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Perindopril/amlodipine-induced thrombotic microangiopathy
Vlatka Periša1,2, Dorian Laslo2, Lana Maričić2,3
1Department of Hematology, University Hospital Centre Osijek, Croatia.
This case report details the first instance of perindopril/amlodipine causing thrombotic microangiopathy (TMA) syndrome. Prompt recognition and drug cessation led to full recovery, highlighting the importance of identifying drug-induced TMA.
Area of Science:
- Nephrology
- Hematology
- Pharmacology
Background:
- Thrombotic microangiopathy (TMA) is a rare but serious condition.
- Perindopril/amlodipine is a common antihypertensive medication.
- Drug-induced TMA is a recognized, albeit infrequent, adverse effect of some medications.
Observation:
- A 48-year-old female presented with rash, hematuria, weakness, hemiparesis, somnolence, and aphasia.
- Laboratory results indicated microangiopathic hemolytic anemia and thrombocytopenia.
- Symptoms emerged shortly after initiating perindopril/amlodipine therapy.
Findings:
- The patient was diagnosed with perindopril/amlodipine-induced thrombotic microangiopathy (TMA).
- The clinical presentation and timing suggested an acute, immune-mediated drug reaction.
- Hematologic abnormalities are rare but documented side effects of perindopril/amlodipine.
Implications:
- This is the first reported case of perindopril/amlodipine-induced TMA.
- Prompt diagnosis and withdrawal of the offending drug, alongside treatment (plasma exchange, corticosteroids), can lead to full recovery.
- Clinicians should consider TMA in patients presenting with relevant symptoms after starting perindopril/amlodipine.
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