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伴有颅内扩展的口腔畸胎瘤(上颌寄生胎):两例报告

Oral teratoma (epignathus) with intracranial extension: a report of two cases.

作者信息

Smith N M, Chambers S E, Billson V R, Laing I, West C P, Bell J E

机构信息

Department of Paediatric, Pathology and Cytogenetics, Royal Hospital for Sick Children, Edinburgh, U.K.

出版信息

Prenat Diagn. 1993 Oct;13(10):945-52. doi: 10.1002/pd.1970131008.

DOI:10.1002/pd.1970131008
PMID:8309901
Abstract

Epignathi are unusual congenital tumours presenting as oropharyngeal masses, often resulting in rapid asphyxia following birth. Occasionally, intracranial extension of the tumour is present, and two such cases are described. The presence of this complication, diagnosable by ultrasound examination, indicates that aggressive surgical treatment is inappropriate.

摘要

口鼻寄生胎是一种罕见的先天性肿瘤,表现为口咽肿块,常导致出生后迅速窒息。偶尔,肿瘤会向颅内扩展,本文描述了两例这样的病例。这种并发症可通过超声检查诊断,其存在表明积极的手术治疗是不合适的。

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Oral teratoma (epignathus) with intracranial extension: a report of two cases.伴有颅内扩展的口腔畸胎瘤(上颌寄生胎):两例报告
Prenat Diagn. 1993 Oct;13(10):945-52. doi: 10.1002/pd.1970131008.
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Antenatal sonographic diagnosis of epignathus at 15 weeks of pregnancy.孕15周时产前超声诊断出胎儿颈部寄生胎。
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Early second-trimester diagnosis of intracranial teratoma.孕中期早期颅内畸胎瘤的诊断
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Epignathus with oropharynx destruction.伴有口咽破坏的上颌寄生胎。
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An autopsy case of epignathus (immature teratoma of the soft palate) with intracranial extension but without brain invasion: case report and literature review.1例伴有颅内扩展但无脑侵犯的上颌咽囊肿(软腭未成熟畸胎瘤)尸检病例:病例报告及文献复习
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A rare case of oropharyngeal teratoma diagnosed antenatally with MRI.1例产前经磁共振成像诊断的口咽畸胎瘤罕见病例。
J Clin Imaging Sci. 2014 Mar 21;4:15. doi: 10.4103/2156-7514.129261. eCollection 2014.
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Intraoral teratoma in a newborn presenting as severe respiratory distress.一名表现为严重呼吸窘迫的新生儿口腔内畸胎瘤。
BMJ Case Rep. 2013 Mar 25;2013:bcr2013008735. doi: 10.1136/bcr-2013-008735.
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J Maxillofac Oral Surg. 2009 Mar;8(1):60-3. doi: 10.1007/s12663-009-0015-x. Epub 2009 Jun 10.
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Obstet Gynecol Int. 2009;2009:180643. doi: 10.1155/2009/180643. Epub 2009 Apr 2.
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Hamartomas, teratomas and teratocarcinosarcomas of the head and neck: Report of 3 new cases with clinico-pathologic correlation, cytogenetic analysis, and review of the literature.头颈部错构瘤、畸胎瘤及畸胎癌肉瘤:3例新病例报告并结合临床病理、细胞遗传学分析及文献复习
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