Pancreatic hepatoid carcinoma: A rare form of pancreatic neoplasm

16Citations
Citations of this article
17Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Primary pancreatic hepatoid carcinoma (PHC) is extremely rare, resembling hepatocellular carcinoma (HCC) in terms of morphology and immunohistochemical features. Hepatoid carcinoma can present in other organs, most noticeably in the stomach. PHC is present in two forms either a pure form like HCC or admixed with other histologic tumor components characteristic of the underlying primary site (endocrine tumors, ductal, or acinar adenocarcinomas). Here, we report a 69-year-old male patient with distal pancreatic mass incidentally found during a CT scan workup for a pulmonary nodule suspicious for metastatic prostate adenocarcinoma. We described the clinical, cytological, and histological finding and conducted a literature review.

Cite

CITATION STYLE

APA

Soofi, Y., Kanehira, K., Abbas, A., Aranez, J., Bain, A., & Ylagan, L. (2015). Pancreatic hepatoid carcinoma: A rare form of pancreatic neoplasm. Diagnostic Cytopathology, 43(3), 251–256. https://doi.org/10.1002/dc.23195

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free