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鼻窦纤维肉瘤:一项系统评价

Fibrosarcomas of the Paranasal Sinuses: A Systematic Review.

作者信息

Bughrara Moneb S, Almsaddi Tarek, John Jithin, Prentice Brandon, Johnson Jared, Henriquez Oswaldo, Folbe Adam J

机构信息

Internal Medicine, Oakland University William Beaumont School of Medicine, Rochester Hills, USA.

Otolaryngology, Oakland University William Beaumont School of Medicine, Rochester Hills, USA.

出版信息

Cureus. 2022 Aug 10;14(8):e27868. doi: 10.7759/cureus.27868. eCollection 2022 Aug.

Abstract

Fibrosarcomas are rare, malignant neoplasms of mesenchymal origin. Fibrosarcomas appear to be sporadic, but cases of fibrosarcomas secondary to radiation of nasopharyngeal carcinomas have been reported. Paranasal sinus fibrosarcomas (PNFS) are even rarer with few cases being reported since the 1950s. There have been several retrospective cohort studies examining PNFS; however, to our knowledge, no comprehensive review exists. This review aims to summarize the findings of all published cases of PNFS from the 1950s to the 2020s. We hope that a comprehensive review will assist in accurate and early diagnoses of PNFS, and help guide treatment as early treatment is associated with a favorable prognosis.This systematic review reports results following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A search was conducted on PubMed, Embase, and Cochrane Library. Studies were screened using established inclusion/exclusion criteria. A total of 26 studies were included for data extraction, and relevant data were collected and analyzed.In our study, the most common study type was case reports (n = 19). The most common presentation for PNFS included male gender (n = 17) with maxillary sinus (n = 57) involvement. Patients commonly presented with complaints of nasal obstruction (n = 15), epistaxis (n = 11), and facial fullness/pain (n = 9). Surgical resection was the mainstay treatment, with the use of chemotherapy or radiation depending on surgical margins and resectability. The diagnosis was commonly made with histological analysis. This review of the literature provides a summary and reference of important presenting factors, elements of diagnosis, and treatment options regarding PNFS to help bring awareness and guide the treatment of such a rare disease. Moving forward, there is a greater need for larger standardized studies that can further complement our findings, as well as more consistent reporting of cases.

摘要

纤维肉瘤是一种罕见的间叶组织起源的恶性肿瘤。纤维肉瘤似乎是散发性的,但也有继发于鼻咽癌放疗后的纤维肉瘤病例报道。鼻窦纤维肉瘤(PNFS)更为罕见,自20世纪50年代以来仅有少数病例报道。已有多项回顾性队列研究对PNFS进行了考察;然而,据我们所知,尚无全面的综述。本综述旨在总结20世纪50年代至21世纪20年代所有已发表的PNFS病例的研究结果。我们希望全面的综述将有助于PNFS的准确早期诊断,并有助于指导治疗,因为早期治疗与良好的预后相关。本系统综述按照系统评价和Meta分析的首选报告项目(PRISMA)指南报告结果。在PubMed、Embase和Cochrane图书馆进行了检索。使用既定的纳入/排除标准对研究进行筛选。共纳入26项研究进行数据提取,并收集和分析相关数据。在我们的研究中,最常见的研究类型是病例报告(n = 19)。PNFS最常见的表现包括男性(n = 17),累及上颌窦(n = 57)。患者常见的主诉包括鼻塞(n = 15)、鼻出血(n = 11)和面部饱满/疼痛(n = 9)。手术切除是主要的治疗方法,根据手术切缘和可切除性使用化疗或放疗。诊断通常通过组织学分析做出。本文献综述提供了关于PNFS的重要临床表现因素、诊断要素和治疗选择的总结和参考,以帮助提高对此类罕见疾病的认识并指导治疗。展望未来,更需要大规模的标准化研究来进一步补充我们的研究结果,以及更一致的病例报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d592/9462655/10838162531b/cureus-0014-00000027868-i01.jpg

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