Loughrey M B, Mitchell C, Mann G B, Michael M, Waring P M
Department of Pathology, Peter MacCallum Cancer Centre, Melbourne, VIC 3002, Australia.
J Clin Pathol. 2005 Jul;58(7):779-81. doi: 10.1136/jcp.2004.023226.
This report describes a case of unresectable primary gastrointestinal stromal tumour (GIST) treated with imatinib on a neoadjuvant basis, before subsequent successful surgical resection. After six months of imatinib, computed tomography and positron emission tomography imaging demonstrated a significant size reduction and complete metabolic response to treatment, rendering the tumour resectable. Mutational analysis showed an activating KIT mutation in exon 11. The pathological appearance of the resected tumour was heterogeneous with extensive necrosis, cystic and myxoid change, extensive hypocellularity, and patchy foci of residual viable tumour. The implications for this management option of radiological, pathological, and molecular assessment are discussed.
本报告描述了一例不可切除的原发性胃肠道间质瘤(GIST),在随后成功进行手术切除之前,先接受了伊马替尼新辅助治疗。接受伊马替尼治疗六个月后,计算机断层扫描和正电子发射断层扫描成像显示肿瘤大小显著缩小,对治疗有完全代谢反应,使肿瘤可切除。突变分析显示第11外显子存在激活的KIT突变。切除肿瘤的病理表现具有异质性,伴有广泛坏死、囊性和黏液样改变、广泛细胞减少以及残留存活肿瘤的散在灶。讨论了这种管理方案在放射学、病理学和分子评估方面的意义。