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Perineurioma of the stomach. A rare spindle cell neoplasm that should be distinguished from gastrointestinal stromal tumor.

机译:胃神经鞘瘤。稀有的梭形细胞瘤,应与胃肠道间质瘤区分开。

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We report on the first case of benign perineurially differentiated peripheral nerve sheath tumor (perineurioma) presenting as a bleeding gastric mass in a 30-year-old, previously healthy woman with no signs or stigmata of von Recklinghausen's disease or other primary tumor at time of presentation. Gastric resection specimen revealed an ulcerated moderately cellular mesenchymal tumor consisting of elongated wavy spindle cells arranged in a fascicular and sheet-like pattern with focal whorling and occasional alternation of dark staining cellular and light staining hypocellular areas. Tumor cells were strongly immunoreactive for epithelial membrane antigen, CD56 (N-CAM), and vimentin, but were negative for S-100-protein and other lineage-specific epithelial, mesenchymal, hematolymphoid, and reticulo-histiocytic markers. CD117 revealed numerous positive staining mast cells, but the lesional cells were not reacting. We presume that the combined histological and immunohistochemical profiles of this unusual gastric neoplasm are consistent with a diagnosis of perineurioma with a probably benign biological behavior. To our knowledge, this is the first report of gastric perineurioma, an extremely rare mesenchymal lesion that should be considered among the differential diagnoses of gastrointestinal stromal tumor, especially the so-called KIT-negative GIST. Gastrointestinal perineuriomas might be under-recognized, as our case was initially diagnosed as a benign GIST.
机译:我们报道了30例先前健康的女性中出现出血性胃肿块的第一例良性会阴部分化型周围神经鞘瘤(perineurioma),当时尚无von Recklinghausen病或其他原发肿瘤的体征或柱头。介绍。胃切除标本显示为溃疡性中度细胞间质瘤,由呈波浪状纺锤形细胞排列成束状和片状图案,伴有局灶性ling毛,偶尔有暗染的细胞和浅染的低细胞区域交替出现。肿瘤细胞对上皮膜抗原,CD56(N-CAM)和波形蛋白具有强烈的免疫反应性,但对S-100蛋白和其他谱系特异性上皮,间充质,血淋巴和网状组织细胞标记物呈阴性。 CD117显示出许多阳性染色的肥大细胞,但病变细胞没有反应。我们认为,这种不寻常的胃肿瘤的组织学和免疫组化特征相结合,可以诊断出具有可能是良性生物学行为的神经鞘瘤。据我们所知,这是胃神经尿瘤瘤的首次报道,胃神经瘤瘤是一种极为罕见的间质病变,应在胃肠道间质瘤的鉴别诊断中考虑,尤其是所谓的KIT阴性GIST。由于我们的病例最初被诊断为良性GIST,因此胃肠道神经鞘瘤可能未被充分认识。

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