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小儿耳血管肉瘤:一例罕见病例报告及文献综述

Pediatric Auricular Angiosarcoma: A Rare Case Report and Review of the Literature.

作者信息

Mayangsari Ika Dewi, Sriyana Ayu Astria, Adham Marlinda, Priyono Harim, Rahmanda Aris, Chozie Novie Amelia, Saraswati Meilania, Suroyo Indrati

机构信息

Department of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine University of Indonesia - Cipto Mangunkusumo Hospital, Jakarta, Indonesia.

Department of Pediatrics, Faculty of Medicine University of Indonesia - Cipto Mangunkusumo Hospital, Jakarta, Indonesia.

出版信息

Case Rep Oncol. 2025 Mar 3;18(1):429-435. doi: 10.1159/000543993. eCollection 2025 Jan-Dec.

DOI:10.1159/000543993
PMID:40160701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11952820/
Abstract

INTRODUCTION

Limited evidence exists regarding the clinical characteristics of auricular angiosarcoma in the pediatric population. To our knowledge, this represents the inaugural case report of auricular angiosarcoma in early childhood. This report aims to delineate the unique clinical features and findings associated with pediatric auricular angiosarcoma.

CASE PRESENTATION

We report a 7-year-old girl presented with a 2-year history of an enlarging, intermittently painful purplish-red mass in the left ear canal and undergo surgery with adjuvant chemotherapy.

CONCLUSION

Although a rarity, auricular angiosarcoma can manifest in pediatric patients, necessitating vigilant consideration for diagnosis in this population. The evaluation and management of auricular angiosarcoma in pediatric cases demands heightened caution due to the patients' young age and the high risk of recurrence and metastases following primary treatments.

摘要

引言

关于儿童耳廓血管肉瘤的临床特征,现有证据有限。据我们所知,这是首例关于幼儿耳廓血管肉瘤的病例报告。本报告旨在阐述与儿童耳廓血管肉瘤相关的独特临床特征和发现。

病例介绍

我们报告一名7岁女孩,左耳耳道有一个逐渐增大、间歇性疼痛的紫红色肿块,病史2年,并接受了手术及辅助化疗。

结论

尽管罕见,但耳廓血管肉瘤可在儿科患者中出现,因此需要对此人群进行警惕性诊断。由于患儿年龄小且初次治疗后复发和转移风险高,儿科病例中耳廓血管肉瘤的评估和管理需要格外谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a8/11952820/ceb1db8faa08/cro-2025-0018-0001-543993_F03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a8/11952820/19a91fe4547f/cro-2025-0018-0001-543993_F01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a8/11952820/ee5b0b906def/cro-2025-0018-0001-543993_F02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a8/11952820/ceb1db8faa08/cro-2025-0018-0001-543993_F03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a8/11952820/19a91fe4547f/cro-2025-0018-0001-543993_F01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a8/11952820/ee5b0b906def/cro-2025-0018-0001-543993_F02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a8/11952820/ceb1db8faa08/cro-2025-0018-0001-543993_F03.jpg

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本文引用的文献

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Current Management of Angiosarcoma: Recent Advances and Lessons From the Past.血管肉瘤的当前管理:最新进展与历史教训
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Angiosarcoma of the Auricle in a Patient with Xeroderma Pigmentosum Variant.着色性干皮病变异型患者的耳廓血管肉瘤
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Recurrent cutaneous angiosarcoma of the ear masquerading as atypical fibroxanthoma.耳部复发性皮肤血管肉瘤伪装成非典型纤维黄色瘤。
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Angiosarcoma of the auricle.耳廓血管肉瘤
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Dermoscopic pattern of radiation-induced angiosarcoma (RIA).放射性诱导血管肉瘤(RIA)的皮肤镜表现。
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