)、失眠严重程度指数(ISI)、匹兹堡睡眠质量指数(PSQI)量表以及晨间活力量表(MEQ):结果:CSU 组的体重指数(BMI)明显高于健康对照组。在睡眠和时间型量表方面,与对照组相比,CSU 组的 ISI 分数和 PSQI 分量表的子量表分数更高,但习惯性睡眠效率和 PSQI 总分除外。MEQ 分数之间没有差异。在相关性分析中,发现UAS7和PSQI总分具有相关性,而在逻辑回归分析中,发现BMI和PSQI总分对CSU的估计相对风险分别为1.13和1.45:结论:在处理 CSU 患者时,有必要将睡眠质量评估作为整体评估的一部分。
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引用次数: 0
Widespread dermatophytosis in a healthy adolescent: the first report of multidrug-resistant Trichophyton indotineae infection in the UAE. 一名健康青少年的大面积皮肤癣菌病:阿联酋首例耐多药毛癣菌感染病例。
IF 1.2 Q3 Medicine Pub Date : 2024-03-01
Miloš D Pavlović, Shireen Marzouk, Leis Bećiri

A multidrug-resistant dermatophyte species recently arose in India, first described as terbinafine-resistant Trichophyton interdigitale and soon given a separate name: T. indotineae. Thanks to its treatment recalcitrance, person-to-person spread, and frequent travel, before long it was identified in many countries on all continents. We describe here the case of a boy with widespread, extremely pruritic, inflammatory dermatophytosis affecting his face, neck, trunk, and extremities, unsuccessfully treated for months with oral terbinafine and fluconazole and a range of topical antimycotics. Qualitative polymerase chain reaction of skin scrapings from his lesions identified a T. interdigitale complex fungus, highly probably T. indotineae due to conspecificity and antifungal resistance. Oral itraconazole, administered over 8 weeks, cleared the infection. Because the patient had not traveled outside the United Arab Emirates for months before the infection became obvious, it must have been acquired from a local source.

印度最近出现了一种耐多种药物的皮癣菌,最初被描述为耐特比萘芬的Trichophyton interdigitale,不久又被单独命名为T. indotineae。由于其治疗顽固性、人与人之间的传播以及频繁的旅行,不久之后就在各大洲的许多国家发现了它。我们在此描述了一个男孩的病例,他患有广泛的、极度瘙痒的炎症性皮癣,面部、颈部、躯干和四肢都受到影响,口服特比萘芬、氟康唑和一系列外用抗霉菌药物治疗数月未果。对他皮损处的皮肤刮片进行定性聚合酶链式反应,发现了一种间位真菌复合菌,由于同种性和抗真菌耐药性,极有可能是吲哚替尼菌。口服伊曲康唑 8 周后,感染痊愈。由于患者在感染明显之前的几个月里没有到过阿拉伯联合酋长国以外的地方,因此感染肯定来自当地。
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引用次数: 0
Diagnostic accuracy of a short-form version of the diagnostic criteria for primary hyperhidrosis. 原发性多汗症诊断标准简表的诊断准确性。
IF 1.2 Q3 Medicine Pub Date : 2024-03-01
Mattias A S Henning, Hajer I Al-Rahimi, Gregor B E Jemec, Ole B Pedersen

Introduction: The gold standard method for diagnosing primary hyperhidrosis (PHH) is based on seven patient-reported criteria. By determining an individual criterion's diagnostic accuracy, one can identify short-version classification models.

Methods: In this cross-sectional study, data were collected from Danish blood donors in 2021. Cohen's kappa and diagnostic accuracy were determined by comparing each criterion with the gold standard method.

Results: The study included 1,039 participants. Of them, 59 (5.7%) had PHH and 980 (94.3%) were classified as control individuals. The PHH major criterion "focal visible excessive sweating for at least 6 months without an apparent cause" had the highest prevalence in the participants with PHH compared to the control individuals (100% vs. 0.6%; p < 0.0001). The agreement between this criterion and PHH was Cohen's kappa = 0.95 (95% confidence interval [CI] 0.91-0.99), and its sensitivity was 1.00 (95% CI 0.94-1.00) and specificity 0.99 (95% CI 0.99-1.00). The other criteria showed lower agreement and diagnostic accuracy.

Conclusions: The PHH major criterion showed near-perfect agreement and near-equal diagnostic accuracy compared with the gold standard method. This single criterion can be used as a short-form version to screen for PHH. Determination of reproducibility in independent populations is warranted.

导言:诊断原发性多汗症(PHH)的金标准方法基于七项患者报告标准。通过确定单个标准的诊断准确性,可以确定短版本分类模型:在这项横断面研究中,收集了 2021 年丹麦献血者的数据。方法:在这项横断面研究中,收集了 2021 年丹麦献血者的数据,通过将每项标准与金标准方法进行比较,确定了 Cohen's kappa 和诊断准确性:研究包括 1,039 名参与者。其中,59 人(5.7%)患有 PHH,980 人(94.3%)被列为对照组。与对照组相比,PHH 主要标准 "至少 6 个月无明显原因的局灶性明显多汗 "在 PHH 患者中的流行率最高(100% 对 0.6%;P < 0.0001)。该标准与 PHH 的一致性为 Cohen's kappa = 0.95(95% 置信区间 [CI] 0.91-0.99),灵敏度为 1.00(95% CI 0.94-1.00),特异性为 0.99(95% CI 0.99-1.00)。其他标准的一致性和诊断准确性较低:结论:与金标准方法相比,PHH 主要标准的一致性和诊断准确性接近完美。这一单一标准可作为筛查 PHH 的简易版本。有必要在独立人群中确定重现性。
{"title":"Diagnostic accuracy of a short-form version of the diagnostic criteria for primary hyperhidrosis.","authors":"Mattias A S Henning, Hajer I Al-Rahimi, Gregor B E Jemec, Ole B Pedersen","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Introduction: </strong>The gold standard method for diagnosing primary hyperhidrosis (PHH) is based on seven patient-reported criteria. By determining an individual criterion's diagnostic accuracy, one can identify short-version classification models.</p><p><strong>Methods: </strong>In this cross-sectional study, data were collected from Danish blood donors in 2021. Cohen's kappa and diagnostic accuracy were determined by comparing each criterion with the gold standard method.</p><p><strong>Results: </strong>The study included 1,039 participants. Of them, 59 (5.7%) had PHH and 980 (94.3%) were classified as control individuals. The PHH major criterion \"focal visible excessive sweating for at least 6 months without an apparent cause\" had the highest prevalence in the participants with PHH compared to the control individuals (100% vs. 0.6%; p < 0.0001). The agreement between this criterion and PHH was Cohen's kappa = 0.95 (95% confidence interval [CI] 0.91-0.99), and its sensitivity was 1.00 (95% CI 0.94-1.00) and specificity 0.99 (95% CI 0.99-1.00). The other criteria showed lower agreement and diagnostic accuracy.</p><p><strong>Conclusions: </strong>The PHH major criterion showed near-perfect agreement and near-equal diagnostic accuracy compared with the gold standard method. This single criterion can be used as a short-form version to screen for PHH. Determination of reproducibility in independent populations is warranted.</p>","PeriodicalId":45914,"journal":{"name":"Acta Dermatovenerologica Alpina Pannonica et Adriatica","volume":null,"pages":null},"PeriodicalIF":1.2,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140294934","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hereditary angioedema: do patients have a specific "digital fingerprint" in Danish registries? 遗传性血管性水肿:丹麦登记册中的患者有特定的 "数字指纹 "吗?
IF 1.2 Q3 Medicine Pub Date : 2024-03-01
Jakob Lillemoen Drivenes

Introduction: Hereditary angioedema (HAE) is a potentially life-threatening genetic disorder characterized by recurrent episodes of angioedema. From the onset of symptoms until diagnosis, patients often have several contacts with the healthcare system. It was hypothesized that a "digital fingerprint" of undiagnosed HAE patients could be identified in Danish registries.

Methods: This study compared patients with a control group of patients with a diagnosis of Quincke's edema (QE) or bee/wasp allergy because they could have phenotypic similarities.

Results: QE was the most common diagnosis code in the hospital sector among HAE patients before a specific diagnosis of HAE was established. HAE patients had been seen at the hospital on average once every other year before the diagnosis was established, and on average once during the year before the diagnosis was established. Many patients contacted a practicing dermatologist during the year before the diagnosis was established.

Conclusions: HAE patients had several hospital contacts due to swelling attacks during the years before their diagnosis was established, and half of them consulted a dermatologist. It was not possible to identify a specific "digital fingerprint" in Danish registries regarding specific procedures or diagnoses distinguishing them from the control group. It is therefore recommended that hospitalized patients with angioedema of unknown cause be screened for HAE.

简介:遗传性血管性水肿(HAE)是一种可能危及生命的遗传性疾病,其特点是血管性水肿反复发作。从出现症状到确诊,患者往往要与医疗系统进行多次接触。我们假设可以在丹麦登记册中找到未确诊 HAE 患者的 "数字指纹":本研究将患者与诊断为昆克氏水肿(QE)或蜂/蜂过敏的对照组患者进行了比较,因为它们可能具有表型相似性:结果:在确定HAE的具体诊断之前,QE是HAE患者在医院中最常见的诊断代码。在确诊前,HAE 患者平均每隔一年在医院就诊一次,在确诊前一年内平均就诊一次。许多患者在确诊前的一年中接触过执业皮肤科医生:结论:HAE患者在确诊前的数年内曾多次因肿胀发作而到医院就诊,其中半数患者曾咨询过皮肤科医生。在丹麦的登记册中,无法找到区别于对照组的特定程序或诊断的 "数字指纹"。建议对原因不明的血管性水肿住院患者进行HAE筛查。
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引用次数: 0
Clinical and immunopathological characteristics of autoimmune blistering skin diseases. 自身免疫性大疱性皮肤病的临床和免疫病理特征。
IF 1.2 Q3 Medicine Pub Date : 2023-12-01
Anita Gunarić, Dubravka Šimić, Branka Marinović

Autoimmune blistering skin diseases (AIBDs) encompass several heterogeneous conditions clinically characterized by blisters and erosions on the skin and mucous membranes and are immunopathologically characterized by autoantibodies against structural proteins of the skin. Those proteins are responsible for the intercellular contact between epidermal keratinocytes and adhesion of the basal keratinocytes to the dermis. Therefore, AIBDs are divided into two main groups: intraepidermal (the pemphigus group) and subepidermal (the pemphigoid) groups. The diagnostic methods for AIBDs have made tremendous progress in the last 2 decades due to the availability of standardized serological assays that allow precise diagnosis in most patients. If left untreated, these diseases are potentially life-threatening due to superinfections and loss of body fluids, and in some severe cases due to restricted food intake. Based on the available literature, this paper provides an overview of the clinical and immunopathological characteristics of the most common AIBDs.

自身免疫性水疱性皮肤病(AIBDs)包括几种临床上以皮肤和粘膜上的水疱和糜烂为特征的异质性疾病,其免疫病理特征是针对皮肤结构蛋白的自身抗体。这些蛋白质负责表皮角朊细胞之间的细胞间接触以及基底角朊细胞与真皮的粘附。因此,AIBD 主要分为两组:表皮内组(丘疹性荨麻疹组)和表皮下组(丘疹性荨麻疹组)。由于标准化血清学检测方法的出现,AIBD 的诊断方法在过去 20 年中取得了巨大进步,可以对大多数患者进行精确诊断。如果不及时治疗,这些疾病可能会因超级感染和体液流失而危及生命,在某些严重病例中还会因进食受限而危及生命。根据现有文献,本文概述了最常见的 AIBD 的临床和免疫病理特征。
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引用次数: 0
Efficacy of alitretinoin in the treatment of Darier disease: a case report. 阿利替诺治疗达里尔病的疗效:病例报告。
IF 1.2 Q3 Medicine Pub Date : 2023-12-01
Andreja Pagon, Mateja Dolenc Voljč

Darier disease is a rare autosomal dominant genodermatosis that initially first presents in adolescence with scaly reddish brown keratotic papules and plaques with a seborrheic and intertriginous distribution. The absence of specific targeted medications complicates the treatment process, and managing resistant cases can prove challenging due to recurrent exacerbations that may result in serious complications such as secondary bacterial and viral infections. Treatments of choice include antiseptics, topical corticosteroids, and systemic retinoids, mainly acitretin and isotretinoin. We report the case of a female patient with Darier disease that was unsuccessfully treated with acitretin and isotretinoin but showed significant improvement with alitretinoin. Previous reports on the efficacy of alitretinoin in Darier disease are reviewed.

达里尔病是一种罕见的常染色体显性遗传性皮肤病,最初在青春期发病,表现为鳞屑性红褐色角化性丘疹和斑块,皮脂溢出和皮损间分布。由于缺乏特定的靶向药物,治疗过程变得更加复杂,而且由于病情反复加重,可能导致继发性细菌和病毒感染等严重并发症,因此处理耐药病例可能具有挑战性。首选的治疗方法包括抗菌药、局部皮质类固醇激素和全身用维甲酸类药物,主要是阿曲汀和异维A酸。我们报告了一例女性达里尔病患者的病例,她曾接受过阿曲汀和异维A酸治疗,但效果不佳。本文回顾了以前关于阿利曲汀对达里尔病疗效的报道。
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引用次数: 0
New anti-aging strategies: a narrative review. 新的抗衰老战略:叙述性综述。
IF 1.2 Q3 Medicine Pub Date : 2023-12-01
Vana Stojić, Tea Štrbac, Andrija Stanimirović

The objective of anti-aging medicine is to decelerate the aging process and mitigate its associated effects, such as susceptibility to cancer, diabetes, and cardiovascular and neurodegenerative diseases. This review provides an overview of the latest advancements in this field, considering both pharmaceutical and non-pharmaceutical approaches. Electronic literature search involved three databases: MEDLINE, Cochrane, and Google Scholar, supplemented by other available literature. Strategies for delaying aging and related diseases comprise pharmaceutical interventions and lifestyle choices. It is crucial for these strategies to be substantiated by research-based evidence. Lifestyle options include fasting, fasting-mimicking, and ketogenic diets. Anti-aging drugs and supplements operate through diverse mechanisms. Calorie restriction mimetics include the activator of AMP-activated protein kinase (metformin) and inhibitor of mTOR (rapamycin), alongside rilmenidine, exhibiting both effects. Rosmarinic acid, a natural product, functions through its anti-glycation properties. Age-related protein crosslinks are acknowledged as a causative factor in age-related diseases. Anti-aging medicine is an evolving field with a multitude of drugs and strategies, necessitating further clinical studies and long-term follow-up based on clinical experience and insights gained from delayed adverse events.

抗衰老医学的目标是延缓衰老过程并减轻其相关影响,如癌症、糖尿病、心血管疾病和神经退行性疾病的易感性。本综述概述了这一领域的最新进展,同时考虑了药物和非药物方法。电子文献检索涉及三个数据库:MEDLINE、Cochrane 和 Google Scholar,并辅以其他可用文献。延缓衰老和相关疾病的策略包括药物干预和生活方式选择。这些策略必须有基于研究的证据支持。生活方式选择包括禁食、模拟禁食和生酮饮食。抗衰老药物和补充剂通过不同的机制发挥作用。模拟热量限制的药物包括 AMP 活化蛋白激酶激活剂(二甲双胍)和 mTOR 抑制剂(雷帕霉素),以及同时具有这两种效果的利美尼定。天然产品迷迭香酸具有抗糖化特性。与年龄有关的蛋白质交联被认为是老年疾病的致病因素。抗衰老医学是一个不断发展的领域,有多种药物和策略,需要根据临床经验和从延迟不良事件中获得的启示进行进一步的临床研究和长期跟踪。
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引用次数: 0
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Acta Dermatovenerologica Alpina Pannonica et Adriatica
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