Suppr超能文献

扁桃体滑膜肉瘤,不常见的解剖部位:病例报告及文献复习。

Tonsillar synovial sarcoma, unusual anatomical location: case report and literature review.

机构信息

Department of Pathology and Microbiology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, 22110, Jordan.

Department of Pathology and Microbiology, Faculty of Medicine, King Abdullah University Hospital, Jordan University of Science and Technology, Irbid, 22110, Jordan.

出版信息

Diagn Pathol. 2024 Jul 26;19(1):104. doi: 10.1186/s13000-024-01524-y.

Abstract

BACKGROUND

Synovial sarcoma is a rare soft tissue malignancy, occasionally found in the head and neck region. The diagnosis necessitates a multidisciplinary approach involving the clinical presentation, proper imaging studies and histological confirmation, with molecular testing for definitive identification. Treatment entails surgical resection with adjuvant therapies as needed.

CASE PRESENTATION

A 33-year-old male patient presented with globus sensation concomitant with right-sided neck swelling. He was clinically found to have right tonsil enlargement with posterior extension. Therefore, he underwent right tonsillectomy with pharyngoplasty. Histopathological examination revealed a biphasic tumor consistent with synovial sarcoma, confirmed by immunohistochemistry and fluorescence in situ hybridization.

CONCLUSIONS

Tonsillar synovial sarcoma represents a diagnostic challenge, requiring a high index of suspicion and comprehensive evaluation. With only twenty previously published cases documented in the literature, awareness of this rare presentation is crucial for prompt diagnosis and appropriate management. Collaboration among multidisciplinary healthcare teams and ongoing research efforts are essential for optimizing diagnostic accuracy, treatment efficacy, and patient outcomes in this rare malignancy.

摘要

背景

滑膜肉瘤是一种罕见的软组织恶性肿瘤,偶尔出现在头颈部。诊断需要多学科方法,包括临床表现、适当的影像学研究和组织学确认,并进行分子检测以明确诊断。治疗需要手术切除,并根据需要辅助治疗。

病例介绍

一名 33 岁男性患者出现咽部异物感伴右侧颈部肿胀。临床检查发现右侧扁桃体增大并向后延伸。因此,他接受了右侧扁桃体切除术和咽成形术。组织病理学检查显示为符合滑膜肉瘤的双相性肿瘤,免疫组织化学和荧光原位杂交进一步证实了这一诊断。

结论

扁桃体滑膜肉瘤是一种具有挑战性的诊断,需要高度怀疑和全面评估。文献中仅报道了 20 例先前的病例,因此,对这种罕见表现的认识对于及时诊断和适当治疗至关重要。多学科医疗团队的合作和持续的研究努力对于提高这种罕见恶性肿瘤的诊断准确性、治疗效果和患者预后至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47a8/11282668/e5396d45d593/13000_2024_1524_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验