Congenital intestinal fibrosarcoma with rapid recurrence requiring adjuvant chemotherapy
Publication in refereed journal

香港中文大學研究人員
替代計量分析
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其它資訊
摘要A total of 16 cases of congenital fibrosarcoma have been reported from 1975 to March 2015. Five of the 16 had abnormal fusion between erythroblast transformation specific translocation variant 6 and neurotrophin recptor gene neurotrophic tyrosine kinase, receptor, type 3 (ETV6-NTRK3); in another five out of 16 this was absent, and six were not tested. All were managed by surgical resection but none involved metastasis. Herein we report the case of a newborn baby girl with congenital fibrosarcoma negative for ETV6-NTRK3 gene fusion, who presented with ileal perforation and positive resection margin. She had rapid recurrence with lymph node metastasis treated with postoperative chemotherapy. There was no further recurrence at >3 years of follow up.
著者See WSQ, Cheuk DKL, To KF, Ip PPC, Chiang AKS, Ha SY, Chan GCF.
期刊名稱Pediatrics International
出版年份2017
月份6
卷號59
期次6
出版社Wiley
頁次733 - 736
國際標準期刊號1328-8067
語言英式英語
關鍵詞chemotherapy, congenital fibrosarcoma, intestinal, metastasis, rare tumor

上次更新時間 2021-01-03 於 01:29