Pancreatic acinar cell carcinoma-case report and literature review
- PMID: 30409114
- PMCID: PMC6225569
- DOI: 10.1186/s12885-018-5008-z
Pancreatic acinar cell carcinoma-case report and literature review
Abstract
Background: Pancreatic acinar cell carcinoma (ACC) is a rare tumor that constitutes 1% of all pancreatic neoplasms. Pancreatic ACC has unique characteristics in terms of biological behavior, imaging and prognosis.
Case presentation: The present study reported two cases of pancreatic ACC confirmed by postoperative pathology and both cases exhibited several different imaging features and laboratory test results. Both cases had approximately 4 cm mass located in uncinate process of pancreas. Dilated intra- and extra-hepatic bile ducts was observed in one case, along with calcification. Heterogeneous enhancement of the tumor was exhibited in both patients with different intensities. Obstructive jaundice, elevated α-fetoprotein and CA 19-9 was found in one case, while the other case had normal liver function and tumor markers.
Conclusions: It was difficult to accurately diagnose pancreatic ACC before the operation despite its unique characteristics. Radical resection was the best treatment modality for resectable pancreatic ACC.
Keywords: Acinar cell carcinoma; Diagnosis; Pancreas; Prognosis; Treatment.
Conflict of interest statement
Ethics approval and consent to participate
This study was reviewed and approved by the Ethics Committee of Beijing Chaoyang Hospital. Patients were not required to provide informed consent because the analysis used anonymous clinical data that were obtained after each patient agreed to treatment by written consent.
Consent for publication
Written informed consent was obtained from the patients for publication of these case reports and accompanying images.
Competing interests
The authors declare that they have no competing interests.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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