Abstract
Objective: To describe rare clinical and morphological forms of right ventricular neoplasms (mesenchymal hamartoma, rhabdomyoma) in infants which required surgical treatment in infancy.Methods: We performed 2 radical operations to remove right ventricular neoplasms: neonatal mesenchymal hamartoma and infantile rhabdomyoma.Results: We confirmed the effectiveness of surgery for rhabdomyoma and mesenchymal hamartoma in infants based on an 11-year postoperative follow-up period. We followed a necessary search strategy to detect tuberous sclerosis complex often associated with rhabdomyoma.Conclusion: Surgical treatment of rare right ventricular neoplasms in infants demonstrated favorable long-term results. Received 29 December 2022. Revised 22 February 2023. Accepted 27 March 2023. Informed consent: The patients' mothers informed consent to use the records for medical purposes is obtained. Funding: The study did not have sponsorship. Conflict of interest: The authors declare no conflict of interest. Contribution of the authorsLiterature review: E.A. Enin, A.V. MishinDrafting the article: A.V. MishinCritical revision of the article: K.N. Kuatbekov, E.A. Enin, A.L. Egizekov, A.A. SarsembayevaSurgical treatment: K.N. Kuatbekov, A.V. MishinFinal approval of the version to be published: K.N. Kuatbekov, E.A. Enin, A.L. Egizekov, A.V. Mishin, A.A. Sarsembayeva