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葡萄酒色斑的无创性诊断技术。

Noninvasive diagnostic techniques of port wine stain.

机构信息

Private Practitioner, Ahmedabad, India.

Department of Dermatology, Bangalore Medical College and Research Institute, Bangalore, India.

出版信息

J Cosmet Dermatol. 2021 Jul;20(7):2006-2014. doi: 10.1111/jocd.14087. Epub 2021 Mar 31.

Abstract

Port-wine stain (PWS) is a benign capillary malformation that most commonly occurs in the head and neck. It is present at birth and progresses over time. It is formed by progressive dilatation of post-capillary venules and is associated with hypertrophy and nodularity with increasing age, leading to cosmetic disfigurement and psychological aggravation. It is caused by genetic mosaicism in GNAQ and GNA11 genes. Histopathology is the gold standard for assessment of PWS but it is invasive and may cause scarring. Inadequate characterization of the lesions may predispose to inadequate treatment protocols as well as higher treatment dosages. Clinical evaluation of treatment efficacy is subjective and may not be a representative of actual results. Therefore, an objective visualization modality is required. With evolving technology, numerous optical instruments have been developed for objective evaluation and visualization of subsurface structures. These include VISIA-CR™ system, videodermoscopy, high-frequency ultrasound (HFUS), laser speckle contrast imaging (LSCI), reflectance spectrophotometers and tristimulus colorimeter, laser Doppler flowmetry (LDF), cross-polarized diffuse reflectance imaging system (CDR), reflectance confocal microscopy (RCM), optical coherence tomography (OCT), and spatial frequency domain imaging (SFDI). These semi-quantitative modes of diagnosis are complementary to each other. Some can be used in the clinical setting while others, due to high instrument cost, are limited to the research settings. In this review, we bring to you a brief overview of noninvasive diagnostic modalities in PWS.

摘要

葡萄酒色斑(PWS)是一种常见于头颈部的良性毛细血管畸形。它在出生时就存在,并随着时间的推移而进展。它是由毛细血管后微静脉的渐进性扩张形成的,并且随着年龄的增长与肥大和结节形成有关,导致美容缺陷和心理恶化。它是由 GNAQ 和 GNA11 基因的遗传嵌合体引起的。组织病理学是评估 PWS 的金标准,但它具有侵袭性,可能导致疤痕。对病变的特征描述不足可能导致治疗方案不足以及治疗剂量增加。治疗效果的临床评估是主观的,可能无法代表实际结果。因此,需要一种客观的可视化方式。随着技术的不断发展,已经开发出许多光学仪器用于客观评估和可视化皮下结构。这些包括 VISIA-CR™系统、视频皮肤镜、高频超声(HFUS)、激光散斑对比成像(LSCI)、反射分光光度计和三刺激比色计、激光多普勒血流仪(LDF)、交叉偏振漫反射成像系统(CDR)、反射共聚焦显微镜(RCM)、光学相干断层扫描(OCT)和空间频率域成像(SFDI)。这些半定量诊断模式相互补充。有些可以在临床环境中使用,而有些由于仪器成本高,仅限于研究环境。在这篇综述中,我们为您简要介绍了 PWS 的非侵入性诊断模式。

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