Mid and South Essex NHS Foundation Trust, Broomfield Hospital, Department of Otolaryngology, Chelmsford, Essex, CM1 7ET, United Kingdom.
Mid and South Essex NHS Foundation Trust, Broomfield Hospital, Department of Otolaryngology, Chelmsford, Essex, CM1 7ET, United Kingdom.
Braz J Otorhinolaryngol. 2022 Nov-Dec;88 Suppl 4(Suppl 4):S177-S187. doi: 10.1016/j.bjorl.2022.04.002. Epub 2022 May 20.
Due to the rarity of osteolipoma, current knowledge and understanding of its' clinical presentation, management, radiological features, histological characteristics, and prognosis are lacking and can present a clinical conundrum to clinicians and histopathologist alike, given wide range of differential diagnoses. This paper aims to compile, analyse and present details to augment the available literature on osteolipoma in the head and neck.
A comprehensive literature search on PUBMED/MEDLINE, EMBASE, CINAHL and Science Citation Index, Google scholar and Cochrane database for osteolipoma in head and neck was performed up to the 1st May 2021. Reference lists from the relevant articles were then inspected and cross-referenced and any other pertinent publications were added to the review.
A total of 38 cases were identified from the literature. The commonest sites of involvement within the head and neck region were the oral cavity in 21 (56.8%) patients, followed by the neck in 7 (19.0%) patients. 29 (78.4%) patients presented with soft tissue swelling or mass making it the most common presenting feature. All patients had the tumour excised surgically; of which 18 (48.6%) were excised via transoral approach and 6 (16.2%) via open transcervical approach including 1 lateral pharyngotomy. 12 papers documented long-term follow-ups (median 12 months) with no recurrence. Only 1 regrowth was reported after 5-years.
Osteolipoma is a rare soft tissue neoplasm which has a wide range differential diagnosis including malignant processes. Recognising this benign tumour through an awareness of presenting sign and symptoms, radiological features and histopathology findings is important for patient reassurance as well as avoiding unnecessary radical treatment.
由于骨脂瘤罕见,目前对其临床表现、治疗、影像学特征、组织学特征和预后的认识有限,由于广泛的鉴别诊断,这可能给临床医生和组织病理学家带来临床难题。本文旨在收集、分析和提供详细信息,以增加有关头颈部骨脂瘤的现有文献。
对 PUBMED/MEDLINE、EMBASE、CINAHL 和科学引文索引、Google 学术和 Cochrane 数据库进行了全面的文献检索,以查找头颈部骨脂瘤的文献,检索时间截至 2021 年 5 月 1 日。然后检查和交叉引用相关文章的参考文献,并添加任何其他相关出版物进行综述。
从文献中总共确定了 38 例病例。头颈部最常见的受累部位是口腔,21 例(56.8%)患者,其次是颈部 7 例(19.0%)患者。29 例(78.4%)患者表现为软组织肿胀或肿块,这是最常见的表现特征。所有患者均通过手术切除肿瘤;其中 18 例(48.6%)通过经口入路切除,6 例(16.2%)通过开放式经颈入路切除,包括 1 例侧咽切开术。12 篇文献记录了长期随访(中位数 12 个月),无复发。仅 1 例在 5 年后报告复发。
骨脂瘤是一种罕见的软组织肿瘤,其鉴别诊断范围广泛,包括恶性肿瘤。通过对临床表现、影像学特征和组织病理学发现的认识,认识到这种良性肿瘤对患者的安心以及避免不必要的激进治疗非常重要。