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Lactic acidosis: a unique presentation of diffuse large B-cell lymphoma
Turab Jawaid Mohammed1, Rohit Gosain2, Rajeev Sharma1
1Hematology/Oncology, Roswell Park Cancer Institute, Buffalo, New York, USA.
BMJ Case Reports
|October 27, 2019
Summary
A case study highlights diffuse large B-cell lymphoma (DLBCL) presenting as metabolic encephalopathy and lactic acidosis in an elderly patient. Prompt chemotherapy initiation led to significant improvement, emphasizing DLBCL in differential diagnoses.
Area of Science:
- Hematology
- Oncology
Background:
- Metabolic encephalopathy and lactic acidosis can present with diverse etiologies.
- Aggressive lymphomas, such as diffuse large B-cell lymphoma (DLBCL), should be considered in the differential diagnosis of unexplained metabolic derangements.
Observation:
- An elderly male presented with altered mental status, anemia, thrombocytopenia, elevated lactate dehydrogenase, and lactic acidosis.
- Imaging revealed significant lymphadenopathy, splenomegaly, and bilateral adrenal involvement.
- Bone marrow biopsy confirmed non-germinal center B-cell-like (non-GCB) DLBCL.
Findings:
- The patient's condition dramatically improved following prompt chemotherapy with a dose-adjusted regimen including etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, rituximab, and intrathecal methotrexate.
- This case underscores the importance of early diagnosis and aggressive treatment for DLBCL, even in critically ill patients.
Implications:
- Aggressive lymphomas like DLBCL can manifest with unusual symptoms, necessitating a broad differential diagnosis.
- Urgent chemotherapy initiation is crucial for improving outcomes in patients with DLBCL presenting with severe systemic illness, irrespective of initial performance status.
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