Primary osteosarcoma of the jaw: clinicopathological characterization of a rare tumour

Diagnostic Histopathology Pub Date : 2026-10-01 Epub Date: 2026-08-14 DOI:10.1016/j.mpdhp.2026.07.009
Sarah Ruane, Guy Betts
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引用次数: 0

Abstract

Osteosarcomas are the most common primary bone malignancy, typically affecting the long bones. Rarely are they found within the jaw, but when they do so, they present with paraesthesia, swelling and tooth loss. Herein we present a case of primary osteosarcoma of the mandible in a 76-year-old man, similarly, presenting to clinicians with paraesthesia, jaw swelling and loss of his back molar tooth. Computed tomography (CT) showed a spiculated lesion arising from bone, with overlying soft tissue infiltration, confirmed by Histopathology as a high-grade osteoblastic osteosarcoma. The patient underwent a hemi-mandibulectomy and lymph node dissection, with reconstructive surgery. A focused literature view highlights the; presentation, investigation, and management of jaw osteosarcomas, and touches on how immunohistochemical and genetic factors are hoping to effectively aid in the treatment and prognostication of patients, ultimately aiming to provide a more personalised and precision-based care for this rare entity.
颌骨原发性骨肉瘤:一种罕见肿瘤的临床病理特征
骨肉瘤是最常见的原发性骨恶性肿瘤,通常影响长骨。很少在颌骨内发现,但当他们这样做时,他们表现为感觉异常,肿胀和牙齿脱落。在此,我们提出一个76岁男性下颌骨原发性骨肉瘤的病例,同样,向临床医生提出感觉异常,下颌肿胀和失去他的后磨牙。计算机断层扫描(CT)显示骨产生的刺状病变,伴有软组织浸润,组织病理学证实为高级别成骨细胞骨肉瘤。患者接受了半下颌切除术和淋巴结清扫,并进行了重建手术。一个集中的文学观点突出;颌骨骨肉瘤的表现、调查和管理,并触及免疫组织化学和遗传因素如何希望有效地帮助患者的治疗和预后,最终旨在为这种罕见的实体提供更个性化和精确的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Diagnostic Histopathology
Diagnostic Histopathology Medicine-Pathology and Forensic Medicine
CiteScore
1.30
自引率
0.00%
发文量
64
期刊介绍: This monthly review journal aims to provide the practising diagnostic pathologist and trainee pathologist with up-to-date reviews on histopathology and cytology and related technical advances. Each issue contains invited articles on a variety of topics from experts in the field and includes a mini-symposium exploring one subject in greater depth. Articles consist of system-based, disease-based reviews and advances in technology. They update the readers on day-to-day diagnostic work and keep them informed of important new developments. An additional feature is the short section devoted to hypotheses; these have been refereed. There is also a correspondence section.
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