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本文引用的文献

1
Historical and contemporary management of infantile hemangiomas: a single-center experience.婴儿血管瘤的历史与现代治疗:单中心经验
Front Pharmacol. 2024 Feb 2;15:1280948. doi: 10.3389/fphar.2024.1280948. eCollection 2024.
2
Analysis of cytokine profiles in sera of single and multiple infantile hemangioma.分析单发和多发婴幼儿血管瘤患儿血清细胞因子谱。
J Dermatol. 2023 Jul;50(7):906-911. doi: 10.1111/1346-8138.16781. Epub 2023 Mar 27.
3
ISSVA Classification of Vascular Anomalies and Molecular Biology.ISSVA 血管异常分类与分子生物学。
Int J Mol Sci. 2022 Feb 21;23(4):2358. doi: 10.3390/ijms23042358.
4
Analysis of onset and clinical characteristics in Japanese patients with infantile hemangioma.分析日本婴儿血管瘤患者的发病和临床特征。
Drug Discov Ther. 2021 Sep 22;15(4):210-213. doi: 10.5582/ddt.2021.01066. Epub 2021 Aug 26.
5
Japanese Clinical Practice Guidelines for Vascular Anomalies 2017.日本 2017 年血管异常临床实践指南
J Dermatol. 2020 May;47(5):e138-e183. doi: 10.1111/1346-8138.15189. Epub 2020 Mar 22.
6
Risk factors for infantile hemangioma: a meta-analysis.婴儿血管瘤的危险因素:荟萃分析。
World J Pediatr. 2020 Aug;16(4):377-384. doi: 10.1007/s12519-019-00327-2. Epub 2019 Dec 18.
7
Distribution analysis of infantile hemangioma or capillary malformation on the head and face in Japanese patients.日本患者头面部婴幼儿血管瘤或毛细血管畸形的分布分析。
J Dermatol. 2019 Oct;46(10):849-852. doi: 10.1111/1346-8138.15051. Epub 2019 Aug 16.
8
Late ulceration of residual abortive infantile haemangioma: a rare complication.残留性消退期婴儿血管瘤的晚期溃疡形成:一种罕见的并发症。
Br J Dermatol. 2019 Aug;181(2):395-396. doi: 10.1111/bjd.17717. Epub 2019 Apr 22.
9
Recent progress in studies of infantile hemangioma.婴幼儿血管瘤研究的最新进展。
J Dermatol. 2010 Apr;37(4):283-98. doi: 10.1111/j.1346-8138.2010.00813.x.
10
Abortive hemangiomas. Description of clinical and pathological findings with special emphasis on dermoscopy.夭折性血管瘤。临床和病理表现描述,特别强调皮肤镜检查。
Eur J Dermatol. 2010 Jul-Aug;20(4):497-500. doi: 10.1684/ejd.2010.0959. Epub 2010 Apr 19.

出生后无增殖的婴儿血管瘤分析。

Analysis of infantile hemangioma without proliferation after birth.

作者信息

Inada Yusuke, Kawaguchi Ami, Kunimoto Kayo, Hara Tomoyuki, Inaba Yutaka, Yamamoto Yuki, Kakimoto Nobuyuki, Suenaga Tomohiro, Tokuhara Daisuke, Jinnin Masatoshi

机构信息

Department of Dermatology, Wakayama Medical University, 811-1 Kimiidera, Wakayama, Wakayama, Japan.

Department of Pediatrics, Wakayama Medical University, 811-1 Kimiidera, Wakayama, Wakayama, Japan.

出版信息

GHM Open. 2024 Nov 30;4(2):80-83. doi: 10.35772/ghmo.2023.01022.

DOI:10.35772/ghmo.2023.01022
PMID:40144968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11933936/
Abstract

Infantile hemangiomas (IHs) are the most common benign tumors of infancy, occurring in approximately 5-10% of the population. Among what appear to be typical IHs with proliferative and involuting phases, we noticed that there are also IHs that are already present at birth and regress without proliferating. We therefore aimed to determine the frequency and clinical characteristics of this type of IH. A retrospective study was conducted on 176 lesions of 137 Japanese patients with IH. As a result, six lesions (3.4%) in three patients with IH (2.1%) were already present at birth and lacked subsequent proliferation. Analysis of the clinical characteristics of IHs without proliferation revealed that they are significantly less common in the head and neck region, which is the preferred site of the tumor, than typical IHs with proliferation (0% 42.9%, < 0.05 by Fisher's exact test). This suggests that when the clinical course of IH is uncommon, their distribution can also be atypical. Furthermore, all of the IHs without proliferation were superficial types, and there were no deep types in this cohort. This study demonstrates that the clinical course of IH can be diverse, and that very rarely there can be a type of IH that does not grow after birth. It may be necessary to consider conducting a detailed interview for the growth history at the first visit for the possibility of such a type of IH without proliferation, as it is likely that they can be followed up without the need for treatment.

摘要

婴儿血管瘤(IHs)是婴儿期最常见的良性肿瘤,发病率约为5%-10%。在看似具有增殖期和消退期的典型IHs中,我们注意到也有一些IHs在出生时就已存在,且不经过增殖就消退。因此,我们旨在确定这类IH的发生率及临床特征。对137例日本IH患者的176处病损进行了一项回顾性研究。结果,3例(2.1%)IH患者的6处病损(3.4%)在出生时就已存在,且随后未出现增殖。对无增殖的IHs临床特征分析显示,与有增殖的典型IHs相比,其在肿瘤好发部位头颈部明显少见(0%对42.9%,Fisher精确检验P<0.05)。这表明,当IH的临床病程不常见时,其分布也可能不典型。此外,所有无增殖的IHs均为浅表型,该队列中无深部型。本研究表明,IH的临床病程可能多种多样,且极少数情况下可能存在出生后不生长的IH类型。对于这种无增殖的IH类型,初诊时可能有必要详细询问生长史,因为这类患者可能无需治疗即可随访观察。