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Acinar cell carcinoma with PRKAR1A and PTEN alterations and paraneoplastic panniculitis.

Authors :
Yang Z
Zarate Rodriguez JG
Beck H
Byrnes K
Trikalinos NA
Hammill CW
Source :
BMJ case reports [BMJ Case Rep] 2022 Dec 22; Vol. 15 (12). Date of Electronic Publication: 2022 Dec 22.
Publication Year :
2022

Abstract

Pancreatic acinar cell carcinoma is a rare type of pancreatic malignancy, which can be confused with pancreatic neuroendocrine neoplasm. Here, we describe a woman in her 80s who presented with abdominal pain and bilateral lower extremity panniculitis. She underwent surgery for a presumed diagnosis of neuroendocrine tumour with PTEN and PRKAR1A alterations; 19 months, later, a recurrence of her pancreatic malignancy was discovered. The patient underwent repeat resection and this time immunohistochemical staining confirmed the diagnosis of acinar cell carcinoma. Staining for acinar cell carcinoma should be prompted based on clinical suspicion in context of PTEN or PRKAR1A mutation when appropriate.<br />Competing Interests: Competing interests: None declared.<br /> (© BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ.)

Details

Language :
English
ISSN :
1757-790X
Volume :
15
Issue :
12
Database :
MEDLINE
Journal :
BMJ case reports
Publication Type :
Academic Journal
Accession number :
36549753
Full Text :
https://doi.org/10.1136/bcr-2022-251400