Primary pancreatic lymphoma-diagnosed on computed tomography: A rare case report
- PMID: 35401908
- PMCID: PMC8990050
- DOI: 10.1016/j.radcr.2022.02.058
Primary pancreatic lymphoma-diagnosed on computed tomography: A rare case report
Abstract
Primary pancreatic lymphoma is a rare disease. It comprises less than 0.5 % of pancreatic neoplasm and 0.1% of malignant lymphoma. It should be differentiated from pancreatic adenocarcinoma because management differs. At computed tomography, 2 types of morphology of primary pancreatic lymphoma have been described- a localized well-circumscribed tumoral form and another diffuse enlargement infiltrating or replacing most of the pancreatic gland. Here, we are presenting computed tomography (CT) imaging features of a case of primary pancreatic lymphoma in a 27 year old female who presented with a complaint of abdominal pain radiating to the back for 3 months and yellowish discoloration of sclera and skin for the last 15 days. In contrast-enhanced computed tomography an exophytic homogenously hypoenhancing mass arising from head and neck region of pancreas was seen. Involvement of common bile duct (CBD) and duodenum was there. The main pancreatic duct was not dilated. Common hepatic artery was encased by mass without arterial luminal narrowing or distortion. Diagnosis of primary pancreatic lymphoma was suggested on basis of imaging findings and further confirmed with fine-needle aspiration cytology.
Keywords: CT- Computed tomography, CBD- Commomn bile duct; Computed tomography; PET- Positron emission tomography, FNAC- Fine needle aspiration cytology; Pancreatic lymphoma; Primary pancreatic lymphoma; USG- Ultrasonography, HU- Hounsfield unit.
© 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington.
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