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弥漫性新生儿血管瘤病:文献中病例报告的循证综述。

Diffuse neonatal hemangiomatosis: an evidence-based review of case reports in the literature.

机构信息

University of Alabama at Birmingham, Department of Dermatology, Birmingham, Alabama 35294-0009, USA.

出版信息

J Am Acad Dermatol. 2012 Nov;67(5):898-903. doi: 10.1016/j.jaad.2012.01.018. Epub 2012 Feb 15.

Abstract

BACKGROUND

The term "diffuse neonatal hemangiomatosis" has been used historically to describe multifocal vascular lesions affecting the skin and viscera in infants.

OBJECTIVE

We hypothesized that many cases reported as diffuse neonatal hemangiomatosis did not have infantile hemangiomas (IH), but represented more recently described neonatal vascular diseases.

METHODS

A literature search was performed using PubMed database (1950-2009) with the terms "neonatal hemangiomatosis," "benign hemangiomatosis," and "diffuse hemangiomatosis." A total of 180 articles were identified. Exclusion criteria included disease onset later than 3 years of age and absence of multifocal skin involvement. In all, 73 cases were selected and categorized into 3 groups: IH/probable IH; multifocal lymphangioendotheliomatosis with thrombocytopenia (MLT)/probable MLT; and multifocal vascular lesions, not otherwise specified.

RESULTS

Of the 73 cases, 43 had IH/probable IH, 17 had MLT/probable MLT, and 13 had multifocal vascular lesions, not otherwise specified. The clinical outcomes of these groups differed in that two of 43 (5%) patients with IH died whereas 11 of 17 (65%) patients with MLT died (odds ratio 37.6, confidence interval 5.6-387.6, P value < .0001).

LIMITATIONS

This was a literature-based meta-analysis, which inherently has limitations of incomplete and inconsistently presented information.

CONCLUSIONS

Many cases reported in the literature as diffuse neonatal hemangiomatosis represent newly described multifocal vascular anomalies such as MLT, which has a strikingly higher mortality than IH. We propose the term "multifocal infantile hemangioma-with or without extracutaneous disease" instead of "diffuse neonatal hemangiomatosis" for multiple cutaneous IH. Accurate diagnosis of multifocal neonatal vascular lesions is imperative to facilitate appropriate evaluation, treatment, and prognosis.

摘要

背景

“弥漫性新生儿血管瘤病”这一术语历史上曾用于描述影响婴儿皮肤和内脏的多灶性血管病变。

目的

我们假设许多被报告为弥漫性新生儿血管瘤病的病例实际上并不属于婴儿血管瘤(IH),而是代表了最近描述的新生儿血管疾病。

方法

我们使用 PubMed 数据库(1950-2009 年)中的“新生儿血管瘤病”、“良性血管瘤病”和“弥漫性血管瘤病”等术语进行了文献检索。共确定了 180 篇文章。排除标准包括发病年龄晚于 3 岁以及缺乏多灶性皮肤受累。总共选择了 73 例病例,并将其分为 3 组:IH/可能的 IH;多灶性淋巴管内皮瘤伴血小板减少症(MLT)/可能的 MLT;和未特指的多灶性血管病变。

结果

在这 73 例病例中,有 43 例为 IH/可能的 IH,17 例为 MLT/可能的 MLT,13 例为未特指的多灶性血管病变。这些组的临床结局不同,43 例 IH/可能的 IH 中有 2 例(5%)死亡,而 17 例 MLT/可能的 MLT 中有 11 例(65%)死亡(比值比 37.6,置信区间 5.6-387.6,P 值<0.0001)。

局限性

这是一项基于文献的荟萃分析,固有地存在信息不完整和不一致的局限性。

结论

文献中报道的许多弥漫性新生儿血管瘤病病例实际上代表了新描述的多灶性血管异常,如 MLT,其死亡率明显高于 IH。我们建议用“多灶性婴儿血管瘤伴或不伴皮肤外疾病”来替代“弥漫性新生儿血管瘤病”,以描述多发性皮肤 IH。准确诊断多灶性新生儿血管病变对于促进适当的评估、治疗和预后至关重要。

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