一例罕见的眼眶恶性潜能不确定的血管球瘤伴BRAF致癌突变的年轻女性。

IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY
Sathyakumar Rima, Rangasamy Thiruvengadam Rajeswarie, Saritha Aryan, Prashant Alle
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引用次数: 0

摘要

21岁女性,右眼进行性突出,视力模糊6个月。MRI显示眼眶内病变T1等强度,T2高强度,对比增强良好。患者行右额叶开颅、上眶开颅和病变减压术。组织病理学显示血管球瘤伴有丝分裂增加,符合不确定恶性潜能的血管球瘤(GT-UMP)。GT-UMP具有侵袭性,需要在手术切除后进行辅助治疗。这些病例的BRAF V600E突变为靶向治疗和精准医学开辟了新的途径。这是第二例报道的涉及眼眶的GT-UMP病例,我们在该病例中证实了BRAF V600E突变,该突变在短时间内复发,重申了肿瘤的侵袭性和靶向治疗的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case of glomus tumor of uncertain malignant potential of orbit with BRAF oncogenic mutation in a young female.

A 21-year-old woman presented with progressive proptosis of the right eye with blurring of vision for the past 6 months. MRI showed an intra-orbital lesion that was T1 isointense, T2 hyperintense, and well enhancing on contrast. The patient underwent right frontal craniotomy, superior orbitotomy, and decompression of the lesion. Histopathology showed a glomus tumor with increased mitotic figures, consistent with a glomus tumor of uncertain malignant potential (GT-UMP). GT-UMP has an aggressive behavior that requires the need for adjuvant therapy following surgical excision. BRAF V600E mutation in these cases opens a new avenue for targeted therapy and precision medicine. This is the second reported case of a GT-UMP involving the orbit, and we have demonstrated BRAF V600E mutation in this case, which recurred in a short span, reiterating the aggressive nature of the tumor and the necessity of targeted therapy.

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来源期刊
Clinical Neuropathology
Clinical Neuropathology 医学-病理学
CiteScore
1.60
自引率
0.00%
发文量
70
审稿时长
>12 weeks
期刊介绍: Clinical Neuropathology appears bi-monthly and publishes reviews and editorials, original papers, short communications and reports on recent advances in the entire field of clinical neuropathology. Papers on experimental neuropathologic subjects are accepted if they bear a close relationship to human diseases. Correspondence (letters to the editors) and current information including book announcements will also be published.
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