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14例牙源性黏液瘤的临床病理分析及文献复习

Clinicopathologic analysis of 14 cases of odontogenic myxoma and review of the literature.

作者信息

Francisco Ana-Lucia-Noronha, Chulam Thiago-Celestino, Silva Fábio-Oliveira, Ribeiro Diogo-Gonçalves, Pinto Clóvis-Antônio-Lopes, Gondak Rogério-Oliveira, Kowalski Luiz-Paulo, Gonçalves-Filho João

机构信息

DDS, PhD, Department of Head and Neck Surgery and Otorhinolaryngology, A.C. Camargo Cancer Center, São Paulo, Brazil.

MD, PhD, Department of Head and Neck Surgery and Otorhinolaryngology, A.C. Camargo Cancer Center, São Paulo, Brazil.

出版信息

J Clin Exp Dent. 2017 Apr 1;9(4):e560-e563. doi: 10.4317/jced.52953. eCollection 2017 Apr.

Abstract

BACKGROUND

Odontogenic myxoma is a rare benign neoplasm that originates from odontogenic ectomesenchyme. There is no standard of care and recurrences are frequent after conservative surgical procedures.

MATERIAL AND METHODS

A retrospective study conducted at a single cancer center, with analysis of medical records of all patients diagnosed with odontogenic myxoma from 1980 to 2010, along with a literature review.

RESULTS

There were 14 patients with diagnosis of odontogenic myxoma (OM). Most patients were female (78.6%) and Caucasian (100%), with ages ranging from 7 to 51 years (21.6 ± 11.6 years). The time period between the first symptom and first consultation ranged from 0 to 60 months (19.4 ± 19.97 months). The most frequent complaints were increased local volume or failure to tooth eruption. The most common tumor site was the mandible (11 cases, 78.5%). About radiological findings, most lesions were multilocular (9 cases, 64.3%) and with imprecise limits (12 cases, 85.7%). Surgery was performed in all cases and curettage was the most applied technique (10 cases, 71.4%). Three patients underwent mandibulectomy and complex reconstructions including iliac crest microvascular flap. Three patients had postoperative complications and 4 had local recurrences of the tumor. The follow up time ranged from 12 to 216 months (112 ± 70.8 months). All patients are without clinical and radiographic evidence of disease.

CONCLUSIONS

OM is a locally aggressive and rare tumor. There is no gold standard surgical management and the therapeutic decision should be individualized taking into account the characteristics and extension of the tumor. Mandible, myxoma, odontogenic, odontogenic tumor.

摘要

背景

牙源性黏液瘤是一种罕见的良性肿瘤,起源于牙源性外胚间叶组织。目前尚无标准的治疗方案,保守性手术治疗后复发频繁。

材料与方法

在单一癌症中心进行一项回顾性研究,分析1980年至2010年期间所有诊断为牙源性黏液瘤患者的病历,并进行文献综述。

结果

共有14例诊断为牙源性黏液瘤(OM)的患者。大多数患者为女性(78.6%),均为白种人(100%),年龄范围为7至51岁(21.6±11.6岁)。首发症状至首次就诊的时间间隔为0至60个月(19.4±19.97个月)。最常见的主诉是局部肿物增大或牙齿未萌出。最常见的肿瘤部位是下颌骨(11例,78.5%)。关于影像学表现,大多数病变为多房性(9例,64.3%)且边界不清(12例,85.7%)。所有病例均行手术治疗,刮除术是最常用的技术(10例,71.4%)。3例患者接受了下颌骨切除术及包括髂嵴微血管皮瓣在内的复杂重建手术。3例患者出现术后并发症,4例肿瘤局部复发。随访时间为12至216个月(112±70.8个月)。所有患者均无疾病的临床及影像学证据。

结论

牙源性黏液瘤是一种局部侵袭性罕见肿瘤。目前尚无金标准的手术治疗方法,治疗决策应根据肿瘤的特征和范围进行个体化考虑。下颌骨、黏液瘤、牙源性、牙源性肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/668d/5410678/eb1e37287f17/jced-9-e560-g001.jpg

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