Pancreatic Neuroendocrine Carcinoma with Obstruction of Main Pancreatic Duct
10.2185/jjrm.63.659
- VernacularTitle:主膵管途絶をきたした膵神経内分泌癌の1例
- Author:
Kenji HIRAU
;
Masaji HASHIMOTO
;
Yutaka HIRANO
;
Kasumi TOZAWA
;
Kimito ORINO
;
Shinichi SASAKI
;
Masakatsu NAKAMURA
;
Kouhei HARIGANE
;
Jiajia LIU
;
Takuya YOSHIDA
- Publication Type:Journal Article
- From:Journal of the Japanese Association of Rural Medicine
2014;63(4):659-664
- CountryJapan
- Language:Japanese
-
Abstract:
Pancreatic neuroendocrine tumors, relatively rare cancers, mostly arise in the pancreatic parenchyma with infrequent involvement of the main pancreatic duct. Now and then, however, case reports have been published on pancreatic neuroendocrine carcinoma in which the main pancreatic duct is obstructed by tumor cells with severely fibrous stromal cells. Here, in this paper, we report a case of pancreatic neuroendocrine carcinoma with obstruction of the main pancreatic duct. A 59-year-old man complained of right upper abdominal pain. Magnetic resonance cholangiopancreatography and fat-suppressed T1-weighted magnetic resonance imaging showed gallbladder stones, a low-intensity-area measuring 8 mm in diameter in the pancreatic body, and club-shaped dilatation at the distal end of the pancreatic duct. The patient was thus diagnosed with a tumor in the pancreatic body and cholecystolithiasis, and underwent distal pancreatectomy and cholecystectomy. HE-staining showed tumor cells with eosinophilic cytoplasm and nuclear atypia. The infiltrative growth of the cells with severe fibrosis caused stenosis of the pancreatic duct. Based on the positive results of immunohistochemical staining for chromogranin A and synaptophysin and the Ki-67 index, the tumor was finally identified as pancreatic neuroendocrine carcinoma. The patient has been under follow-up with no additional treatment for >3 years since the surgery, without evidence of tumor recurrence.
