Literature DB >> 28302247

Symptomatic Fetal-Type Cardiac Rhabdomyoma.

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.

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Year:  2017        PMID: 28302247

Source DB:  PubMed          Journal:  J Coll Physicians Surg Pak        ISSN: 1022-386X            Impact factor:   0.711


  1 in total

Review 1.  Recurrent primary endobronchial fetal rhabdomyoma: a case report and literature review.

Authors:  Stefano Marletta; Anna Caliò; Adele Fioravanzo; Enrico Cavallo; Evelin Torresani; Federica Zampieri; Eliana Gilioli
Journal:  Pathologica       Date:  2021-12
  1 in total

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