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神经皮肤疾病多学科门诊:葡萄牙一家儿科三级医院的五年经验。

Multidisciplinary Outpatient Clinic of Neurocutaneous Diseases: Five-year Experience of a Pediatric Tertiary Hospital in Portugal.

机构信息

Pediatrics Department. Hospital Dona Estefânia. Centro Hospitalar Universitário de Lisboa Central. Lisbon. Portugal.

Multidisciplinary Outpatient Clinic of Neurocutaneous Diseases. Hospital Dona Estefânia. Centro Hospitalar Universitário de Lisboa Central. Lisbon; Nephrology Department. Hospital Dona Estefânia. Centro Hospitalar Universitário de Lisboa Central. Lisbon. Portugal.

出版信息

Acta Med Port. 2024 Mar 1;37(3):187-197. doi: 10.20344/amp.19063. Epub 2023 Jun 9.

Abstract

INTRODUCTION

Neurocutaneous syndromes (NCS) are a heterogeneous group of conditions with multiorgan involvement and diverse manifestations, evolving throughout life with significant morbidity. A multidisciplinary approach to NCS patients has been advocated, although a specific model is not yet established. The aim of this study was 1) to describe the organization of the recently created Multidisciplinary Outpatient Clinic of Neurocutaneous Diseases (MOCND) at a Portuguese pediatric tertiary hospital; 2) to share our institutional experience focusing on the most common conditions, neurofibromatosis type 1 (NF1) and tuberous sclerosis complex (TSC); 3) to analyze the advantages of a multidisciplinary center and approach in NCS.

METHODS

Retrospective analysis of 281 patients enrolled in the MOCND over the first five years of activity (October 2016 to December 2021), reviewing genetics, family history, clinical features, complications, and therapeutic strategies for NF1 and TSC.

RESULTS

The clinic works weekly with a core team of pediatricians and pediatric neurologists supported by other specialties as needed. Of the 281 patients enrolled, 224 (79.7%) had identifiable syndromes such as NF1 (n = 105), TSC (n = 35), hypomelanosis of Ito (n = 11), Sturge-Weber syndrome (n = 5), and others. In NF1 patients, 41.0% had a positive family history, all manifested café-au-lait macules, 38.1% neurofibromas with 45.0% being large plexiform neurofibromas. Sixteen were under treatment with selumetinib. Genetic testing was performed in 82.9% of TSC patients with pathogenic variants found in TSC2 gene in 72.4% patients (82.7% if considered contiguous gene syndrome). Family history was positive in 31.4%. All TSC patients presented hypomelanotic macules and fulfilled diagnostic criteria. Fourteen patients were being treated with mTOR inhibitors.

CONCLUSION

Offering a systematic and multidisciplinary approach to NCS patients enables timely diagnosis, promotes a structured follow-up, and encourages discussion to outline management plans for optimal care to every patient, with significant impact on the quality of life of patients and families.

摘要

简介

神经皮肤综合征(NCS)是一组具有多种器官受累和多种表现的异质性疾病,其在整个生命过程中都在发展,并伴有严重的发病率。尽管尚未建立特定的模型,但提倡对 NCS 患者进行多学科治疗。本研究的目的是:1)描述葡萄牙儿科三级医院新成立的神经皮肤疾病多学科门诊(MOCND)的组织情况;2)分享我们机构在最常见疾病(神经纤维瘤病 1 型(NF1)和结节性硬化症复合征(TSC))方面的经验;3)分析多学科中心和方法在 NCS 中的优势。

方法

回顾性分析 2016 年 10 月至 2021 年 12 月 MOCND 成立后五年内的 281 名患者,对 NF1 和 TSC 的遗传学、家族史、临床特征、并发症和治疗策略进行分析。

结果

该诊所每周工作一次,核心团队由儿科医生和儿科神经科医生组成,根据需要由其他专业人员提供支持。在 281 名入组患者中,224 名(79.7%)患有可识别的综合征,如 NF1(n=105)、TSC(n=35)、伊藤色素减退症(n=11)、Sturge-Weber 综合征(n=5)和其他疾病。在 NF1 患者中,41.0%有阳性家族史,所有患者均有咖啡牛奶斑,38.1%有神经纤维瘤,其中 45.0%为大丛状神经纤维瘤。16 名患者正在接受 selumetinib 治疗。82.9%的 TSC 患者进行了基因检测,发现 TSC2 基因的致病性变异,72.4%的患者(如果考虑连续基因综合征,则为 82.7%)存在阳性家族史。所有 TSC 患者均有色素减退斑,符合诊断标准。14 名患者正在接受 mTOR 抑制剂治疗。

结论

为 NCS 患者提供系统的多学科治疗方法,可以实现及时诊断,促进结构化随访,并鼓励讨论制定最佳治疗计划,为每位患者提供最佳护理,从而显著提高患者和家庭的生活质量。

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