Masulović Dragan, Stevic Ruza, Filipović A, Micev Marjan, Ivanović Aleksandar
Acta Chir Iugosl. 2013;60(3):61-4. doi: 10.2298/aci1303061m.
Somatostatinomas are rare functioning neoplasms usually arising in the pancreas and duodenum. They are seldom associated with typical clinical symptoms. Their diagnosis is confirmed only by histological and immunohistochemical studies and the presence of specific hormones. Two distinct clinicopathological forms of somatostatinoma exist: duodenal and pancreatic somatostatinomas. Clinically, compared to pancreatic somatostatinomas, duodenal somatostatinomas are more often associated with nonspecific symptoms and neurofibromatosis, but less often with somatostatinoma syndrome or metastasis. We report a case of somatostatin-producing duodenal carcinoma in a 45-year-old female with neither neurofibromatosis nor somatostatinoma syndrome. Abdominal computed tomography showed a 18 mm mass in the duodenum which had given rise to multiple lymph node metastases. Although the endoscopic biopsies were free of malignancy, the patient subsequently underwent Whipple's operation for the duodenal mass. Immunohistochemical analysis confirmed the diagnosis of somatostatin-producing carcinoma.
生长抑素瘤是一种罕见的功能性肿瘤,通常起源于胰腺和十二指肠。它们很少伴有典型的临床症状。其诊断仅通过组织学和免疫组织化学研究以及特定激素的存在来证实。生长抑素瘤存在两种不同的临床病理形式:十二指肠生长抑素瘤和胰腺生长抑素瘤。临床上,与胰腺生长抑素瘤相比,十二指肠生长抑素瘤更常伴有非特异性症状和神经纤维瘤病,但较少伴有生长抑素瘤综合征或转移。我们报告一例45岁女性的分泌生长抑素的十二指肠癌病例,该患者既没有神经纤维瘤病也没有生长抑素瘤综合征。腹部计算机断层扫描显示十二指肠有一个18毫米的肿块,并已引起多处淋巴结转移。尽管内镜活检未发现恶性肿瘤,但患者随后因十二指肠肿块接受了惠普尔手术。免疫组织化学分析证实了分泌生长抑素癌的诊断。