Ma Jinfeng, Kimura Wataru, Takeshita Akiko, Hirai Ichiro, Moriya Toshiyuki, Mizutani Masaomi
Department of Gastroenterology and General Surgery Graduate School of Medicine, University of Yamagata, Yamagata, Japan.
Hepatogastroenterology. 2007 Oct-Nov;54(79):1945-50.
Neuroendocrine carcinoma of the stomach is an uncommon tumor, usually associated with highly malignant biological behavior and extremely poor prognosis. In this report, we described a case of advanced neuroendocrine carcinoma of the stomach with the peripancreatic lymph node metastases which was treated with pancreaticoduodenectomy with extended lymphadenectomy. The patient was admitted to our hospital for anemia. An upper gastrointestinal endoscopy revealed a 4x4-cm fungating tumor with its fundus locating mainly in the duodenal bulbus and extending to the gastric antrum, and tumor biopsy revealed the histological findings of adenocarcinoma. Computed tomography (CT) showed a large mass in the duodenal bulbus with regional lymph node metastases. The patient's disease was diagnosed as primary duodenal cancer with regional lymph node metastases preoperatively. During the operation, an obviously swollen lymph node on the anterior surface of the head of the pancreas 4.0 x 3.5 cm in size was found growing into the parenchyma of the pancreas head and could not be separated from the pancreas, and the swollen lymph node along the superior mesenteric vein was also hard and suspected to be a metastatic node. A pancreaticoduodenectomy with extended lymphadenectomy was performed to achieve a radical resection. Histopathologically, the origin of the primary tumor was considered as a gastric origin, and the tumor was composed of diffused small cells with a moderate mitotic index and occasional rosette formation. Immunohistochemical investigations of the neoplastic cells confirmed the tumor to be neuroendocrine carcinoma. The obvious swollen lymph node on the anterior surface of the head of the pancreas and the swollen lymph node along the superior mesenteric vein were also identified as metastatic lymph nodes. Adjuvant chemotherapy with TS-1 was administered on an out-patient basis 6 weeks after the operation. The patient is well and has now been free of symptoms of recurrence and metastasis for 8 months.
胃神经内分泌癌是一种罕见的肿瘤,通常具有高度恶性的生物学行为且预后极差。在本报告中,我们描述了一例晚期胃神经内分泌癌伴胰周淋巴结转移的病例,该患者接受了胰十二指肠切除术及扩大淋巴结清扫术。患者因贫血入院。上消化道内镜检查发现一个4×4厘米的蕈状肿瘤,其底部主要位于十二指肠球部并延伸至胃窦,肿瘤活检显示为腺癌的组织学表现。计算机断层扫描(CT)显示十二指肠球部有一个大肿块并伴有区域淋巴结转移。患者的疾病术前被诊断为原发性十二指肠癌伴区域淋巴结转移。手术过程中,发现胰腺头部前表面有一个明显肿大的淋巴结,大小为4.0×3.5厘米,已长入胰头实质且无法与胰腺分离,沿肠系膜上静脉的肿大淋巴结也质地坚硬,怀疑为转移淋巴结。遂行胰十二指肠切除术及扩大淋巴结清扫术以实现根治性切除。组织病理学检查认为原发性肿瘤起源于胃,肿瘤由弥漫性小细胞组成,有中度的有丝分裂指数且偶尔形成菊形团。对肿瘤细胞进行免疫组织化学检查证实该肿瘤为神经内分泌癌。胰腺头部前表面明显肿大的淋巴结及沿肠系膜上静脉的肿大淋巴结也被确定为转移淋巴结。术后6周在门诊给予替吉奥辅助化疗。患者情况良好,目前已无复发和转移症状8个月。