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舌骨软骨肉瘤:影像学、手术及组织病理学相关性

Chondrosarcoma of the hyoid bone: imaging, surgical, and histopathologic correlation.

作者信息

Saki Nader, Akhlagh Soheila Nik, Mostofi Neptone Emad, Ahmadi Khashayar

机构信息

Department of Otolaryngology-Head and Neck Surgery, Imam Khomeini Hospital, Ahwaz Jondishapour University of Medical Sciences, Iran.

出版信息

Laryngoscope. 2008 Jul;118(7):1211-3. doi: 10.1097/MLG.0b013e318170f8bd.

Abstract

OBJECTIVES/HYPOTHESIS: Rare diseases must be diagnosed with great caution, so we present this case to familiarize clinicians with the presentation and treatment of chondrosarcoma of the hyoid bone, a rare disease.

STUDY DESIGN

Case report and review of the literature.

METHODS

We report one case of chondrosarcoma of the hyoid bone which presented with upper midline neck mass. In addition, we review the literature published in English regarding chondrosarcoma of the hyoid bone.

RESULTS

Chondrosarcoma of the hyoid bone is a rare disease of which only 14 cases have been reported until now. Patients with this disease have no sexual or racial preponderance, and most presented with a mass in the upper neck which has splotchy calcification in radiologic imaging without enhancement. The preferred treatment is wide excision.

CONCLUSION

Because chondrosarcoma have indolent growth, are locally noninvasive, and appear encapsulated during operation, they may be mistaken for a benign mass and conservatively resected. On the other hand, incomplete tumor resection may lead to recurrence, which is associated with increased risk of dedifferentiation and histologic grading of tumor. Surgeons should approach this surgery with caution.

摘要

目的/假设:罕见疾病的诊断必须极其谨慎,因此我们呈现此病例,以使临床医生熟悉舌骨软骨肉瘤这种罕见疾病的表现及治疗方法。

研究设计

病例报告及文献综述。

方法

我们报告1例以颈部中线中上段肿块为表现的舌骨软骨肉瘤病例。此外,我们回顾了以英文发表的有关舌骨软骨肉瘤的文献。

结果

舌骨软骨肉瘤是一种罕见疾病,目前仅有14例报道。该疾病患者无性别或种族倾向,大多数患者表现为上颈部肿块,影像学检查可见斑点状钙化且无强化。首选治疗方法是广泛切除。

结论

由于软骨肉瘤生长缓慢、局部无侵袭性且在手术中看似有包膜,它们可能被误诊为良性肿块并接受保守切除。另一方面,肿瘤切除不完全可能导致复发,这与去分化风险增加及肿瘤组织学分级相关。外科医生应谨慎进行此类手术。

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