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Updated: Apr 3, 2026

From a 2DE-Gel Spot to Protein Function: Lesson Learned From HS1 in Chronic Lymphocytic Leukemia
Published on: October 19, 2014
CD5-positive diffuse large B-Cell lymphoma presenting with protein-losing enteropathy.
Kenji Moriwaki1, Hiro Tatetsu1, Yusuke Higuchi1
1Department of Hematology, Rheumatology and Infectious Diseases, Kumamoto University Hospital, Kumamoto, Japan.
A rare case of CD5-positive diffuse large B-cell lymphoma (DLBCL) in the small intestine caused protein-losing enteropathy. Chemotherapy and stem cell transplant led to remission, suggesting a distinct clinical entity.
Area of Science:
- Gastroenterology
- Hematology
- Oncology
Background:
- Gastrointestinal lymphoma is rare, but the GI tract is a common extranodal site for non-Hodgkin lymphoma.
- Diffuse large B-cell lymphoma (DLBCL) and mucosa-associated lymphoid tissue lymphoma frequently involve the stomach and small intestine.
- Protein-losing enteropathy (PLE) secondary to lymphoma is rare, especially when caused by CD5-positive DLBCL.
Purpose of the Study:
- To report a rare case of CD5-positive DLBCL presenting with PLE.
- To highlight the diagnostic and therapeutic approach for this unusual condition.
- To propose CD5-positive DLBCL with PLE as a distinct clinical entity.
Main Methods:
- Case report of a 60-year-old woman with refractory diarrhea and edema.
- Diagnostic workup including assessment of protein leakage and double-balloon endoscopy.
- Histopathological confirmation of de novo CD5-positive DLBCL.
Main Results:
- The patient was diagnosed with CD5-positive DLBCL of the small intestine.
- Hypoproteinemia with significant protein leakage in the colon and small intestine was identified.
- Treatment with DA-EPOCH-R chemotherapy resulted in prompt improvement and resolution of PLE.
Conclusions:
- CD5-positive DLBCL can present as PLE, a rare but distinct clinical entity.
- Prompt diagnosis and treatment with chemotherapy and stem cell transplantation are effective.
- Further research is warranted to confirm this as a separate clinical entity.
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