RT Journal Article
SR Electronic
T1 Primary pancreatic lymphoma
JF Saudi Medical Journal
JO Saudi Med J
FD Prince Sultan Military Medical City
SP 307
OP 312
DO 10.15537/smj.2024.45.3.20230930
VO 45
IS 3
A1 Al-Maghrabi, Jaudah A.
YR 2024
UL http://smj.org.sa/content/45/3/307.abstract
AB Objectives: To report the histopathological pattern of primary pancreatic lymphoma (PPL) in 2 tertiary hospitals.Methods: The pathology slides and reports of all the cases diagnosed in pathology departments in 2 referral hospitals were reviewed. An additional immunohistochemistry study was done to reclassify lymphomas according to the current system.Results: Eight patients with PPL have been identified. The ages ranged from 36 to 71 years. Clinical presentation includes abdominal pain, weight loss, jaundice, abdominal mass, nausea, and vomiting. Pathological evaluation revealed 5 diffuse large B-cell lymphomas, one high-grade B-cell lymphoma, one MALT lymphoma, and one follicular lymphoma.Conclusion: Primary pancreatic lymphoma is a very rare tumor without specific clinical, laboratory tests, or radiological findings. Abdominal pain is the most common clinical presentation. Diffuse large b-cell lymphoma is the most common pathological subtype. Primary pancreatic lymphoma should be taken into consideration when evaluating pancreatic mass to avoid unnecessary surgical resection.