Prenatally diagnosed large intrapericardial rhabdomyoma without haemodynamic compromise Authors Mehnaz Atiq Department of Paediatrics, Liaquat National Hospital and Medical Center, Karachi, Pakistan Durre Shahwar Department of Paediatrics, Liaquat National Hospital and Medical Center, Karachi, Pakistan Kashif Abbas Zaidi Department of Paediatrics, Liaquat National Hospital and Medical Center, Karachi, Pakistan DOI: https://doi.org/10.47391/JPMA.3558 Abstract Cardiac rhabdomyoma is the most common primary cardiac tumour and is considered to be a hamartoma of developing embryonic cardiac myocytes. It is commonly seen in tuberous sclerosis. The size and location of the tumour is the surrogate determinant of the risk of haemodynamic compromise. Pericardial rhabdomyoma is very rare and tends to follow the inherent natural history of spontaneous regression. We present cases of two foetuses diagnosed with large pericardial rhabdomyoma and no haemodynamic consequences. Key Words: Fetal cardiac tumors, intrapericardial rhabdomyoma, prenatal diagnosis. Downloads Full Text Article Published 2022-08-15 How to Cite Atiq, M., Durre Shahwar, & Kashif Abbas Zaidi. (2022). Prenatally diagnosed large intrapericardial rhabdomyoma without haemodynamic compromise. Journal of the Pakistan Medical Association, 72(9), 1855–1857. https://doi.org/10.47391/JPMA.3558 More Citation Formats ACM ACS APA ABNT Chicago Harvard IEEE MLA Turabian Vancouver Download Citation Endnote/Zotero/Mendeley (RIS) BibTeX Issue Vol. 72 No. 9 (2022): SEPTEMBER Section CASE SERIES