Autopsy and Case Reports (Sep 2012)

Burkitt lymphoma mimicking acute pancreatitis

  • Lívia Moscardi Bacchi,
  • Ivan Ucella,
  • Thiago Trolez Amancio,
  • Marianne Castro Gonçalves,
  • Renata Bacic Palhares,
  • Sheila Aparecida Coelho Siqueira

DOI
https://doi.org/10.4322/acr.%y.48194
Journal volume & issue
Vol. 2, no. 3

Abstract

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Burkitt lymphoma (BL) is a highly aggressive B cell lymphoma, presenting in extranodal sites or as an acute leukemia. Three clinical variants of BL are recognized: endemic BL, sporadic BL and immunodeficiency associated BL. Sporadic BL is seen worldwide, mainly in children and young adults involving the abdominal organs mostly the ileocaecal area. Pancreatic involvement is rare. The authors report a unique case of abdominal Burkitt lymphoma, initially diagnosed and treated as acute pancreatitis. Clinically, the patient presented severe abdominal pain and vomiting. Imaging findings were suggestive of inflammatory involvement of the pancreas, heading treatment towards this hypothesis. Unfortunately, the patient died during the diagnostic work up, and the autopsy findings demonstrated advanced Burkitt lymphoma with extensive involvement of pancreatic parenchyma and other organs within the abdominal cavity. Once Burkitt lymphoma is a potentially curable disease, early diagnosis is crucial for better outcomes.

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