伊马替尼治疗后免疫表型改变的胃肠道间质瘤的诊断考虑:1例报告和文献复习

Jihuan Chen , Liz M. Yang , Jonathan Somma , Yujun Gan , Zengying Wu , Zhiyan Fu
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引用次数: 0

摘要

胃肠道间质瘤(gist)是胃肠道最常见的间质肿瘤,具有较高的复发和转移率。使用包括KIT/CD117和DOG1在内的免疫组织化学(IHC)面板可以在98%以上的病例中进行准确诊断。然而,在酪氨酸激酶抑制剂治疗后,一些病例可能表现出组织学上的去分化和KIT/CD117和DOG1表达的缺失,这可能导致难以确认复发或持续性疾病。我们报告了这样一个病例,伊马替尼治疗,CD117和DOG1双阴性,转移到肝脏的GIST在一个55岁的女性,需要分子分析来确认诊断。认识和认识这一现象对胃肠道间质瘤患者的准确诊断和治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic considerations for gastrointestinal stromal tumors with altered immunophenotype following Imatinib treatment: A case report and literature review
Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors in the gastrointestinal tract and have a high rate of recurrence and metastasis. Using an immunohistochemical (IHC) panel including KIT/CD117 and DOG1 allows for accurate diagnosis in more than 98% of cases. However, after tyrosine kinase inhibitor treatment, some cases can exhibit histologic dedifferentiation and loss of KIT/CD117 and DOG1 expression that may cause difficulty in confirming recurrent or persistent disease. We present such a case of an Imatinib treated, CD117 and DOG1 dual negative, metastatic GIST to the liver in a 55-year-old female which required molecular analysis to confirm the diagnosis. Awareness and recognition of this phenomenon is crucial for the accurate diagnosis and management of patients with GISTs.
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