Acute Promyelocytic Leukemia and Brugada Syndrome: A Report on the Safety of Arsenic Trioxide/All-Trans-Retinoic Acid Therapy.
Giorgio RosatiSofia CamerloMatteo DalmazzoMelissa PadriniTiziano Tommaso BusanaMarco De GobbiAlessandro FornariAlessandro MorottiPublished in: Hematology reports (2023)
Acute promyelocytic leukemia (APL) is a rare and aggressive form of acute myeloid leukemia (AML). Instead of cytotoxic chemotherapy, a combination of all-trans-retinoic acid (ATRA) and arsenic trioxide (ATO) represents front-line therapy in low-risk patients. However, the therapeutic approach could be challenging in the case of a concomitant diagnosis of Brugada syndrome (BrS), a genetic disease characterized by an increased risk of arrhythmias and sudden cardiac death. Here, we present the case of a BrS patient who has been diagnosed with low-risk APL and treated with ATRA and ATO without observing arrhythmic events. In particular, we highlight the difficulties encountered by clinicians during the diagnostic work-up and the choice of the best treatment for these patients.
Keyphrases
- acute myeloid leukemia
- end stage renal disease
- newly diagnosed
- chronic kidney disease
- ejection fraction
- bone marrow
- liver failure
- peritoneal dialysis
- case report
- prognostic factors
- drinking water
- stem cells
- squamous cell carcinoma
- palliative care
- heavy metals
- radiation therapy
- patient reported outcomes
- genome wide
- patient reported
- hepatitis b virus
- copy number
- aortic dissection
- extracorporeal membrane oxygenation
- cell therapy
- rectal cancer