Wilde Brent K, Senger Jenna-Lynn, Kanthan Rani
Department of Pathology, Royal University and Saskatoon Health Region, Saskatchewan.
Can J Gastroenterol. 2010 Apr;24(4):233-6. doi: 10.1155/2010/943270.
Gastrointestinal schwannoma is a rare, benign pathological entity that can mimic colonic adenocarcinoma and cause diagnostic dilemmas for treatment. A case of a 68-year-old woman with colonic adenocarcinoma who was discovered to have an incidental synchronous bowel lesion that proved to be a gastrointestinal schwannoma and not a synchronous adenocarcinoma is described. Gastrointestinal schwannomas are uncommon in the colorectal region; they are most often located in the stomach. These spindle cell lesions are distinct from gastrointestinal stromal tumours because the tumour cells have a distinct immunophenotype, with strong diffuse positivity for S-100, glial fibrillary acidic protein and vimentin, and corroborative negative staining of CD34, CD117 and smooth muscle markers. Accurate diagnosis and recognition of this benign entity is, therefore, of immense clinicopathological value for accurate planning of therapeutic strategies.
胃肠道神经鞘瘤是一种罕见的良性病理实体,可酷似结肠腺癌并导致治疗中的诊断困境。本文描述了一例68岁患有结肠腺癌的女性病例,该患者被偶然发现同时存在肠道病变,经证实为胃肠道神经鞘瘤而非同步性腺癌。胃肠道神经鞘瘤在结直肠区域并不常见;它们最常位于胃部。这些梭形细胞病变与胃肠道间质瘤不同,因为肿瘤细胞具有独特的免疫表型,对S-100、胶质纤维酸性蛋白和波形蛋白呈强弥漫阳性,而CD34、CD117和平滑肌标志物呈阴性染色。因此,准确诊断和识别这种良性实体对于准确制定治疗策略具有巨大的临床病理价值。