Pancreatic lymphoma: Case report

2021 ◽  
Vol 157 (6) ◽  
pp. 298-299
Author(s):  
Cristina Rubín de Célix ◽  
Celia Gómez-Labrador ◽  
Jorge Mendoza
2018 ◽  
Vol 2018 ◽  
pp. 1-4 ◽  
Author(s):  
Venkata Rajesh Konjeti ◽  
Gerald M. Hefferman ◽  
Sravanthi Paluri ◽  
Prerna Ganjoo

Primary pancreatic lymphoma (PPL) is of very rare occurrence as an extra nodal site of Non-Hodgkin’s lymphoma (NHL). It represents less than 1% of NHL. Out of which Burkitt lymphoma of pancreas is of a rare presentation. It usually occurs in children and presenting in adults is uncommon. The prevalence of pancreatic Burkitt lymphoma is not known as the incidence is significantly low. Clinical features of PPL are predominantly nonspecific and can become difficult with associated inflammation of pancreas. Differentiation of lymphoma to adenocarcinoma is important as chemotherapy is the main stay of treatment in lymphoma. We report a case of 68-year-old female who presented with nonspecific symptoms and was found to have obstructive jaundice secondary to pancreatic head neoplasm which was proved to be pancreatic Burkitt lymphoma which is a rare presentation.


2003 ◽  
Vol 30 (2) ◽  
pp. 121-125
Author(s):  
Naoyasu Yoshida ◽  
Masaru Nakamura ◽  
Hiroyasu Yamada

2010 ◽  
Vol 63 (2) ◽  
pp. 167
Author(s):  
Tae Wook Heo ◽  
Jin Woong Kim ◽  
Suk Hee Heo ◽  
Sang Soo Shin ◽  
Yong Yeon Jeong ◽  
...  

Author(s):  
Cristina Rubín de Célix ◽  
Celia Gómez-Labrador ◽  
Jorge Mendoza

2000 ◽  
Vol 17 (3) ◽  
pp. 237-247 ◽  
Author(s):  
JR Salvatore ◽  
B Cooper ◽  
I Shah ◽  
T Kummet

2021 ◽  
Vol 7 (1) ◽  
pp. 20-22
Author(s):  
Robert A. Ries ◽  
Christina L. Jacovides ◽  
Jennifer Rashti ◽  
Jerald Z. Gong ◽  
Charles J. Yeo

2018 ◽  
Vol 5 ◽  
pp. 141-146
Author(s):  
Bradley Aaron Cagle ◽  
Brenda L. Holbert ◽  
Stephanie Wolanin ◽  
Rafel Tappouni ◽  
Neeraj Lalwani

2020 ◽  
pp. 49-51
Author(s):  
Vikram Chaturvedi ◽  
Rituparna Chaturvedi ◽  
Sharmistha Debnath ◽  
Abhishek Mishra

Primary pancreatic lymphoma (PPL) is an extremely rare disease, with few cases reported in literature. Clinical manifestations are usually nonspecific and mimic other pancreatic diseases. Owing to paucity of data and experience of PPL, clinico-pathological features, differential diagnosis, optimal treatment and overall outcomes are not well known. Varicella zoster virus (VZV) is known to cause varicella in children and herpes zoster in adults. Acute pancreatitis caused by VZV is a rare and serious complication, with immunocompromised individuals being primarily affected. We report a case of VZV associated acute pancreatitis in a patient who was diagnosed and treated for primary pancreatic lymphoma, thus rendering her immunocompromised and susceptible to developing infectious pancreatitis. A 56 year old female patient presented with recurrent vomiting, upper abdominal pain and hyperaesthesia in the right upper quadrant of 2 days duration. Following admission her right sided abdominal pain worsened (stabbing pain) and a diagnosis of acute pancreatitis was confirmed based on elevated serum amylase levels and CT scan findings of pancreatic enlargement. The patient was managed conservatively with intravenous fluids, antibiotics, analgesics and topical acyclovir ointment. The patient continues to be asymptomatic after 5 years of follow up. Though extremely rare, a diagnosis of herpes zoster pancreatitis should be considered in such patients, and prompt treatment initiated to prevent further deterioration and to minimize mortality. Core tip: Primary pancreatic lymphoma is in itself a very rare disease, and our patient having presented with herpes zoster associated acute pancreatitis in a background of PPL makes this case even rarer. This is probably the first case report of herpes zoster associated acute pancreatitis in an immunocompromised patient due to primary pancreatic lymphoma.


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