Natural course

自然课程
  • 文章类型: Journal Article
    分化型外阴上皮内瘤变(dVIN)是人乳头瘤病毒(HPV)非依赖性外阴鳞状细胞癌(VSCC)的前体。鉴于dVIN的罕见发生率,关于确切癌症风险的信息有限。我们系统地回顾了dVIN患者的原发性和复发性VSCC风险,以及癌症发展的时间。根据PRISMA指南,系统搜索已进行到2021年7月。五名审稿人独立筛选标题文章,摘要和全文,然后使用预后研究质量(QUIPS)工具对选定的文章进行批判性评估。在455篇筛选的文章中,包括7个用于分析。dVIN中原发性VSCC的绝对风险在33%至86%之间变化,进展到VSCC的中位时间为9-23个月。dVIN相关VSCC发生VSCC复发的风险为32-94%,中位复发时间为13-32个月。总之,dVIN患者发生原发性和复发性VSCC的风险很高,且癌症进展时间短.提高认识,及时识别,因此,强烈建议对包括dVIN在内的HPV非依赖性外阴疾病进行积极治疗和密切随访.
    Differentiated vulvar intraepithelial neoplasia (dVIN) is the precursor of human papillomavirus (HPV)-independent vulvar squamous cell carcinoma (VSCC). Given the rare incidence of dVIN, limited information on the exact cancer risk is available. We systematically reviewed the primary and recurrent VSCC risk in patients with dVIN, as well as the time to cancer development. A systematic search was performed up to July 2021 according to the PRISMA guidelines. Five reviewers independently screened articles on title, abstract and full text, followed by critical appraisal of selected articles using the Quality in Prognostic Studies (QUIPS) tool. Of the 455 screened articles, 7 were included for analysis. The absolute risk for primary VSCC in dVIN varied between 33 and 86%, with a median time to progression to VSCC of 9-23 months. The risk of developing recurrent VSCC in dVIN associated VSCC was 32-94%, with a median time to recurrence of 13-32 months. In conclusion, patients with dVIN have a high risk of developing primary and recurrent VSCC with a short time to cancer progression. Increased awareness, timely recognition, aggressive treatment and close follow-up of HPV-independent vulvar conditions including dVIN is therefore strongly recommended.
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  • 文章类型: Journal Article
    抽搐的特点是突然,快速,经常性,无节奏的运动或发声,是儿童最常见的运动障碍。它们的发作通常在儿童时期,抽动通常会在一年内减少。然而,一些抽搐会持续存在并引起各种问题,例如社会尴尬,身体不适,或者情绪障碍,这可能会干扰日常活动和学校表现。此外,抽动障碍通常与共病神经精神症状有关,比抽动症状更有问题。不幸的是,对抽动障碍的误解和误解仍然存在于普通人群中。了解抽动障碍及其合并症对于为抽动患者提供适当的护理很重要。已经进行了一些研究来阐明临床过程,流行病学,和病理学,但是他们仍然没有得到很好的理解。本文旨在提供有关抽动和抽动障碍的概述,以及最近关于抽动障碍的发现,包括病史,定义,诊断,流行病学,病因学,诊断方法,合并症,治疗和管理,和鉴别诊断。
    Tics are characterized by sudden, rapid, recurrent, nonrhythmic movement or vocalization, and are the most common movement disorders in children. Their onset is usually in childhood and tics often will diminish within one year. However, some of the tics can persist and cause various problems such as social embarrassment, physical discomfort, or emotional impairments, which could interfere with daily activities and school performance. Furthermore, tic disorders are frequently associated with comorbid neuropsychiatric symptoms, which can become more problematic than tic symptoms. Unfortunately, misunderstanding and misconceptions of tic disorders still exist among the general population. Understanding tic disorders and their comorbidities is important to deliver appropriate care to patients with tics. Several studies have been conducted to elucidate the clinical course, epidemiology, and pathophysiology of tics, but they are still not well understood. This article aims to provide an overview about tics and tic disorders, and recent findings on tic disorders including history, definition, diagnosis, epidemiology, etiology, diagnostic approach, comorbidities, treatment and management, and differential diagnosis.
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  • 文章类型: Journal Article
    Taking the natural course of recurrent and fluctuating low back pain (LBP) seen in longitudinal studies of adults into consideration, the aetiology and development of LBP in children and adolescents also needs to be reflected in a long-term course. Therefore, a systematic critical literature review was undertaken to assess the natural course of LBP in the general population from childhood through adolescence to young adulthood.
    A systematic literature search was conducted in MEDLINE, EMBASE, CINAHL and PsycINFO with synonyms of search terms for 1) low back pain; 2) natural course; 3) cohort study and 4) children. Records in English, German, French, Danish, Swedish, and Norwegian were included. To assess the methodological quality of the studies, the NIH quality assessment checklist for cohort studies was adapted and risk of bias was assessed on a study level. Two authors independently reviewed selected studies, assessed quality, and extracted data. A synthesis of results in relation to the natural course of LBP was created.
    Totally, 3373 records were identified, eight articles were included for quality assessment, and finally, four studies of good to fair quality were included for synthesis of results. Indication of three common patterns of LBP were identified across studies and labelled as 1) ´children and adolescents with no LBP or low probability of LBP´ (49 to 53%), 2) ´children and adolescents with fluctuation of LBP´ (16 to 37%) and 3) ´children and adolescents with repeated reporting of LBP´ (< 1 to 10%).
    Although methodological heterogeneity, mainly due to different age ranges, an indication of a natural course of LBP was seen across studies. The majority of children and adolescents repeatedly reporting no or low probability of LBP. With recall periods between one week to three months and sampling rates ranging from one to four years, a very low rate repeatedly reported LBP, and approximately one-fifth to one-third of children and adolescents had fluctuating reports of LBP. A need of future research of LBP trajectories with short reporting period lengths and narrower sampling windows in a long-term perspective is emphasized in order to study childhood influences on the development of LBP throughout life.
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  • 文章类型: Case Reports
    带有“天际线”基底细胞层(PENS)的丘疹表皮痣是一种非常罕见的角质形成细胞痣,在大约50%的病例中与诸如神经系统症状等皮肤外发现有关。因此,它也被称为PENS综合征。临床上可见的过度角化丘疹和斑块在出生时或出生后不久就已经出现,而癫痫和智力低下等神经系统症状在儿童时期表现出来。遗传学表明性腺镶嵌是该疾病的可能原因。另一个假设是,基因突变可以发生在孟德尔性状中或通过副词遗传。
    Papular epidermal nevus with \"skyline\" basal cell layer (PENS) is a very rare type of keratinocytic nevus and is associated with extracutaneous findings such as neurological symptoms in about 50% of the cases. Therefore, it is also referred to as PENS syndrome. Clinically visible hyperkeratotic papules and plaques already appear at birth or shortly thereafter, while neurological symptoms such as epilepsy and mental retardation manifest themselves during childhood. Genetics suggests gonadal mosaicism as a possible cause for the disease. Another hypothesis is that genetic mutation can occur in a mendelian trait or through a paradominant inheritance.
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  • 文章类型: Journal Article
    BACKGROUND: The natural course of shoulder instability is still not entirely clear. We aimed in this review to analyse the current scientific evidence of the natural history of shoulder instability.
    METHODS: A systematic review of the English literature was performed using the PubMED database throughout January 2014. This review was guided, conducted and reported according to PRISMA criteria. The criteria for inclusion in the study were (1) the article was written in English, (2) the level of evidence was 1-4, (3) the article was available in full text, (4) the article investigated the natural history or course of shoulder instability, the outcome of non-operative management, or the regression of the shoulder symptoms to the mean. The methodological quality of each included study was individually assessed using a newly developed general assessment tool-Assessing the Methodological Quality of Published Papers (AMQPP).
    RESULTS: Eight articles related to shoulder instability met the inclusion criteria. Four papers were considered high-quality studies (evidence level 1 and 2). One paper assessed the natural history and the natural course of shoulder instability directly. The other studies indirectly assessed the natural history by studying non-operative and operative therapy trends. We found no articles which clearly referred to the role of \'regression to the mean\'.
    CONCLUSIONS: Following the natural history and the implementation of standardised non-operative treatment programmes are an effective therapy and superior to surgery in many cases. However, primary acute shoulder dislocation in young active individuals partaking in demanding physical activities could benefit from early surgical intervention. The AMQPP score works as a quick quality-checking tool which helps researchers to identify the key points in each paper and reach a decision regarding the eligibility of the paper more easily. The AMQPP scoring system is still open for further development and expansion. Level of evidence Level IV.
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  • 文章类型: Journal Article
    BACKGROUND: Patients with isolated mucosal cysts of the maxillary sinus (MMC) often undergo surgical treatment despite the absence of relevant symptoms. Some physicians believe that MMC might increase in size and cause complications in the future. The anticipated value of this study is to consolidate and improve the understanding of MMC based on published data and to contribute to avoiding unnecessary interventions.
    METHODS: We performed a comprehensive review of the literature regarding definition, etiology, epidemiology, natural course, and best treatment of MMC.
    RESULTS: Among the 988 papers found in the literature search, 33 studies were selected to be relevant. Among those studies, there are only a few prospective controlled studies. Their prevalence rates range broadly from 3.6% to 35.6% according to different diagnostic methods as well as different indications for imaging. Recent prospective studies showed no correlation of MMC with sinonasal complaints or Lund-Mackay computed tomography (CT) score. The natural course is characterized by a decrease in size of MMC in 30% of the cases, an unchanged status in 50% to 60%, and an increase in 8% to 20% of the cases.
    CONCLUSIONS: MMC are harmless, mostly asymptomatic lesions that usually do not need surgical treatment. If surgery is indicated, endonasal endoscopic techniques should be the gold-standard approach.
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