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眼球摘除术后七年,葡萄膜黑色素瘤局部复发并伴有激活的端粒酶启动子突变相关的脑转移。

Local recurrence of uveal melanoma and concomitant brain metastases associated with an activating telomerase promoter mutation seven years after secondary enucleation.

作者信息

Heng Jacob S, Perzia Brittany M, Sinard John H, Pointdujour-Lim Renelle

机构信息

Department of Ophthalmology and Visual Science, Yale School of Medicine, 40 Temple Street Suite 3D, New Haven, CT, 06510, USA.

Department of Pathology, Yale School of Medicine, 20 York Street, CT, 06510, USA.

出版信息

Am J Ophthalmol Case Rep. 2022 Jun 1;27:101607. doi: 10.1016/j.ajoc.2022.101607. eCollection 2022 Sep.

Abstract

PURPOSE

To describe a case of local recurrence of uveal melanoma with concomitant brain metastases after secondary enucleation.

OBSERVATIONS

A 73 year-old patient presented with dizziness and gait instability. MRI of the orbits and brain showed an anophthalmic socket with an orbital implant and an associated optic nerve mass as well as multiple mass lesions in the brain. The patient's history was significant for secondary enucleation for uveal melanoma recurrence seven years prior to presentation. Histopathology of the enucleated eye revealed no signs of extrascleral extension or optic nerve invasion. Biopsy of the optic nerve mass confirmed recurrent uveal melanoma with somatic mutations in GNAQ (Q209L) and the telomerase (TERT) promoter (c.1-124C > T) found on targeted next-generation sequencing (NGS). The same mutations were found in the primary tumor in the patient's archived enucleation samples.

CONCLUSIONS

Local recurrence of uveal melanoma can occur after enucleation and is associated with an increased risk of systemic metastases. It is important for clinicians to monitor patients for local recurrence and systemic metastases even after enucleation. Genetic biomarkers may play an important role in identifying tumors at highest risk of local recurrence and metastasis. To our knowledge, this is the first case study to describe the TERT promoter mutation c.1-124C > T in the setting of recurrent uveal melanoma.

摘要

目的

描述1例眼球摘除术后葡萄膜黑色素瘤局部复发并伴有脑转移的病例。

观察结果

一名73岁患者出现头晕和步态不稳。眼眶和脑部的MRI显示无眼球眼眶内有一个眼眶植入物及相关视神经肿块,以及脑部多个肿块病变。该患者有7年前因葡萄膜黑色素瘤复发而进行眼球摘除术的病史。摘除眼球的组织病理学检查未发现巩膜外扩展或视神经侵犯的迹象。对视神经肿块进行活检,证实为复发性葡萄膜黑色素瘤,在靶向二代测序(NGS)中发现GNAQ(Q209L)和端粒酶(TERT)启动子(c.1-124C>T)存在体细胞突变。在患者存档的眼球摘除样本中的原发性肿瘤中也发现了相同的突变。

结论

葡萄膜黑色素瘤在眼球摘除术后可发生局部复发,并伴有全身转移风险增加。即使在眼球摘除术后,临床医生对患者进行局部复发和全身转移的监测也很重要。基因生物标志物可能在识别局部复发和转移风险最高的肿瘤方面发挥重要作用。据我们所知,这是首例描述复发性葡萄膜黑色素瘤中TERT启动子突变c.1-124C>T的病例研究。

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