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A rare case report of corrected transposition of the great arteries in association with tuberous sclerosis and cardiac rhabdomyomas

Published online by Cambridge University Press:  19 November 2013

Rajiv Garg ,
Bhavesh Thakkar  and
Nilesh Oswal
Rajiv Garg*
Affiliation:
Department of Cardiology, U.N Mehta Institute of Cardiology and Research Center, Ahmedabad, Gujarat, India
Bhavesh Thakkar
Affiliation:
Department of Cardiology, U.N Mehta Institute of Cardiology and Research Center, Ahmedabad, Gujarat, India
Nilesh Oswal
Affiliation:
Department of Cardiology, U.N Mehta Institute of Cardiology and Research Center, Ahmedabad, Gujarat, India
*
Correspondence to: Dr R. Garg, U.N. Mehta Institute of Cardiology and Research Centre, Civil Hospital Campus, Ahmedabad-380016, Gujarat, India. Tel: 91 9712267685; Fax: 079 22682092; E-mail: d4drrajivgarg@gmail.com
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Abstract

The neuro-cutaneous syndrome tuberous sclerosis is commonly associated with rhabdomyomas in various organs including the heart. We are reporting a rare case of a 7-month old male child with congenitally corrected transposition of the great arteries associated with tuberous sclerosis and cardiac rhabdomyomas. To our knowledge, this rare association has not been reported so far.

Keywords

Tuberous sclerosisrhabdomyomascongenitally corrected transposition of the great arteries
Type
Brief Reports
Information
Cardiology in the Young , Volume 24 , Issue 5 , October 2014 , pp. 955 - 957
Copyright
Copyright © Cambridge University Press 2013 

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References

1. Ferencz, C, Rubin, JD, Mccarter, RJ, et al. Congenital heart disease: prevalence livebirth the Baltimore-Washington Infant Study. Am J Epidemiol 1985; 121: 31–36.CrossRefGoogle ScholarPubMed
2. Allwork, SP, Bentall, HH, Becker, AE, et al. Congenitally corrected transposition of the great arteries: morphologic study of 32 cases. Am J Cardiol 1976; 38: 910–923.Google Scholar
3. McKay, R, Anderson, RH, Smith, AJ. The coronary arteries in hearts with discordant atrioventricular connections. Thorac Cardiovasc Surg 1996; 111: 988–997.Google Scholar
4. Becker, AE. Primary heart tumors in the pediatric age group: a review of salient pathologic features relevant for clinicians. Pediatr Cardiol 2000; 21: 317–323.CrossRefGoogle ScholarPubMed
5. Elderkin, RA, Radford, DJ. Primary cardiac tumours in a paediatric population. J Pediatr Child Health 2002; 38: 173–177.CrossRefGoogle Scholar
6. Holley, DG, Martin, GR, Brenner, JI, et al. Diagnosis and management of fetal cardiac tumors: a multicenter experience and review of published reports. J Am Coll Cardiol 1995; 26: 516–520.Google Scholar
7. Smirniotopoulos, JG, Murphy, FM. The phakomatoses. AJNR Am J Neuroradiol 1992; 13: 725–746.Google ScholarPubMed
8. Farooki, ZQ, Ross, RD, Paridon, SM, et al. Spontaneous regression of cardiac rhabdomyoma. Am J Cardiol 1991; 67: 897–899.Google Scholar
9. Skinner, J, Hornung, T, Rumball, E. Transposition of great arteries: from fetus to adult. Heart 2008; 94: 1227–1235.Google Scholar
10. Huhta, JC, Danielson, GK, Ritter, DG, et al. Survival in atrioventricular discordance. Pediatr Cardiol 1985; 6: 57–60.Google Scholar