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侧颅底低度恶性纤维黏液样肉瘤:2例病例报告

Low-Grade Fibromyxoid Sarcoma of the Lateral Skull Base: Presentation of Two Cases.

作者信息

Chetverikova Evgenia, Kasenõmm Priit

机构信息

Department of Otorhinolaryngology, Tartu University Hospital, J. Kuperjanovi 1, 51003 Tartu, Estonia.

Institute of Clinical Medicine, University of Tartu, L. Puusepa 8, 50406 Tartu, Estonia.

出版信息

Case Rep Otolaryngol. 2019 Jul 8;2019:7917040. doi: 10.1155/2019/7917040. eCollection 2019.

DOI:10.1155/2019/7917040
PMID:31360570
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6644311/
Abstract

Low-grade fibromyxoid sarcoma (LGFMS) is a rare slow-growing malignant tumour with a deceptively benign histologic appearance. Herein, we report two cases of LGFMS with variable clinical presentations. The first case was a 17-year-old female who referred to our department due to deaf ear on the right together with ipsilateral gag reflex impairment and globus sensation in the pharynx. The second case was a 35-year-old female with recurrent LGFMS, suffering from headaches, vertigo, and episodes of loss of consciousness. LGFMS of the temporal bone is a rare pathology, and to the best of our knowledge, no such cases have been reported before.

摘要

低度恶性纤维黏液样肉瘤(LGFMS)是一种罕见的生长缓慢的恶性肿瘤,其组织学表现看似良性。在此,我们报告两例临床表现各异的LGFMS病例。第一例为一名17岁女性,因右耳失聪、同侧咽反射障碍及咽部异物感前来我院就诊。第二例为一名35岁女性,患有复发性LGFMS,伴有头痛、眩晕及意识丧失发作。颞骨LGFMS是一种罕见的病理情况,据我们所知,此前尚无此类病例的报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a56/6644311/e42d4778c78e/CRIOT2019-7917040.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a56/6644311/df32107ae2a5/CRIOT2019-7917040.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a56/6644311/b80a76e3e25e/CRIOT2019-7917040.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a56/6644311/e42d4778c78e/CRIOT2019-7917040.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a56/6644311/df32107ae2a5/CRIOT2019-7917040.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a56/6644311/b80a76e3e25e/CRIOT2019-7917040.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a56/6644311/e42d4778c78e/CRIOT2019-7917040.003.jpg

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