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下颌骨侵袭性多房性骨母细胞瘤:一例罕见且诊断困难的病例

Aggressive multilocular osteoblastoma in the mandible: a rare and difficult case to diagnose.

作者信息

Pontual Maria Luiza Anjos, Pontual Andréa Anjos, Grempel Rafael Grotta, Campos Leonardo Rocha Mendes, Costa Antonio de Lisboa Lopes, Godoy Gustavo Pina

机构信息

Department of Preventive and Clinical Dentistry, Health Science Center, UFPE - Universidade Federal de Pernambuco, Recife, PE, Brazil.

Unipê, João Pessoa, PB, Brazil.

出版信息

Braz Dent J. 2014 Sep-Oct;25(5):451-6. doi: 10.1590/0103-6440201300220.

Abstract

Osteoblastoma is a benign neoplasia and is uncommon in the jaws. In some cases, this lesion presents extremely aggressive local characteristics and is termed aggressive osteoblastoma. Because the clinical, radiographic and histopathologic characteristics are similar to those of a variety of benign and malignant tumors, it poses a diagnostic dilemma. This report presents a case of an aggressive osteoblastoma in the mandible and discusses the differential diagnosis of this lesion. A 13-year-old white male sought the Stomatology Clinic at the State University of Paraíba, Campina Grande, PB, Brazil, complaining of asymptomatic swelling on the left side of his face. Cone-beam computerized tomography showed a multilocular, hypodense bone lesion, located in the body of the left mandible and lower third of the ascending ramus. The initial diagnostic hypothesis was juvenile ossifying fibroma or osteosarcoma. After histopathologic examination, the final diagnosis was aggressive osteoblastoma. Surgical resection with a safety margin was performed. There was no evidence of recurrence after a follow-up period of 4 years.

摘要

骨母细胞瘤是一种良性肿瘤,在颌骨中并不常见。在某些情况下,这种病变具有极其侵袭性的局部特征,被称为侵袭性骨母细胞瘤。由于其临床、影像学和组织病理学特征与多种良性和恶性肿瘤相似,因此造成了诊断上的困境。本报告介绍了一例下颌骨侵袭性骨母细胞瘤病例,并讨论了该病变的鉴别诊断。一名13岁的白人男性前往巴西帕拉伊巴州立大学坎皮纳格兰德分校的口腔诊所就诊,主诉左侧面部无症状肿胀。锥形束计算机断层扫描显示一个多房性、低密度骨病变,位于左下颌骨体部和升支下三分之一处。最初的诊断假设是青少年骨化性纤维瘤或骨肉瘤。经过组织病理学检查,最终诊断为侵袭性骨母细胞瘤。进行了带安全切缘的手术切除。随访4年没有复发迹象。

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