生长受限或停止的婴儿血管瘤(IHMAG):临床和皮肤镜诊断线索的回顾性分析。

IF 2.5 4区 医学 Q2 DERMATOLOGY Dermatology practical & conceptual Pub Date : 2024-07-01 DOI:10.5826/dpc.1403a206
Iria Neri, Gionathan Orioni, Miriam Leuzzi, Elena Facchini, Elena Mengozzi, Marco Adriano Chessa
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引用次数: 0

摘要

导言:生长受限或停止的婴儿血管瘤(IHMAG)是婴儿血管瘤中的一个不寻常的亚群,由于常被误认为毛细血管畸形或其他实体而难以识别。迄今为止,仅有少量病例描述了 IHMAG 的皮肤镜特征:我们的研究旨在评估 79 例 IHMAG 的流行病学、临床和皮肤镜特征,重点关注患有节段性复杂 IHMAG 的新生儿和幼儿,并提供一个显著的皮肤镜诊断标准:本病例系列收集了2012年1月至2022年3月我院临床登记处记录的所有IHMAG病例:我们的研究共发现 79 例 IHMAG,其中 53 例(67.1%)为局部性,26 例(32.9%)为节段性。患者在随访期间出现了一些并发症,如溃疡和软组织异常。其中包括 1 例 PHACE 综合征和 2 例 LUMBAR 综合征。我们的研究强调了皮肤镜将新生儿IHMAG与婴幼儿血管瘤和毛细血管畸形区分开来的主要特征,并突出强调了毛细血管扩张不集中是显著的线索:这是文献中描述的关于这一罕见实体的大型病例系列。我们强调,节段性 IHMAG 可能与结构异常有关,尤其是在罕见的面部节段性定位中,可能会给诊断带来挑战。皮肤镜的使用让我们发现了IHMAG的典型体征,从而避免了使用侵入性方法,确保在新生儿节段性病例中及时怀疑综合征。
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Infantile Hemangioma with Minimal or Arrested Growth (IHMAG): A Retrospective Analysis of Clinical and Dermoscopic Diagnostic Clues.

Introduction: Infantile hemangioma with minimal or arrested growth (IHMAG) is an unusual subset of infantile hemangioma, difficult to recognize because they are often mistaken for capillary malformation or other entities. Dermoscopic features of IHMAG have been described only in small case series so far.

Objectives: The aim of our study was to evaluate epidemiological, clinical, and dermoscopic features in 79 cases of IHMAG with a specific focus on neonates and toddlers with segmental complicated IHMAG and to provide a remarkable dermoscopic criterion to achieve diagnosis.

Methods: This case series collected all the cases of IHMAG recorded in our Clinical Registry from January 2012 to March 2022.

Results: A total of 79 cases of IHMAG were identified in our study; 53 (67.1%) were localized and 26 (32.9 %) were segmental. Patients showed some complications during follow-up such as ulceration and soft tissue anomalies. One PHACE syndrome and two LUMBAR syndromes were included. Our study highlights the main dermoscopic features differentiating IHMAG from infantile hemangiomas and capillary malformations in neonatal patients, highlighting the presence of enlarged unfocused telangiectatic vessels as remarkable clues.

Conclusions: This is a large case series described in the literature about this rare entity. We emphasize that segmental IHMAG may be associated with structural abnormalities and may pose a diagnostic challenge especially in its rare facial segmental localization. The use of dermoscopy allowed us to find typical signs for IHMAG, thus avoiding the execution of invasive methods and ensuring the prompt suspicion of a syndrome in segmental neonatal cases.

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