Kuhlgatz Jens, Sander Bjoern, Golas Mariola Monika, Gunawan Bastian, Schulze Thorsten, Schulten Hans-Jürgen, Wardelmann Eva, Füzesi László
Department of General and Visceral Surgery, Albert Schweitzer Hospital, Northeim, Germany.
Int J Colorectal Dis. 2006 Jan;21(1):84-8. doi: 10.1007/s00384-004-0730-1. Epub 2005 May 5.
Strategies for the diagnosis of tumors arising in the intestinal muscular wall are rapidly evolving. Immunoreactivity for CD117 (KIT) usually supports the diagnosis of gastrointestinal stromal tumor (GIST), but a small subset of GISTs lacks KIT expression. In these cases the differential diagnosis of KIT-negative GIST versus one of their morphological mimics is difficult and bears critical implications for therapeutic management.
Here, we report a case of a KIT-negative smooth muscle cell tumor of the colon in a 21-year-old man with the clinical appearance of GIST. Mutations of the KIT and platelet-derived growth factor receptor alpha (PDGFRA) gene could be ruled out. No chromosomal imbalances characteristic of GIST were found. However, cytogenetic analysis revealed losses at 7q, which has previously been reported in cases of uterine leiomyoma.
We discuss current approaches to the differential diagnosis of true gastrointestinal smooth muscle cell tumor versus GIST.
肠道肌壁肿瘤的诊断策略正在迅速发展。CD117(KIT)免疫反应性通常支持胃肠道间质瘤(GIST)的诊断,但一小部分GIST缺乏KIT表达。在这些情况下,KIT阴性GIST与其形态学模仿物之一的鉴别诊断很困难,且对治疗管理具有关键意义。
在此,我们报告一例21岁男性的结肠KIT阴性平滑肌细胞瘤,临床表现为GIST。KIT和血小板衍生生长因子受体α(PDGFRA)基因的突变可以排除。未发现GIST特有的染色体失衡。然而,细胞遗传学分析显示7号染色体长臂缺失,这在子宫平滑肌瘤病例中曾有报道。
我们讨论了目前鉴别真性胃肠道平滑肌细胞瘤与GIST的方法。