Frejlich Ewelina, Rudno-Rudzińska Julia, Hałoń Agnieszka, Kielan Wojciech, Grzebianiak Zygmunt
Klinika Chirurgii Ogólnej i Chirurgii Onkologicznej, Uniwersytecki Szpital Kliniczny we Wrocławiu.
Zakład Patomorfologii i Cytologii Onkologicznej, Uniwersystet Medyczny we Wrocławiu.
Wiad Lek. 2013;66(3):249-52.
Schwannoma is a rare, usually benign, generally slow growing, asymptomatic mesenchymal neoplasm derived from nerve cells. In the gastrointestinal tract the most common localization is stomach and the gastric schwannomas represent about 0.2% of all gastric neoplasms. We present a case of 44-years-old male admitted to 2nd Department of General Surgery and Oncological Surgery Medical University for treatment of a submucosal gastric tumor detected in upper gastrointestinal endoscopy, endoscopic ultrasonography and computed tomography (CT). Patient presented with no gastrointestinal disorders and the random endoscopy revealed a gastric tumor, but the biopsy of the lesion showed no carcinomas' cells and the suspicion of GIST. CT confirms the presence of the 5 cm large gastric tumor and intraabdominal lymphadenopathy. The patient was directed to surgery because of the malignant risk. The subtotal gastrectomy with BII anastomosis was performed and no perioperative complications were observed. The postoperative histopathological examination revealed a typical morphology and immunophenotype of tumor. The neoplastic cells were immunoreactive with S-100 protein, but lacked immunoreactivity with CD 117, CD 34 and smooth-muscle actin (SMA). The histopathologic features and immunohistochemical staining pattern were consistent with a gastric schwannoma. The lymph nodes resected, during the operation revealed reactive inflammatory changes without evidence of neoplastic cells and any malignancy. 10-month after the surgery patient has no complains but the follow up will be continued. This case underscores the importance of including gastric schwannomas in the differential diagnosis when preoperative imaging studies reveal a submucosal, exophytic gastric mass.
施万细胞瘤是一种罕见的、通常为良性、生长一般缓慢且无症状的间叶性肿瘤,起源于神经细胞。在胃肠道中,最常见的部位是胃,胃施万细胞瘤约占所有胃肿瘤的0.2%。我们报告一例44岁男性患者,因上消化道内镜检查、内镜超声检查和计算机断层扫描(CT)发现胃黏膜下肿瘤,入住医科大学普通外科和肿瘤外科第二科室接受治疗。患者无胃肠道疾病症状,随机内镜检查发现胃肿瘤,但病变活检未发现癌细胞,怀疑为胃肠道间质瘤(GIST)。CT证实存在一个5厘米大的胃肿瘤及腹腔内淋巴结肿大。由于存在恶性风险,患者接受了手术。实施了胃次全切除术及毕Ⅱ式吻合术,未观察到围手术期并发症。术后组织病理学检查显示肿瘤具有典型的形态和免疫表型。肿瘤细胞对S-100蛋白呈免疫反应,但对CD 117、CD 34和平滑肌肌动蛋白(SMA)缺乏免疫反应。组织病理学特征和免疫组化染色模式与胃施万细胞瘤一致。手术中切除的淋巴结显示为反应性炎症改变,未发现肿瘤细胞及任何恶性迹象。术后10个月患者无不适,但仍将继续随访。该病例强调了术前影像学检查显示胃黏膜下外生性肿块时,将胃施万细胞瘤纳入鉴别诊断的重要性。