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[伴有先天性小耳畸形和外耳道闭锁的耳后畸胎瘤:一例报告]

[Retroauricular teratoma with congenital microtia and ankylotia: a case report].

作者信息

Shi Shujing, Liang Hua, Xu Li, Zhang Yaqing, Fan Zhitao, Tian Yongtao, Wang Chunhua

出版信息

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2020 Apr;34(4):372-373. doi: 10.13201/j.issn.2096-7993.2020.04.021.

DOI:10.13201/j.issn.2096-7993.2020.04.021
PMID:32842237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10127768/
Abstract

Teratoma is a germ cell tumor, which is rare behind the ear. We described a rare case of retroauricular teratoma accompanied with congenital malformation of external and middle ear and cholesteatoma of middle ear in a 13-years-old girl. Congenital microtia and ankylotia of right ear was found since childhood, suppuration occurred repeatedly behind the right ear 1 year ago. Temporal bone CT and MRI scan revealed congenital malformation of middle ear and cholesteatoma of middle ear. Cystic mass containing a tooth was found intraoperatively. The pathological results showed that it was benign cystic teratoma. It showed no evidence of recurrence on the patient during 3 months follow-up.

摘要

畸胎瘤是一种生殖细胞肿瘤,耳后较为罕见。我们描述了一例罕见的耳后畸胎瘤病例,该病例发生在一名13岁女孩身上,同时伴有外耳和中耳先天性畸形以及中耳胆脂瘤。该女孩自幼即被发现右耳先天性小耳畸形及外耳道闭锁,1年前右耳后反复出现化脓。颞骨CT和MRI扫描显示中耳先天性畸形及中耳胆脂瘤。术中发现一个含有牙齿的囊性肿块。病理结果显示为良性囊性畸胎瘤。在3个月的随访中,患者未出现复发迹象。

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引用本文的文献

1
[Mature teratoma of the auricle in children: a case report].[儿童耳廓成熟性畸胎瘤:一例报告]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2020 Oct;34(10):950-951. doi: 10.13201/j.issn.2096-7993.2020.10.020.

本文引用的文献

1
Microtia in a Chinese Specialty Clinic Population: Clinical Heterogeneity and Associated Congenital Anomalies.中国特色临床诊所中小耳畸形患者:临床异质性及相关先天性畸形。
Plast Reconstr Surg. 2018 Dec;142(6):892e-903e. doi: 10.1097/PRS.0000000000005066.
2
The genetics of auricular development and malformation: new findings in model systems driving future directions for microtia research.耳廓发育与畸形的遗传学:模型系统中的新发现引领小耳畸形研究的未来方向
Eur J Med Genet. 2014 Aug;57(8):394-401. doi: 10.1016/j.ejmg.2014.05.003. Epub 2014 May 29.