Pancreatic Mixed Acinar-neuroendocrine-ductal Carcinoma: A Case Report and Literature Review

Pancreatic mixed neoplasms are very rare. We herein report a unique case of pancreatic mixed acinar-neuroendocrine-ductal carcinoma with trilineage differentiation. The patient was an 83-year-old woman referred to our hospital due to anemia and a pancreatic mass. Contrast-enhanced computed tomograph...

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Published inInternal Medicine Vol. 62; no. 22; pp. 3347 - 3353
Main Authors Sakaguchi, Ryohei, Yamada, Reiko, Nose, Kenji, Tanaka, Takamitsu, Murashima, Yumi, Tsuboi, Junya, Nakagawa, Hayato
Format Journal Article
LanguageEnglish
Published Japan The Japanese Society of Internal Medicine 15.11.2023
Japan Science and Technology Agency
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Summary:Pancreatic mixed neoplasms are very rare. We herein report a unique case of pancreatic mixed acinar-neuroendocrine-ductal carcinoma with trilineage differentiation. The patient was an 83-year-old woman referred to our hospital due to anemia and a pancreatic mass. Contrast-enhanced computed tomography revealed a 60-mm mass in the pancreas. Subtotal stomach-preserving pancreaticoduodenectomy was performed. The postoperative pathological diagnosis was mixed acinar-neuroendocrine-ductal carcinoma. Postoperative chemotherapy was conducted according to the adenocarcinoma and neuroendocrine carcinoma protocols. The patient died 26 months postoperatively. Choosing appropriate chemotherapy for mixed neoplasms is difficult. Cancer gene panel testing, if possible, may support the choice of therapeutic agents.
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Review-3
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ObjectType-Feature-5
ObjectType-Article-4
ObjectType-Report-1
Correspondence to Dr. Reiko Yamada, reiko-t@med.mie-u.ac.jp
ISSN:0918-2918
1349-7235
DOI:10.2169/internalmedicine.1298-22