Sawahashi Satoko, Abe Yasuaki, Suzuki Fumiya, Nabeshima Tatsuhide, Shoji Masakuni, Nakamura Takuya, Nishise Yuko, Kuroki Michio, Otake Hiroya, Hirakawa Hidetoshi
Department of Gastroenterology, Yamagata City Hospital Saiseikan.
Department of Pathology, Yamagata City Hospital Saiseikan.
Nihon Shokakibyo Gakkai Zasshi. 2022;119(5):452-458. doi: 10.11405/nisshoshi.119.452.
Intraductal papillary mucinous carcinoma (IPMC) arising from the heterotopic pancreas is rare. A case of IPMC metastasis from the jejunal heterotopic pancreas was described. The heterotopic pancreas could be the source of the submucosal tumor-like lesion found in the small intestine with an elevated carbohydrate antigen (CA) 19-9 level. A 60-year-old woman was admitted to the hospital with pulmonary thromboembolism and anemia. The level of CA19-9, a tumor marker, was found to be 211.8U/ml. A tumor in the jejunum was discovered using contrast-enhanced computed tomography. There were also a number of hepatic tumors found. A submucosal tumor-like lesion in the jejunum was discovered during an enteroscopy, and a biopsy revealed it to be an adenocarcinoma. Partial resection of the jejunum was performed to control hemorrhage. Histopathology revealed an invasive IPMC arising from a heterotopic pancreas (Heinrich type II) and chemotherapy with gemcitabine and nab-paclitaxel was initiated. There have only been three cases of invasive IPMC from a heterotopic pancreas reported, and this is the first one to include chemotherapeutic treatment of distant metastasis.
起源于异位胰腺的导管内乳头状黏液性癌(IPMC)较为罕见。本文描述了一例来自空肠异位胰腺的IPMC转移病例。异位胰腺可能是在小肠中发现的黏膜下肿瘤样病变的来源,其碳水化合物抗原(CA)19-9水平升高。一名60岁女性因肺血栓栓塞和贫血入院。肿瘤标志物CA19-9水平为211.8U/ml。通过增强计算机断层扫描在空肠发现一个肿瘤。还发现了一些肝脏肿瘤。在肠镜检查中发现空肠有一个黏膜下肿瘤样病变,活检显示为腺癌。为控制出血进行了空肠部分切除术。组织病理学显示为起源于异位胰腺的浸润性IPMC(海因里希II型),并开始使用吉西他滨和纳米白蛋白结合型紫杉醇进行化疗。此前仅报道过3例来自异位胰腺的浸润性IPMC病例,这是首例包括对远处转移进行化疗的病例。