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Published on: April 22, 2019
An Atypical Presentation of Sporadic Jejunal Burkitt's Lymphoma
Pratik Naik1, James Wang2, Michael J Brazeau1
1Department of Internal Medicine, William Beaumont Army Medical Center (WBAMC), 5005 North Piedras Street, El Paso, TX 79920, USA.
Insights
A rare case of primary gastrointestinal lymphoma, Burkitt's lymphoma, was diagnosed in a young male presenting with anemia. Surgical resection followed by chemotherapy led to complete remission.
Area of Science:
- Oncology
- Gastroenterology
- Hematology
Background:
- Burkitt's lymphoma is an aggressive B-cell non-Hodgkin lymphoma (NHL).
- Primary gastrointestinal lymphoma is an uncommon presentation.
- Symptomatic anemia can be an initial indicator of gastrointestinal malignancy.
Purpose of the Study:
- To report a rare case of jejunal Burkitt's lymphoma presenting as symptomatic anemia.
- To highlight the diagnostic challenges and successful management of primary gastrointestinal Burkitt's lymphoma.
Main Methods:
- A 24-year-old male with symptomatic anemia underwent diagnostic evaluations including colonoscopy, EGD, and capsule endoscopy.
- Push enteroscopy was utilized for tissue biopsy of a jejunal mass.
- Immunohistochemical stains and PET/CT scan were performed for diagnosis and staging.
Main Results:
- Capsule endoscopy revealed an ulcerated jejunal mass.
- Biopsy confirmed Burkitt's lymphoma.
- PET/CT showed isolated jejunal involvement.
- The patient achieved complete remission after surgical resection and chemotherapy.
Conclusions:
- Jejunal Burkitt's lymphoma can present atypically with anemia.
- Multimodal imaging and endoscopic techniques are crucial for diagnosis.
- A combined approach of surgical resection and chemotherapy is effective for jejunal Burkitt's lymphoma.
Abstract:
Burkitt's lymphoma is a very aggressive type of B-cell NHL with replication approaching 100%. Primary gastrointestinal lymphoma is rare. In our case, a 24-year-old male initially presented with symptomatic anemia. He was initially evaluated with colonoscopy and EGD, both of which were unremarkable. A capsule endoscopy was then performed to further evaluate his significant anemia which revealed friable inflamed ulcerated mass in the jejunum. A push enteroscopy was then performed to obtain tissue from the jejunal mass. Biopsy results and immunohistochemical stains were consistent with Burkitt's lymphoma. PET/CT scan revealed only jejunal involvement. Treatment consisted of bowel resection prior to chemotherapy due to concern for perforation with chemotherapy. Patient achieved complete remission after the treatment.
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