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成人蓝色橡皮疱痣综合征的临床特征:系统综述

Clinical characteristics of blue rubber bleb nevus syndrome in adults: systematic scoping review.

作者信息

Kozai Landon, Nishimura Yoshito

机构信息

Department of Medicine, John A. Burns School of Medicine, University of Hawai'i, Honolulu, HI, USA.

出版信息

Scand J Gastroenterol. 2023 Jul-Dec;58(10):1108-1114. doi: 10.1080/00365521.2023.2214263. Epub 2023 May 21.

Abstract

BACKGROUND

Blue rubber bleb nevus syndrome (BRBNS) is a rare systemic vascular anomaly mainly affecting the skin, central nervous system and gastrointestinal tracts. Its clinical presentation and characteristics in adult patients are unclear.

AIM

To clarify the characteristics of BRBNS in adult patients with a focus on gastrointestinal symptoms.

METHODS

Following the PRISMA Extension for Scoping Reviews, we searched MEDLINE and EMBASE for all peer-reviewed articles using keywords including 'Blue rubber bleb nevus syndrome' from their inception to 28 December 2021.

RESULTS

Ninety-nine articles, including 3 observational studies and 101 cases from case reports and series, were included. Observational studies were consistently with small sample sizes, and there was only one prospective study to show the effectiveness of sirolimus in BRBNS. Common clinical presentations included anemia (50.5%) and melena (26.5%). While skin findings were known to be representative of BRBNS, only 57.4% had known vascular malformation. The diagnosis was primarily made clinically, with only 1% being diagnosed with BRBNS through genetic sequencing. Distribution of BRBNS-related lesions were variable, but predominantly oral (55.9%), followed by small bowel (49.5%), colorectal (35.6%) and stomach (26.7%) vascular malformations.

CONCLUSION

While it has been underrecognized, adult BRBNS could be a culprit for refractory microcytic anemia or occult gastrointestinal bleeding. Further studies are critical to establish a uniform understanding of diagnosis and treatment for those with adult BRBNS. The utility of genetic testing in adult BRBNS diagnosis and the patient characteristics that may benefit from sirolimus, a potentially curative agent, remain to be clarified.

摘要

背景

蓝橡皮疱痣综合征(BRBNS)是一种罕见的系统性血管异常疾病,主要累及皮肤、中枢神经系统和胃肠道。其在成年患者中的临床表现和特征尚不清楚。

目的

以胃肠道症状为重点,阐明成年BRBNS患者的特征。

方法

按照系统综述扩展版的PRISMA指南,我们检索了MEDLINE和EMBASE数据库,以查找从建库至2021年12月28日期间所有使用包括“蓝橡皮疱痣综合征”在内的关键词的同行评审文章。

结果

共纳入99篇文章,包括3项观察性研究以及来自病例报告和系列研究的101例病例。观察性研究样本量均较小,仅有一项前瞻性研究显示西罗莫司对BRBNS有效。常见临床表现包括贫血(50.5%)和黑便(26.5%)。虽然皮肤表现是BRBNS的典型特征,但只有57.4%的患者已知存在血管畸形。诊断主要基于临床,仅1%的患者通过基因测序确诊为BRBNS。BRBNS相关病变的分布各异,但主要集中在口腔(55.9%),其次是小肠(49.5%)、结肠直肠(35.6%)和胃(26.7%)的血管畸形。

结论

尽管BRBNS一直未得到充分认识,但成年BRBNS可能是难治性小细胞贫血或隐匿性胃肠道出血的病因。进一步的研究对于统一认识成年BRBNS患者的诊断和治疗至关重要。基因检测在成年BRBNS诊断中的作用以及可能从潜在治愈药物西罗莫司中获益的患者特征仍有待阐明。

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