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多灶性婴儿血管瘤的病变形态学

Lesion Morphology in Multifocal Infantile Hemangiomas.

作者信息

Reimer Antonia, Hoeger Peter H

机构信息

Department of Pediatric Dermatology, Catholic Children's Hospital Wilhelmstift, Hamburg, Germany.

出版信息

Pediatr Dermatol. 2016 Nov;33(6):621-626. doi: 10.1111/pde.12956. Epub 2016 Sep 7.

Abstract

BACKGROUND/OBJECTIVES: Multifocal infantile hemangiomas (MIHs; previously called neonatal hemangiomatosis) can be associated with extracutaneous hemangiomas. We observed different morphologic types of hemangiomas in children with MIHs and sought to find out whether they are related to the clinical course.

METHODS

This was a retrospective study of 103 infants with MIHs and a control group of 261 age-matched patients with solitary focal infantile hemangiomas (IHs) seen at an academic pediatric dermatology department between 2004 and 2014.

RESULTS

Two morphologic subtypes of hemangiomas were identified: miliary focal hemangiomas (MFHs; small, lens shaped) in 58 of 103 MIH patients (56.3%), and classical nonmiliary focal IHs (NMIHs; larger, irregularly shaped) in 17 of 103 patients (16.5%). MIHs featuring both types (mixed type) were observed in 28 of 103 patients (27.2%). MFH lesions were significantly smaller (mean 5.3 mm [range 1-20 mm] vs 22.0 mm [range 2-100 mm]), more numerous (23.4 ± 27.3 [range 5-175] vs 7.4 ± 2.8 [range 5-15] p < 0.001), and occurred up to an older age (6.0 ± 5.8 months [range 0-27 months] vs 3.8 ± 2.6 months [range 0-9 months]) than NMIHs. There was a weakly positive correlation between the number and presence of extracutaneous IHs in children with MFHs. Significantly more children with MIHs were delivered preterm than those with solitary IHs.

CONCLUSIONS

The number of IHs correlates inversely with their size. MFHs follow a clinical course different from that of classical IHs, are associated with prematurity, and may confer greater risk of extracutaneous hemangiomas. Miliary hemangiomas thus appear to present a separate IH subset requiring special attention.

摘要

背景/目的:多灶性婴儿血管瘤(MIHs;以前称为新生儿血管瘤病)可能与皮肤外血管瘤有关。我们观察了患有MIHs的儿童中不同形态类型的血管瘤,并试图找出它们是否与临床病程相关。

方法

这是一项对103例患有MIHs的婴儿以及261例年龄匹配的孤立性局灶性婴儿血管瘤(IHs)患者的回顾性研究,这些患者于2004年至2014年在一家学术性儿科皮肤科就诊。

结果

确定了两种血管瘤形态学亚型:103例MIH患者中有58例(56.3%)为粟粒状局灶性血管瘤(MFHs;小,透镜状),103例患者中有17例(16.5%)为经典非粟粒状局灶性IHs(NMIHs;较大,不规则形状)。103例患者中有28例(27.2%)观察到两种类型均有的MIHs(混合型)。MFH病变明显更小(平均5.3毫米[范围1 - 20毫米]对22.0毫米[范围2 - 100毫米]),数量更多(23.4 ± 27.3[范围5 - 175]对7.4 ± 2.8[范围5 - 15],p < 0.001),并且出现的年龄比NMIHs更大(6.0 ± 5.8个月[范围0 - 27个月]对3.8 ± 2.6个月[范围0 - 9个月])。患有MFHs的儿童中皮肤外IHs的数量与存在情况之间存在弱正相关。患有MIHs的儿童早产的比例明显高于患有孤立性IHs的儿童。

结论

IHs的数量与其大小呈负相关。MFHs的临床病程与经典IHs不同,与早产有关,并且可能带来更大的皮肤外血管瘤风险。因此,粟粒状血管瘤似乎呈现出一个需要特别关注的单独的IH子集。

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