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胃神经束膜瘤。一种罕见的梭形细胞肿瘤,应与胃肠道间质瘤相鉴别。

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

作者信息

Agaimy Abbas, Wuensch Peter H

机构信息

Institute of Pathology, Clinic Centre Nuremberg, Prof.-Ernst-Nathan-Strasse 1, 90419 Nürnberg, Germany.

出版信息

Pathol Res Pract. 2005;201(6):463-7. doi: 10.1016/j.prp.2005.05.012.

DOI:10.1016/j.prp.2005.05.012
PMID:16136753
Abstract

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.

摘要

我们报告了首例良性神经束膜分化的周围神经鞘瘤(神经束膜瘤),该肿瘤表现为胃出血性肿块,患者为一名30岁的既往健康女性,就诊时无冯雷克林霍增氏病或其他原发性肿瘤的体征或迹象。胃切除标本显示为一个溃疡形成的中度细胞性间叶肿瘤,由细长的波浪状梭形细胞组成,呈束状和片状排列,有局灶性漩涡形成,偶尔可见深色染色的细胞区域和浅色染色的低细胞区域交替。肿瘤细胞对上皮膜抗原、CD56(N-CAM)和波形蛋白呈强免疫反应,但对S-100蛋白及其他谱系特异性上皮、间叶、血液淋巴和网状组织细胞标记物呈阴性。CD117显示有大量阳性染色的肥大细胞,但病变细胞无反应。我们推测,这种不寻常的胃肿瘤的组织学和免疫组化综合特征与神经束膜瘤诊断相符,其生物学行为可能为良性。据我们所知,这是胃神经束膜瘤的首例报告,胃神经束膜瘤是一种极其罕见的间叶病变,在胃肠道间质瘤的鉴别诊断中应予以考虑,尤其是所谓的KIT阴性胃肠道间质瘤。胃肠道神经束膜瘤可能未得到充分认识,因为我们的病例最初被诊断为良性胃肠道间质瘤。

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