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Tamoxifen- and Triptorelin-Induced Major Hypertriglyceridemia: A Case Report.
Widad Moussaoui1, Fatima Zahra Lahmamssi1, Hayat Aynaou1
1Department of Endocrinology, Diabetology, Metabolic Diseases and Nutrition, Hassan II University Hospital, Fez, MAR.
Tamoxifen and triptorelin treatment for breast cancer can cause severe hypertriglyceridemia. Lipid profile monitoring is crucial to manage these potentially fatal side effects.
Area of Science:
- Endocrinology
- Oncology
- Pharmacology
Background:
- Tamoxifen, a selective estrogen receptor modulator (SERM), is used in breast cancer treatment.
- Triptorelin, a gonadotropin-releasing hormone analog (GnRHa), is also employed in certain cancer therapies.
- Both medications have potential side effects impacting lipid metabolism.
Observation:
- A breast cancer patient developed severe hypertriglyceridemia (56 g/L), hypercholesterolemia (13 g/L), elevated LDL-C (4 g/L), and low HDL (0.25 g/L) after three months of tamoxifen and triptorelin treatment.
- The patient's oncologist discontinued the medications due to these adverse lipid changes.
Findings:
- Tamoxifen and triptorelin significantly altered the patient's lipid profile, leading to dangerous levels of triglycerides and cholesterol.
- Following treatment cessation and initiation of diet and fenofibrate, triglyceride levels normalized to 2 g/L within one month.
Implications:
- Tamoxifen and triptorelin can profoundly affect lipid metabolism, necessitating careful consideration of their benefit-risk balance.
- Regular monitoring of lipid profiles is essential for patients undergoing treatment with these medications to prevent severe complications like acute pancreatitis.
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