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一名卵巢恶性间皮瘤患者中新型STRN-ALK与NBEA-ALK双融合的共存:病例报告与文献复习

Coexistence of a novel STRN-ALK, NBEA-ALK double-fusion in an ovarian malignant mesothelioma patient: a case report and review.

作者信息

Wu Xiao, Wang Qi, Xu Xiaohu

机构信息

Department of Integrated Traditional Chinese and Western Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Front Oncol. 2023 Apr 21;13:1156329. doi: 10.3389/fonc.2023.1156329. eCollection 2023.

Abstract

Primary ovarian mesothelioma (POM) is a rare malignant tumor with poor prognosis. Although anaplastic lymphoma kinase gene (ALK) double-fusion partners have been found in various tumors, it is rarely reported in mesothelioma. In this article, we describe the coexistence of a novel STRN-ALK, neurobeachin (NBEA)-ALK double-fusion in a patient with primary ovarian mesothelioma. A 30-year-old woman was found to have pelvic masses for more than a year. Color Doppler ultrasound showed mixed mass in the left ovary and multiple solid masses in the right ovary. the patient underwent laparoscopic surgery, including total hysterectomy, bilateral salpingo-oopherectomy, pelvic lymph node and abdominal aortic lymph node resection, omentum resection and abdominal focus resection. Pathologic examination revealed bilateral ovarian malignant mesothelioma and no evidence of malignancy in the resected bilateral round/broad ligaments, bilateral parametrial tissues, vaginal stump, bilateral fallopian tubes, pelvic and paraaortic lymph nodes. Immunohistochemistry showed that it was positive for Calretinin, VIM, WT1, PAX8, mesothelin, CK5/6, PCK, CK7, MLH1, PMS2, MSH2, MSH6, weakly positive for BAP1, while being negative for Napsin A, P504S, CEA, D2-40, GATA3. The sequencing analysis identified STRN-ALK (intron3:intron19) and NBEA-ALK (intron1:intron16) double-ALK fusion. To the best of our knowledge, this is the first report that a novel NBEA-ALK and EML4-ALK coexist in one patient with POM. The patient has completed 6 cycles of continuous chemotherapy and is in stable condition. Whether ALK inhibitors can bring promising benefits to POM patients in the future deserves further study.

摘要

原发性卵巢间皮瘤(POM)是一种罕见的恶性肿瘤,预后较差。尽管在各种肿瘤中已发现间变性淋巴瘤激酶基因(ALK)双融合伴侣,但在间皮瘤中鲜有报道。在本文中,我们描述了一名原发性卵巢间皮瘤患者中存在一种新型的STRN-ALK、神经海滩蛋白(NBEA)-ALK双融合。一名30岁女性被发现盆腔肿物一年多。彩色多普勒超声显示左卵巢混合性肿物,右卵巢多个实性肿物。患者接受了腹腔镜手术,包括全子宫切除术、双侧输卵管卵巢切除术、盆腔淋巴结和腹主动脉旁淋巴结切除术、大网膜切除术及腹部病灶切除术。病理检查显示双侧卵巢恶性间皮瘤,切除的双侧圆韧带/阔韧带、双侧宫旁组织、阴道残端、双侧输卵管、盆腔及腹主动脉旁淋巴结未见恶性证据。免疫组化显示Calretinin、VIM、WT1、PAX8、间皮素、CK5/6、PCK、CK7、MLH1、PMS2、MSH2、MSH6呈阳性,BAP1弱阳性,而Napsin A、P504S、CEA、D2-40、GATA3呈阴性。测序分析确定存在STRN-ALK(内含子3:内含子19)和NBEA-ALK(内含子1:内含子16)双ALK融合。据我们所知,这是首例关于新型NBEA-ALK和EML4-ALK在一名POM患者中共存的报道。该患者已完成6个周期的持续化疗,病情稳定。未来ALK抑制剂是否能给POM患者带来有前景的益处值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d7f/10160359/6c3154662784/fonc-13-1156329-g001.jpg

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