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巨大甲状腺纤维肉瘤——病例报告

Giant Thyroid Fibrosarcoma- A Case Report.

作者信息

Tucciarone Manuel, Heredia-Llinas Carlos, Lowy-Benoliel Alejandro, Souviron-Encabo Rosalia, Martínez-Guirado Tomas, Álvarez-Morujo Ricardo González-Orus

机构信息

Department of Otorhinolaryngology, Gregorio Marañón Hospital, Madrid, SPAIN.

出版信息

Iran J Otorhinolaryngol. 2020 Mar;32(109):109-112. doi: 10.22038/ijorl.2019.39741.2310.

DOI:10.22038/ijorl.2019.39741.2310
PMID:32219077
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7085927/
Abstract

INTRODUCTION

Thyroid gland fibrosarcomas are extremely rare tumors, and only very few cases have been described in the literature. There are no set recommendations along with follow-ups regarding the treatment of these tumors. Moreover, the prognosis is poor with a very short life expectancy.

CASE REPORT

We present an 81-year-old patient who was suffering from increasing dysphagia and dysphonia related to a painless giant cervical mass, which presented with progressive growth for the preceding months. After a core needle biopsy with a suspicion of a solitary fibrous tumor, total excision of the tumor was successfully performed, and the pathology examination revealed a fibrosarcoma. Following surgery, radiotherapy was decided in the oncological multidisciplinary meeting; however, the patient refused it. There were neither new clinical symptoms nor tumor recurrence after an 18-month follow-up.

CONCLUSION

Although it is a very rare tumor, primary fibrosarcoma of the thyroid gland should be kept in mind in the differential diagnosis of neck tumors.

摘要

引言

甲状腺纤维肉瘤是极其罕见的肿瘤,文献中仅描述了极少数病例。对于这些肿瘤的治疗,没有既定的建议以及随访方案。此外,预后很差,预期寿命很短。

病例报告

我们报告一例81岁患者,因无痛性巨大颈部肿块出现吞咽困难和发音困难加重,该肿块在之前几个月呈进行性生长。在怀疑为孤立性纤维瘤进行粗针活检后,成功进行了肿瘤全切,病理检查显示为纤维肉瘤。手术后,在肿瘤多学科会议上决定进行放疗;然而,患者拒绝了。18个月的随访后既没有新的临床症状,也没有肿瘤复发。

结论

尽管是非常罕见的肿瘤,但在颈部肿瘤的鉴别诊断中应考虑到原发性甲状腺纤维肉瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fc6/7085927/cbed6850c8c7/ijo-32-109-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fc6/7085927/4f601c66487b/ijo-32-109-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fc6/7085927/b7f63a5cf044/ijo-32-109-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fc6/7085927/3c9dff0b3e9e/ijo-32-109-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fc6/7085927/cbed6850c8c7/ijo-32-109-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fc6/7085927/4f601c66487b/ijo-32-109-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fc6/7085927/b7f63a5cf044/ijo-32-109-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fc6/7085927/3c9dff0b3e9e/ijo-32-109-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fc6/7085927/cbed6850c8c7/ijo-32-109-g004.jpg

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Primary Thyroid Sarcoma: A Systematic Review.原发性甲状腺肉瘤:一项系统综述。
Anticancer Res. 2015 Oct;35(10):5185-91.
3
Prevalence and types of thyroid malignancies among thyroid enlarged patients in Gondar, Northwest Ethiopia: a three years institution based retrospective study.埃塞俄比亚西北部贡德尔甲状腺肿大患者中甲状腺恶性肿瘤的患病率及类型:一项基于机构的三年回顾性研究
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Thyroid Res. 2024 Mar 4;17(1):6. doi: 10.1186/s13044-023-00189-x.
BMC Cancer. 2014 Dec 2;14:899. doi: 10.1186/1471-2407-14-899.
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Myxofibrosarcoma of the thyroid gland.甲状腺黏液纤维肉瘤
Eur Ann Otorhinolaryngol Head Neck Dis. 2014 Dec;131(6):385-387. doi: 10.1016/j.anorl.2013.09.004. Epub 2014 Apr 1.
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