Skip to main content
Top
Published in: BMC Cardiovascular Disorders 1/2018

Open Access 01-12-2018 | Case report

Fatal heart failure caused by severe pulmonary regurgitation, tricuspid regurgitation and late-onset mitral stenosis in an adult patient with Noonan syndrome: a case report

Authors: Yoshito Kadoya, Tsuneaki Kenzaka, Yohei Oda, Satoaki Matoba

Published in: BMC Cardiovascular Disorders | Issue 1/2018

Login to get access

Abstract

Background

In patients with Noonan syndrome (NS), cardiac disorders such as pulmonary valve stenosis (PS) or hypertrophic cardiomyopathy (HCM) are common. While some patients can develop heart failure associated with HCM, the long-term outcome of adult patients with NS is reported to be good. Fatal outcomes of heart failure in patients with NS but without HCM are rare.

Case presentation

We report a 25-year-old Japanese woman diagnosed with NS in adulthood. She exhibited short stature and minor facial dysmorphism and was diagnosed with PS at 1 year of age. After surgical valvuloplasty for PS at 6 years of age, her general condition became stable without specific medical treatment. She discontinued regular medical follow-up for PS. At 21 years of age, she developed acute decompensated heart failure, which was mainly right-sided heart failure due to severe pulmonary regurgitation (PR) and tricuspid regurgitation (TR). There was no evidence of HCM or PS recurrence. On the basis of the history of PS and characteristic physical features including short stature, webbed neck, and hypertelorism, she was clinically diagnosed with NS. At 25 years of age, she developed heart failure of both sides due to PR, TR and late-onset severe mitral stenosis (MS). The etiology of MS was uncertain. Owing to the patient’s condition, surgical options were considered to be extremely high risk. She was treated with optimal medical treatment as well as the occasional abdominal cavity drainage for recurrent ascites; however, she died of decompensated heart failure at 27 years of age.

Conclusions

We describe an adult patient with NS without HCM who died of heart failure caused by severe PR, TR and MS. Clinicians should recognize that ongoing or late-onset cardiac disorders can develop in patients with NS, and lead to fatal heart failure. Optimal medical follow-up to monitor cardiac function and early identification of heart failure are important.
Literature
1.
go back to reference Noonan JA, Ehmke DA. Associated non-cardiac malformations in children with congenital heart disease. J Pediatr. 1963;63:468–70. Noonan JA, Ehmke DA. Associated non-cardiac malformations in children with congenital heart disease. J Pediatr. 1963;63:468–70.
2.
go back to reference Noonan JA. Hypertelorism with turner phenotype. A new syndrome with associated congenital heart disease. Am J Dis Child. 1968;116:373–80.CrossRefPubMed Noonan JA. Hypertelorism with turner phenotype. A new syndrome with associated congenital heart disease. Am J Dis Child. 1968;116:373–80.CrossRefPubMed
3.
4.
go back to reference Patton MA. Noonan syndrome: a review. Growth Genet Horm. 1994;33:1–3. Patton MA. Noonan syndrome: a review. Growth Genet Horm. 1994;33:1–3.
5.
go back to reference Shaw AC, Kalidas K, Crosby AH, Jeffery S, Patton MA. The natural history of Noonan syndrome: a long-term follow-up study. Arch Dis Child. 2007;92:128–32.CrossRefPubMed Shaw AC, Kalidas K, Crosby AH, Jeffery S, Patton MA. The natural history of Noonan syndrome: a long-term follow-up study. Arch Dis Child. 2007;92:128–32.CrossRefPubMed
7.
go back to reference Colquitt JL, Noonan JA. Cardiac findings in Noonan syndrome on long-term follow-up. Congenit Heart Dis. 2014;9:144–50.CrossRefPubMed Colquitt JL, Noonan JA. Cardiac findings in Noonan syndrome on long-term follow-up. Congenit Heart Dis. 2014;9:144–50.CrossRefPubMed
8.
go back to reference Calcagni G, Limongelli G, D'Ambrosio A, Gesualdo F, Digilio MC, Baban A, et al. Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results. Int J Cardiol. 2017;245:92–8.CrossRefPubMed Calcagni G, Limongelli G, D'Ambrosio A, Gesualdo F, Digilio MC, Baban A, et al. Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results. Int J Cardiol. 2017;245:92–8.CrossRefPubMed
9.
go back to reference Prendiville TW, Gauvreau K, Tworog-Dube E, Patkin L, Kucherlapati RS, Roberts AE, et al. Cardiovascular disease in Noonan syndrome. Arch Dis Child. 2014;99:629–34.CrossRefPubMed Prendiville TW, Gauvreau K, Tworog-Dube E, Patkin L, Kucherlapati RS, Roberts AE, et al. Cardiovascular disease in Noonan syndrome. Arch Dis Child. 2014;99:629–34.CrossRefPubMed
10.
go back to reference Hickey EJ, Mehta R, Elmi M, Asoh K, McCrindle BW, Williams WG, et al. Survival implications: hypertrophic cardiomyopathy in Noonan syndrome. Congenit Heart Dis. 2011;6:41–7.CrossRefPubMed Hickey EJ, Mehta R, Elmi M, Asoh K, McCrindle BW, Williams WG, et al. Survival implications: hypertrophic cardiomyopathy in Noonan syndrome. Congenit Heart Dis. 2011;6:41–7.CrossRefPubMed
11.
go back to reference Wilkinson JD, Lowe AM, Salbert BA, Sleeper LA, Colan SD, Cox GF, et al. Outcomes in children with Noonan syndrome and hypertrophic cardiomyopathy: a study from the pediatric cardiomyopathy registry. Am Heart J. 2012;164:442–8.CrossRefPubMed Wilkinson JD, Lowe AM, Salbert BA, Sleeper LA, Colan SD, Cox GF, et al. Outcomes in children with Noonan syndrome and hypertrophic cardiomyopathy: a study from the pediatric cardiomyopathy registry. Am Heart J. 2012;164:442–8.CrossRefPubMed
12.
go back to reference Noonan JA. Noonan Syndrome. In: Goldstein SR, Reynolds CR, editors. Handbook of neurodevelopmental and genetic disorders in adults. New York: The Guilford Press; 2005. p. 308–19. Noonan JA. Noonan Syndrome. In: Goldstein SR, Reynolds CR, editors. Handbook of neurodevelopmental and genetic disorders in adults. New York: The Guilford Press; 2005. p. 308–19.
13.
go back to reference Lin AE, Basson CT, Goldmuntz E, Magoulas PL, McDermott DA, McDonald-McGinn DM, et al. Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management. Genet Med. 2008;10:469–94.CrossRefPubMedPubMedCentral Lin AE, Basson CT, Goldmuntz E, Magoulas PL, McDermott DA, McDonald-McGinn DM, et al. Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management. Genet Med. 2008;10:469–94.CrossRefPubMedPubMedCentral
Metadata
Title
Fatal heart failure caused by severe pulmonary regurgitation, tricuspid regurgitation and late-onset mitral stenosis in an adult patient with Noonan syndrome: a case report
Authors
Yoshito Kadoya
Tsuneaki Kenzaka
Yohei Oda
Satoaki Matoba
Publication date
01-12-2018
Publisher
BioMed Central
Published in
BMC Cardiovascular Disorders / Issue 1/2018
Electronic ISSN: 1471-2261
DOI
https://doi.org/10.1186/s12872-018-0878-1

Other articles of this Issue 1/2018

BMC Cardiovascular Disorders 1/2018 Go to the issue