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婴儿牙源性黏液瘤:一种特殊的实体。

Infant Odontogenic Myxoma: a specific entity.

作者信息

Kadlub Natacha, Mbou Valere Belle, Leboulanger Nicolas, Lepointe Hubert Ducou, Ansari Edward, L'hermine Aurore Coulomb, Davrou Julien, Vazquez Marie-Paule, Picard Arnaud

机构信息

APHP (Head: Prof. Vazquez), Hôpital Necker Enfants Malades, Service de chirurgie Maxillofaciale, Paris 75015, France; Université Paris V, UFR de Médecine Paris Descartes, Paris 75006, France; Centre de références des malformations de la face et de la cavité buccale (Head: Prof. Vazquez), Paris 75015, France; Laboratoire de Physiopathologie orale et Moléculaire (Head: Prof. Berdal), INSERM, UMRS 872, Equipe 5, Centre de recherche des Cordeliers, Paris 75006, France.

APHP (Head: Prof. Coulomb L'Herminé), Hôpital Armand Trousseau, Service de cytologie et anatomopathologie, Paris 75012, France.

出版信息

J Craniomaxillofac Surg. 2014 Dec;42(8):2082-6. doi: 10.1016/j.jcms.2013.07.019. Epub 2014 Jan 12.

DOI:10.1016/j.jcms.2013.07.019
PMID:24429059
Abstract

INTRODUCTION

In children, and specifically in infants, odontogenic myxomas are extremely rare. In infants, myxoma seems to display mostly the same clinical, radiological and pathological characteristics. This paper presents a series of odontogenic myxomas in infant patients.

MATERIALS AND METHODS

Four infant patients were included in this retrospective study. The clinical, radiological and pathological presentation was characterized and the treatment analysed.

RESULTS

All patients presented with a rapidly evolving paranasal swelling. CT-scan showed a maxillary homogeneous unilocular and intraosseous tumour. In all cases, pathological examination revealed a loose myxoid stroma within stellate and spindle shaped cells. All patients underwent conservative surgery through a vestibular approach.

CONCLUSION

This patient series and a review of the literature demonstrates that odontogenic myxoma is specific in infant. We propose the name of Infant Odontogenic Myxoma for this entity.

摘要

引言

在儿童中,尤其是婴儿,牙源性黏液瘤极为罕见。在婴儿中,黏液瘤似乎大多表现出相同的临床、放射学和病理学特征。本文介绍了一系列婴儿患者的牙源性黏液瘤。

材料与方法

本回顾性研究纳入了4例婴儿患者。对其临床、放射学和病理学表现进行了特征描述,并对治疗方法进行了分析。

结果

所有患者均表现为迅速发展的鼻旁肿胀。CT扫描显示上颌骨内有一个均匀的单房性骨内肿瘤。在所有病例中,病理检查均显示星状和梭形细胞内有疏松的黏液样基质。所有患者均通过前庭入路接受了保守手术。

结论

该患者系列及文献回顾表明,牙源性黏液瘤在婴儿中具有特异性。我们建议将该实体命名为婴儿牙源性黏液瘤。

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Infant Odontogenic Myxoma: a specific entity.婴儿牙源性黏液瘤:一种特殊的实体。
J Craniomaxillofac Surg. 2014 Dec;42(8):2082-6. doi: 10.1016/j.jcms.2013.07.019. Epub 2014 Jan 12.
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Conservative treatment of odontogenic myxoma.牙源性黏液瘤的保守治疗
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Odontogenic myxoma: diagnostic and therapeutic challenges in paediatric and adult patients--a case series and review of the literature.牙源性黏液瘤:儿童和成人患者的诊断和治疗挑战——病例系列和文献复习。
J Craniomaxillofac Surg. 2012 Apr;40(3):271-6. doi: 10.1016/j.jcms.2011.04.009. Epub 2011 May 31.
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An expanded odontogenic myxoma in maxilla.上颌骨的膨胀性牙源性黏液瘤。
Stomatologija. 2010;12(4):122-8.
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Peripheral odontogenic myxoma.外周性牙源性黏液瘤
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[Odontogenic myxoma of the maxilla: report of a case].[上颌骨牙源性黏液瘤:1例报告]
Odontostomatol Trop. 2017 Mar;40(157):34-8.
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Kulak Burun Bogaz Ihtis Derg. 2007;17(5):294-7.
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J Oral Pathol Med. 2016 Sep;45(8):599-604. doi: 10.1111/jop.12421. Epub 2016 Jan 29.
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Odontogenic Mixoma in a Ten-Year-Old Patient.一名10岁患者的牙源性混合瘤。
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Children (Basel). 2025 Jan 28;12(2):158. doi: 10.3390/children12020158.
2
Sinonasal Myxoma in an Infant: Observations on Its Distinctiveness and a Discussion on Potential Reclassification As Infantile Intraosseous Myxoid Desmoid Fibromatosis.婴儿鼻窦黏液瘤:关于其独特性的观察以及关于作为婴儿骨内黏液样硬纤维瘤病进行潜在重新分类的讨论。
Cureus. 2024 Aug 1;16(8):e65933. doi: 10.7759/cureus.65933. eCollection 2024 Aug.
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Sinonasal Myxoma: A Distinct Lesion of Infants.
鼻窦黏液瘤:一种婴儿的独特病变。
Head Neck Pathol. 2020 Mar;14(1):212-219. doi: 10.1007/s12105-018-0989-0. Epub 2018 Nov 27.
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Odontogenic Myxoma in Children: A Case Report and Literature Review.儿童牙源性黏液瘤:一例报告及文献复习
Case Rep Oncol Med. 2016;2016:9017421. doi: 10.1155/2016/9017421. Epub 2016 Mar 15.
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An unusual odontogenic myxoma in mandible and submandibular region: a rare case report.下颌骨及下颌下区罕见牙源性黏液瘤:1例罕见病例报告
Dentomaxillofac Radiol. 2014;43(8):20140087. doi: 10.1259/dmfr.20140087. Epub 2014 Oct 1.