ArticleJournal of surgical case reports2018
Burkitt's lymphoma presenting as acute appendicitis: a case report.
Article in Journal of surgical case reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 8 citations in OpenAlex.
- Article
- A Case of Appendicitis Due to Burkitt Lymphoma Masking the Systemic Symptoms of Rapidly Progressing Burkitt Lymphoma.Surgical case reports · 2025Article
- Burkitt lymphoma presenting as cecum mass and spontaneous tumor lysis syndrome with hypercalcemia.Clinical case reports · 2023Article
- Double-Expressor Appendiceal Burkitt's Lymphoma: A Case Report and Literature Review.Case reports in hematology · 2022Article
- Burkitt-type lymphoma incidentally found as the cause of acute appendicitis: a case report and review of literature.Surgical case reports · 2021Article
- Burkitt Leukemia Presenting as Acute Appendicitis: A Case Report and Literature Review.The American journal of case reports · 2020Review
Corrections and comments
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Authors and funding
6 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Appendiceal lymphomas are exceedingly rare, constituting around 0.015% of all gastrointestinal lymphoma cases. Burkitt's lymphoma is the second most prevalent pathology, diagnosed in 25.9% of patients. We report a case of a 36-year-old male admitted with acute abdominal pain with 2 days of evolution, localized in the right lower quadrant associated with hyporexia, but no fever. On examination he presented abdominal tenderness on the right iliac fossa. A diagnosis of acute appendicitis was made clinically. At the post-operative follow up, 2 weeks later, he presented a low back pain of high intensity, associated with swelling of the abdomen, night sweats, daily fevers and weight loss. The histopathological exam of the appendix revealed diffuse and transmural lymphoid proliferation. Immunohistochemistry suggested high grade B-cell lymphoma indicative of Burkitt's lymphoma. This patient was staged as a IVxB lymphoma and was submitted into polychemotherapy with a complete clinical response in 8 months.
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Registered trials
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