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Published on: June 28, 2021
Multiple myeloma presenting as acute pancreatitis.
Shakti Bedanta Mishra1, Afzal Azim2, Arindam Mukherjee2
1Department of Critical Care Medicine, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Raebareli Road, Lucknow 226014, Uttar Pradesh, India.
This case highlights a rare instance of acute pancreatitis in a young adult, later diagnosed as multiple myeloma. It underscores the importance of considering uncommon presentations for this plasma cell disorder.
Area of Science:
- Internal Medicine
- Oncology
- Gastroenterology
Background:
- Multiple myeloma (MM) is a plasma cell malignancy typically affecting older adults (>60 years).
- Classic MM symptoms include anemia, bone pain, and elevated erythrocyte sedimentation rate.
- Hypercalcemia is a known complication of MM, but acute pancreatitis is an infrequent manifestation.
Observation:
- A 36-year-old male presented with severe epigastric pain, nausea, vomiting, diarrhea, anorexia, respiratory distress, shock, and fever.
- Initial diagnosis was acute pancreatitis with hypercalcemia, thrombocytopenia, and elevated creatinine.
- Abdominal CT revealed lytic bone lesions and pancreatic necrosis, prompting further investigation.
Findings:
- Bone marrow biopsy confirmed multiple myeloma.
- This case represents an atypical presentation of multiple myeloma in a significantly younger patient.
- The patient's presentation mimicked severe acute pancreatitis, obscuring the underlying malignancy initially.
Implications:
- This case emphasizes the need to consider multiple myeloma in younger patients presenting with unexplained acute pancreatitis, especially when accompanied by hypercalcemia and bone lesions.
- It expands the spectrum of clinical presentations for multiple myeloma.
- Early recognition of rare MM manifestations is crucial for timely diagnosis and management, even in atypical demographics.
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