| Literature DB >> 28302247 |
Seyma Kayali1, Vehbi Dogan1, Nilüfer Arda2, Murat Koç3, Ilker Ertugrul1, Senem Özgür1, Utku Arman Örün1, Selmin Karademir1.
Abstract
Rhabdomyomas are the most common primary cardiac tumors, especially seen during early periods of childhood. Fetaltype rhabdomyoma is a benign tumor described almost always in extracardiac locations. Although the natural history of the cardiac rhabdomyoma is to regress, the behaviour of the fetal-type rhabdomyomas when present in the heart is unknown with respect to its infrequency. Herein, we report a hemodynamically unstable female neonate with a single large intra-cardiac mass unresponsive to medical treatment, who underwent surgery. The neonate could not survive the operation due to ventricular fibrillation. The mass was diagnosed as fetal-type cardiac rhabdomyoma on autopsy.Entities:
Mesh:
Year: 2017 PMID: 28302247
Source DB: PubMed Journal: J Coll Physicians Surg Pak ISSN: 1022-386X Impact factor: 0.711