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下颌骨角化成釉细胞瘤:一种罕见的具有挑战性的病变。

Keratoameloblastoma of the lower jaw: A rare challenging entity.

作者信息

Moradi Mina, Neville Brad W, Aminishakib Pouyan

机构信息

Department of Oral and Maxillofacial Pathology, Tehran University of Medical Sciences, Tehran, Iran.

HCA South Atlantic Division, Trident Medical Center, Charleston, South Carolina, USA.

出版信息

Dent Res J (Isfahan). 2023 Jul 25;20:77. eCollection 2023.

PMID:37674569
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10478832/
Abstract

Ameloblastoma is the second most common benign odontogenic tumor with various histopathologic features. Except for the unicystic type of ameloblastoma, the different microscopic patterns of this tumor show no significant correlation with long-term clinical behavior. During recent decades, additional challenging subtypes of ameloblastoma, including "Keratoameloblastoma" (KA), have been introduced in the literature. Here, we present a case of KA and discuss the important diagnostic microscopic features.

摘要

成釉细胞瘤是第二常见的具有多种组织病理学特征的良性牙源性肿瘤。除单囊性成釉细胞瘤外,该肿瘤的不同微观模式与长期临床行为无显著相关性。在最近几十年中,文献中引入了成釉细胞瘤的其他具有挑战性的亚型,包括“角化成釉细胞瘤”(KA)。在此,我们报告一例KA病例并讨论重要的诊断微观特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9688/10478832/e8ab0d3a1e20/DRJ-20-77-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9688/10478832/6133bb13cce2/DRJ-20-77-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9688/10478832/e8ab0d3a1e20/DRJ-20-77-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9688/10478832/6133bb13cce2/DRJ-20-77-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9688/10478832/e8ab0d3a1e20/DRJ-20-77-g002.jpg

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1
Keratoameloblastoma of the lower jaw: A rare challenging entity.下颌骨角化成釉细胞瘤:一种罕见的具有挑战性的病变。
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本文引用的文献

1
Keratoameloblastoma: A Report of Seven New Cases and Review of Literature.角化性成釉细胞瘤:七例新病例报告及文献复习。
Head Neck Pathol. 2022 Dec;16(4):1103-1113. doi: 10.1007/s12105-022-01470-5. Epub 2022 Jul 21.
2
Papilliferous keratoameloblastoma - A rare entity: A case report with a review of literature.乳头状角化性成釉细胞瘤——一种罕见的实体:一例病例报告并文献复习
J Oral Maxillofac Pathol. 2020 Feb;24(Suppl 1):S2-S6. doi: 10.4103/jomfp.JOMFP_42_17. Epub 2020 Feb 28.
3
Papilliferous Keratoameloblastoma of the Mandible - A Rare Case Report.
下颌骨乳头状角化囊性瘤——1例罕见病例报告
J Clin Diagn Res. 2016 Aug;10(8):ZD08-11. doi: 10.7860/JCDR/2016/18862.8232. Epub 2016 Aug 1.
4
Keratoameloblastoma or Kerato-odontoameloblastoma: report of its soft tissue recurrence with literature review.角化成釉细胞瘤或角化牙源性成釉细胞瘤:软组织复发报告及文献复习
Quant Imaging Med Surg. 2015 Dec;5(6):898-908. doi: 10.3978/j.issn.2223-4292.2015.09.01.
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Keratoameloblastoma: a case report and a review of the literature on its radiologic features.角化性成釉细胞瘤:一例病例报告及关于其放射学特征的文献综述
Oral Surg Oral Med Oral Pathol Oral Radiol. 2015 Nov;120(5):e219-25. doi: 10.1016/j.oooo.2015.07.008. Epub 2015 Jul 22.
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Keratoameloblastoma a rare entity: a case report.角化性成釉细胞瘤:一种罕见的病变——病例报告
J Clin Diagn Res. 2015 Mar;9(3):ZD05-7. doi: 10.7860/JCDR/2015/10111.5637. Epub 2015 Mar 1.
7
Keratoameloblastoma: Report of a rare variant with review of literature.角化成釉细胞瘤:一种罕见变异型的病例报告及文献复习
Dent Res J (Isfahan). 2014 Sep;11(5):610-4.
8
Keratoameloblastoma, a very rare variant of ameloblastoma.角化成釉细胞瘤,成釉细胞瘤的一种非常罕见的变体。
J Craniofac Surg. 2013 Nov;24(6):2182-6. doi: 10.1097/SCS.0b013e3182a28be3.
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Papilliferous keratoameloblastoma: an extremely rare case report.
Case Rep Dent. 2013;2013:706128. doi: 10.1155/2013/706128. Epub 2013 Jun 3.
10
Surgical management of ameloblastoma: Conservative or radical approach.成釉细胞瘤的外科治疗:保守还是根治方法。
Natl J Maxillofac Surg. 2011 Jan;2(1):22-7. doi: 10.4103/0975-5950.85849.