Guan Bing, Li Xiao-Hong, Wang Liang, Zhou Min, Dong Zhi-Wu, Luo Guo-Jun, Meng Ling-Ping, Hu Jun, Jin Wei-Yun
Department of Pathology Department of Sterile and Supply Center Department of Gastroenterology Department of Respirology Department of Laboratory Department of Neurology Department of Radiology Department of Hepatobiliary Surgery Department of Hematologic Oncology, Shanghai 6th People's Hospital Jinshan Branch, Shanghai, PR China.
Medicine (Baltimore). 2018 Jul;97(27):e11461. doi: 10.1097/MD.0000000000011461.
Splenosis is the heterotopic auto-transplantation of the splenic tissues. Gastric splenosis in a rare location mimics a gastrointestinal stromal tumor (GIST). Gastric splenosis with hemangioma has not been reported throughout the literature.
We report a case of a 74-year-old schistosomiasis cirrhosis splenectomy woman diagnosed with gastric fundus mass. Preoperative computed tomography and endoscopic ultrasonography revealed findings suggestive of a GIST.
The mass located in the gastric fundus muscularis propria, measuring 3.9 × 2.8 × 2.4 cm with a dark red color, was removed by surgery. In the mass, a 1 × 1-cm red-purple nodule was also found. On microscopic examination, a well-formed splenic tissue divided into two compartments-white pulp and red pulp-separated by an ill-defined interphase known as the marginal zone. However, a nodule in the heterotopic spleen was mainly composed of larger thin-walled muscular vessels. The final diagnosis was gastric splenosis with hemangioma.
After discussion in a multidisciplinary conference, the patient was considered for a GIST resection under gastroscopy. In the process of peeling, the surface of the mucosal, submucosal, muscle layers and the tumor surface were diffusely oozing. The effect of electrocoagulation and hemostasis was extremely poor. Therefore, endoscopic surgery was arrested. After dealing with the patient's family, a combination of laparoscopic-gastroscope double-mirror surgery was decided in accordance with the principle of minimally invasive surgery to preserve the stomach. Owing to several adhesions and concealed the location of tumor, we stopped the double-mirror combination surgery plan. Considering the great possibility of a malignant GIST, we still decided to continue the traditional surgical resection. The tumor was then removed via surgery OUTCOMES:: The patient was favorable with healing and discharged on postoperative day 10.
Gastric splenosis with an associated hemangioma is the first well-documented case. Its pathogenesis may be direct implantation. Appropriate medical history taking and Tc-99 m heat-denatured RBC spleen scintigraphy (Tc-99MHDRS) are valuable for its diagnosis; however, pathology is the gold standard. Surgery is a reasonable treatment for gastric splenosis with hemangioma.
脾组织异位自体移植即脾组织植入。罕见部位的胃脾组织植入可酷似胃肠道间质瘤(GIST)。胃脾组织植入合并血管瘤在文献中未见报道。
我们报告一例74岁血吸虫性肝硬化脾切除术后女性,诊断为胃底肿物。术前计算机断层扫描和内镜超声检查结果提示为GIST。
位于胃底固有肌层的肿物,大小为3.9×2.8×2.4 cm,呈暗红色,手术切除。肿物内还发现一个1×1 cm的红紫色结节。显微镜检查显示,形成良好的脾组织分为白髓和红髓两个区域,由边界不清的边缘区分隔。然而,异位脾脏中的结节主要由较大的薄壁肌性血管组成。最终诊断为胃脾组织植入合并血管瘤。
多学科会诊讨论后,考虑对患者进行胃镜下GIST切除术。剥离过程中,黏膜、黏膜下层、肌层表面及肿瘤表面弥漫性渗血。电凝止血效果极差。因此,停止内镜手术。与患者家属沟通后,根据微创手术原则决定采用腹腔镜-胃镜双镜联合手术以保留胃。由于存在多处粘连且肿瘤位置隐匿,我们放弃了双镜联合手术方案。考虑到GIST恶性可能性大,我们仍决定继续进行传统手术切除。随后通过手术切除肿瘤。
患者恢复良好,术后第10天出院。
胃脾组织植入合并血管瘤是首例有充分文献记载的病例。其发病机制可能为直接植入。详细的病史采集和99m锝热变性红细胞脾脏闪烁显像(Tc-99mHDRS)对其诊断有重要价值;然而,病理检查是金标准。手术是治疗胃脾组织植入合并血管瘤的合理方法。