Cardiac rhabdomyoma often shows spontaneous regression and usually requires only close follow-up. However, patients with symptomatic inoperable rhabdomyomas may be candidates for everolimus treatment. Our patient had multiple inoperable cardiac rhabdomyomas causing serious left ventricle outflow-tract obstruction that showed a dramatic reduction in the size after everolimus therapy, a mammalian target of rapamycin (mTOR) inhibitor. After discontinuation of therapy, an increase in the diameter of masses occurred and everolimus was restarted. After 6 months of treatment, rhabdomyomas decreased in size and therapy was stopped. In conclusion, everolimus could be a possible novel therapy for neonates with clinically significant rhabdomyomas.
CITATION STYLE
Bornaun, H., Öztarhan, K., Erener-Ercan, T., Dedeoğlu, R., Tugcu, D., Aydoğmuş, Ç., … Kavuncuoglu, S. (2016). Regression of Cardiac Rhabdomyomas in a Neonate after Everolimus Treatment. Case Reports in Pediatrics, 2016, 1–3. https://doi.org/10.1155/2016/8712962
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