He Cheng-Hai, Lin Shi-Hua, Chen Zhen, Li Wei-Min, Weng Chun-Yan, Guo Yun, Li Guo-Dong
Department of Gastroenterology, The Affiliated Hospital of Hangzhou Normal University, Hangzhou 310000, Zhejiang Province, China.
Department of Internal Medicine, Zhejiang Hospital, Hangzhou 310000, Zhejiang Province, China.
World J Gastrointest Surg. 2022 Apr 27;14(4):362-369. doi: 10.4240/wjgs.v14.i4.362.
Schwannomas, also known as neurinomas, are benign tumors derived from Schwann cells. Gastrointestinal schwannomas are rare and are most frequently reported in the stomach. They are usually asymptomatic and are difficult to diagnose preoperatively; however, endoscopy and imaging modalities can provide beneficial preliminary diagnostic data. There are various surgical options for management. Here, we present a case of a large gastric schwannoma (GS) managed by combined laparoscopic and endoscopic surgery.
A 28-year-old woman presented with a 2-mo history of epigastric discomfort and a feeling of abdominal fullness. On upper gastrointestinal endoscopy and endoscopic ultrasonography, a hypoechogenic submucosal mass was detected in the gastric antrum: It emerged from the muscularis propria and projected intraluminally. Computed tomography showed a nodular lesion (4 cm × 3.5 cm), which exhibited uniform enhancement, on the gastric antrum wall. Based on these findings, a preliminary diagnosis of gastrointestinal stromal tumor was established, with schwannoma as a differential. Considering the large tumor size, we planned to perform endoscopic resection and to convert to laparoscopic treatment, if necessary. Eventually, the patient underwent combined laparoscopic and gastroscopic surgery. Immunohistochemically, the resected specimen showed positivity for S-100 and negativity for desmin, DOG-1, α-smooth muscle actin, CD34, CD117, and p53. The Ki-67 index was 3%, and a final diagnosis of GS was established.
Combined laparoscopic and endoscopic surgery is a minimally invasive and effective treatment option for large GSs.
施万细胞瘤,也称为神经鞘瘤,是源自施万细胞的良性肿瘤。胃肠道施万细胞瘤罕见,最常报道于胃部。它们通常无症状,术前难以诊断;然而,内镜检查和影像学检查可提供有益的初步诊断数据。治疗有多种手术选择。在此,我们报告一例通过腹腔镜和内镜联合手术治疗的巨大胃施万细胞瘤(GS)病例。
一名28岁女性,有2个月上腹部不适和腹胀感病史。上消化道内镜检查和内镜超声检查发现胃窦部有一个低回声黏膜下肿块:它起源于固有肌层并向腔内突出。计算机断层扫描显示胃窦壁有一个结节性病变(4 cm×3.5 cm),呈均匀强化。基于这些发现,初步诊断为胃肠道间质瘤,鉴别诊断为施万细胞瘤。考虑到肿瘤体积较大,我们计划进行内镜切除,必要时转为腹腔镜治疗。最终,患者接受了腹腔镜和胃镜联合手术。免疫组织化学检查显示,切除标本S - 100阳性,结蛋白、DOG - 1、α - 平滑肌肌动蛋白、CD34、CD117和p53阴性。Ki - 67指数为3%,最终确诊为GS。
腹腔镜和内镜联合手术是治疗巨大GS的一种微创且有效的治疗选择。