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切除的十二指肠胃肠道间质瘤,切缘受侵且存在外显子 9 突变:辅助治疗。

Resected duodenal gastrointestinal stromal tumour with an affected margin and exon 9 mutation: adjuvant therapy.

机构信息

Medical Oncology Unit, La Paz Hospital bCIOCC, Madrid, Spain.

出版信息

Anticancer Drugs. 2012 Jun;23 Suppl:S18-21. doi: 10.1097/CAD.0b013e3283559fcd.

Abstract

We report on a 44-year-old female patient complaining of epigastric pain with an initial diagnosis of acute pancreatitis. Three months later, the symptoms reappeared and an abdomen computed tomography scan showed a mass in the third portion of the duodenum. After surgical resection, the pathologist confirmed malignant mesenchymal proliferation with a mitotic index of 2 mitoses/50 HPF. There was no tumour necrosis. The proliferation index (Ki 67) was 2%. A mutational analysis was carried out, which identified a mutation in c-KIT exon 9, with duplication of codons 502 and 503. A radical surgery was rejected by the patient and adjuvant therapy with imatinib at an initial dose of 400 mg/day was considered, with the intention of increasing the dose to 800 mg/day because of the presence of mutation in c-KIT exon 9 related to a poor response to imatinib. However, because of the adverse effects, the increase in the dose was ruled out, and the patient completed 1 year of adjuvant therapy with no evidence of disease relapse.

摘要

我们报告了一位 44 岁女性患者,她主诉上腹痛,最初诊断为急性胰腺炎。3 个月后,症状再次出现,腹部计算机断层扫描显示十二指肠第三部分有一个肿块。手术后病理医生证实为恶性间叶组织增生,有丝分裂指数为 2 个/50HPF,无肿瘤坏死。增殖指数(Ki-67)为 2%。进行了突变分析,发现 c-KIT 外显子 9 中的突变,密码子 502 和 503 重复。患者拒绝根治性手术,考虑辅助治疗伊马替尼,初始剂量为 400mg/天,因为 c-KIT 外显子 9 的突变与伊马替尼反应不良相关,打算增加剂量至 800mg/天。然而,由于不良反应,排除了增加剂量,患者完成了 1 年的辅助治疗,没有疾病复发的证据。

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