Cardiac rhabdomyoma mimicking haemodynamics of hypoplastic left heart syndrome
(2014) In Acta Cardiologica 69(3). p.308-310- Abstract
- Cardiac rhabdonnyomas are rare and often regress spontaneously. However, the management of rhabdomyoma with severe inflow and outflow obstructions is a challenge. An infant with a massive left ventricular rhabdomyoma mimicking the haemodynamics of hypoplastic left heart syndrome is reported. Surgery could not be contemplated because the mitral valve leaflets and chordae were imbedded in the tumour mass. The arterial duct (AD) was kept open to perfuse the systemic circulation and palliations with pulmonary artery branch banding and AD stenting were planned. However; while waiting for spontaneous regression of the tumour, the child died of circulatory collapse when 4 weeks old.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/4941507
- author
- El-Segaier, Milad LU and Galal, Mohammed O.
- organization
- publishing date
- 2014
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Rhabdomyoma, spontaneous regression, mitral obstruction
- in
- Acta Cardiologica
- volume
- 69
- issue
- 3
- pages
- 308 - 310
- publisher
- Acta Cardiologica
- external identifiers
-
- wos:000346681300010
- scopus:84902765833
- pmid:25029876
- ISSN
- 0001-5385
- DOI
- 10.2143/AC.69.3.3027834
- language
- English
- LU publication?
- yes
- id
- 164c7e62-5243-46b0-82f2-b8a155d66f51 (old id 4941507)
- date added to LUP
- 2016-04-01 13:03:46
- date last changed
- 2022-01-27 17:06:32
@article{164c7e62-5243-46b0-82f2-b8a155d66f51, abstract = {{Cardiac rhabdonnyomas are rare and often regress spontaneously. However, the management of rhabdomyoma with severe inflow and outflow obstructions is a challenge. An infant with a massive left ventricular rhabdomyoma mimicking the haemodynamics of hypoplastic left heart syndrome is reported. Surgery could not be contemplated because the mitral valve leaflets and chordae were imbedded in the tumour mass. The arterial duct (AD) was kept open to perfuse the systemic circulation and palliations with pulmonary artery branch banding and AD stenting were planned. However; while waiting for spontaneous regression of the tumour, the child died of circulatory collapse when 4 weeks old.}}, author = {{El-Segaier, Milad and Galal, Mohammed O.}}, issn = {{0001-5385}}, keywords = {{Rhabdomyoma; spontaneous regression; mitral obstruction}}, language = {{eng}}, number = {{3}}, pages = {{308--310}}, publisher = {{Acta Cardiologica}}, series = {{Acta Cardiologica}}, title = {{Cardiac rhabdomyoma mimicking haemodynamics of hypoplastic left heart syndrome}}, url = {{http://dx.doi.org/10.2143/AC.69.3.3027834}}, doi = {{10.2143/AC.69.3.3027834}}, volume = {{69}}, year = {{2014}}, }