下颌骨前部动脉瘤性骨囊肿

IF 3.2 Q2 PATHOLOGY
Sinval Vinícius Barbosa do Nascimento, Weslay Rodrigues da Silva, Caroline Augusta Belo Faria, Roberta Karolina Borges de Souza, Carlos Augusto Pereira do Lago, Ana Paula Veras Sobral
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引用次数: 0

摘要

动脉瘤性骨囊肿是一种罕见的溶骨性病变,病因不明,常见于下肢,仅有1%-2%的病例报告发生在颌骨。本病例是一名 27 岁的男性患者,因主诉精神区域麻痹和下颌骨体积增大而转诊至口腔颌面外科和创伤科。体格检查显示其中线移位和硬结。影像学检查显示下颌骨皮质有放射性/高密度病变。切口活检组织病理学检查诊断为中央巨细胞病变。患者接受了手术切除,标本的组织病理学分析显示,病变主要为实性,其特征为大小不等的充血空隙,未被上皮或内皮覆盖,存在纺锤形细胞、多核巨细胞和嗜碱性骨物质,最终诊断为混合型动脉瘤性骨囊肿。尽管动脉瘤性骨囊肿并不常见,但在年轻患者颌骨体积增大的鉴别诊断中仍应考虑到它。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aneurysmal Bone Cyst in the Anterior Region of the Mandible.

Aneurysmal bone cyst is a rare osteolytic lesion of uncertain etiology, commonly observed in the lower limbs, with only 1-2% of reports in gnathic bones. We present the case of a 27-year-old male patient referred to the oral and maxillofacial surgery and traumatology service due to complaints of paresthesia in the mental region and increased mandibular volume. Physical examination revealed midline shift and hard consistency. Imaging examinations demonstrated a radiolucent/hypodense lesion with disruption of the mandibular cortices. The histopathological examination of incisional biopsy material led to the diagnosis of a central giant cell lesion. The patient underwent surgical resection, and the histopathological analysis of the specimen revealed a predominantly solid lesion, characterized by blood-filled spaces of varying size, not covered by epithelium or endothelium, with the presence of spindle cells, multinucleated giant cells, and basophilic osteoid material, concluding the diagnosis of mixed-type aneurysmal bone cyst. Despite being uncommon, aneurysmal bone cysts should be considered in the differential diagnosis of volumetric increase in the gnathic bones of young patients.

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来源期刊
CiteScore
5.70
自引率
9.50%
发文量
99
期刊介绍: Head & Neck Pathology presents scholarly papers, reviews and symposia that cover the spectrum of human surgical pathology within the anatomic zones of the oral cavity, sinonasal tract, larynx, hypopharynx, salivary gland, ear and temporal bone, and neck. The journal publishes rapid developments in new diagnostic criteria, intraoperative consultation, immunohistochemical studies, molecular techniques, genetic analyses, diagnostic aids, experimental pathology, cytology, radiographic imaging, and application of uniform terminology to allow practitioners to continue to maintain and expand their knowledge in the subspecialty of head and neck pathology. Coverage of practical application to daily clinical practice is supported with proceedings and symposia from international societies and academies devoted to this field. Single-blind peer review The journal follows a single-blind review procedure, where the reviewers are aware of the names and affiliations of the authors, but the reviewer reports provided to authors are anonymous. Single-blind peer review is the traditional model of peer review that many reviewers are comfortable with, and it facilitates a dispassionate critique of a manuscript.
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