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一例基底细胞型成釉细胞瘤的罕见病例报告及文献详细综述。

An unusual case report of basal cell ameloblastoma and a detailed review of literature.

作者信息

Buva Kirti, Deshmukh Ajinkya, Kavle Pratibha, Gupta Anish

机构信息

Oral Pathology and Microbiology, Bharati Vidyapeeth (Deemed to be University) Pune, Navi Mumbai, Maharashtra, India.

Oral Pathology and Microbiology, Preclinical Research Centre, Navi Mumbai, Maharashtra, India.

出版信息

J Oral Maxillofac Pathol. 2022 Apr-Jun;26(2):291. doi: 10.4103/jomfp.jomfp_95_22. Epub 2022 Jun 28.

DOI:10.4103/jomfp.jomfp_95_22
PMID:35968186
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9364650/
Abstract

Ameloblastoma is an odontogenic tumour derived from the remnants of odontogenic epithelium. Ameloblastoma shows versatile clinical and histological variants. Basal cell ameloblastoma is a rare variant among all histopathological variants of ameloblastoma. We present a case of a 25-year-old male patient with painless swelling on the lower left side of the face for 1 year, which had gradually increased in size and histologically showed features of basal cell ameloblastoma. The aim of the present paper is to understand this rare variant of ameloblastoma and review the literature.

摘要

成釉细胞瘤是一种源自牙源性上皮残余的牙源性肿瘤。成釉细胞瘤表现出多种临床和组织学变异型。基底细胞型成釉细胞瘤是成釉细胞瘤所有组织病理学变异型中的一种罕见类型。我们报告一例25岁男性患者，其左脸下部无痛性肿胀1年，肿物逐渐增大，组织学表现为基底细胞型成釉细胞瘤的特征。本文旨在了解这种罕见的成釉细胞瘤变异型并复习相关文献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/398ca136b948/JOMFP-26-291-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/ec5e3b7de7bb/JOMFP-26-291-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/2c705d80d0ca/JOMFP-26-291-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/25a47418ec2f/JOMFP-26-291-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/b9d62eb46ba3/JOMFP-26-291-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/9cf2fe94da18/JOMFP-26-291-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/57565ca8b230/JOMFP-26-291-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/398ca136b948/JOMFP-26-291-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/ec5e3b7de7bb/JOMFP-26-291-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/2c705d80d0ca/JOMFP-26-291-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/25a47418ec2f/JOMFP-26-291-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/b9d62eb46ba3/JOMFP-26-291-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/9cf2fe94da18/JOMFP-26-291-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/57565ca8b230/JOMFP-26-291-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8252/9364650/398ca136b948/JOMFP-26-291-g007.jpg

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本文引用的文献

1
Ameloblastic carcinoma ex ameloblastoma of the maxilla.上颌骨成釉细胞瘤恶变的成釉细胞癌。
J Oral Maxillofac Pathol. 2019 Feb;23(Suppl 1):58-62. doi: 10.4103/jomfp.JOMFP_116_17.
2
Clinicopathologic study on a rare variant of ameloblastoma with basal cell features.具有基底细胞特征的罕见成釉细胞瘤变体的临床病理研究。
Oral Dis. 2019 Apr;25(3):788-795. doi: 10.1111/odi.13018. Epub 2019 Jan 25.
3
Ameloblastoma-Clinical, radiological, and therapeutic findings.成釉细胞瘤—临床、放射学和治疗学表现。
Oral Dis. 2018 Mar;24(1-2):63-66. doi: 10.1111/odi.12702.
4
Unicystic ameloblastoma in conjunction with peripheral ameloblastoma: A unique case report presenting with diverse histological patterns.单囊性成釉细胞瘤合并外周型成釉细胞瘤：一例呈现多种组织学模式的独特病例报告。
J Oral Maxillofac Pathol. 2017 May-Aug;21(2):267-272. doi: 10.4103/jomfp.JOMFP_115_15.
5
Basal cell ameloblastoma: a rare histological variant of an uncommon tumor.基底细胞型成釉细胞瘤：一种罕见肿瘤的罕见组织学变异型。
Niger J Surg. 2015 Jan-Jun;21(1):66-9. doi: 10.4103/1117-6806.152730.
6
Basal cell ameloblastoma-review of literature with report of three cases.基底细胞型成釉细胞瘤——文献综述并附三例报告
J Oral Biol Craniofac Res. 2012 Jan-Apr;2(1):53-6. doi: 10.1016/S2212-4268(12)60013-X.
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Establishing the natural history and growth rate of ameloblastoma with implications for management: systematic review and meta-analysis.确定成釉细胞瘤的自然病史和生长速率及其对治疗的影响：系统评价和荟萃分析
PLoS One. 2015 Feb 23;10(2):e0117241. doi: 10.1371/journal.pone.0117241. eCollection 2015.
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Basal cell ameloblastoma of mandible: a rare case report with review.下颌骨基底细胞型成釉细胞瘤：1例罕见病例报告并文献复习
Case Rep Dent. 2013;2013:187820. doi: 10.1155/2013/187820. Epub 2013 Apr 8.
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Clinicopathological analysis of histological variants of ameloblastoma in a suburban Nigerian population.尼日利亚郊区人群成釉细胞瘤组织学变异型的临床病理分析
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Ameloblastoma: a surgeon's dilemma.成釉细胞瘤：外科医生的两难困境。
J Oral Maxillofac Surg. 2006 Jul;64(7):1010-4. doi: 10.1016/j.joms.2006.03.022.