Skip to main content

Valvular Commitment in Hunter Syndrome

  • Chapter
  • First Online:
Cardiovascular Surgery

Abstract

A 30-year-old white male patient with a past history of rheumatic fever presented to the hospital with an exacerbation of a 6-month-old progressive dyspnea, accompanied by pallor and lipothymia. At the occasion, both mitral and aortic valves showed features compatible with rheumatic valvulopathy on echocardiographic assessment. Despite the severity of the valvular lesion, the patient refused to undergo surgical treatment, maintaining only spaced doses of benzathine penicillin.

The patient displays a series of deformities since his infancy, such as thoracic-wall dysmorphism (pectus excavatum), bilateral reduction of visual acuity, abnormal gait, and multiple permanent osteoarticular deformities. There was no cognitive deficit or developmental delay nor any report of another known case of genetic disease in the family. In spite of having undergone medical evaluations during childhood, no genetic testing or assessment was performed at the time.

At examination, he presented good general aspect, with preserved orientation of time/space; eupneic, with pink/red and hydrated mucosae; afebrile, anicteric; and acyanotic. His physical dysmorphisms comprised a large-bridged nose with a saddlelike morphology, rude facial expressions, a deformed dental arcade with short and protruding teeth, asymmetrical pectus excavatum and kyphoscoliosis with a right-sided deflection, long superior and inferior limbs with articular misalignment, rigidity, thick fingers, and a “claw-like” disposition of both hands. He presented a moving precordium, with a palpable ictus at the encounter of the 6th intercostal space and the anterior axillary line, and split of S2 along with a hyperphonesis of its pulmonary component. There was also a mesosystolic murmur in crescendo-decrescendo with fremitus that radiated to the neck at the aortic auscultation site. The abdomen presented a prominent and painful to touch hepatomegaly and splenomegaly, along with an inguinal herniation on the right side.

During follow-up, the patient eventually accepted to undergo cardiac surgery for valvular replacement.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 99.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 129.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Bibliography

  1. Cunningham M. T cell mimicry in inflammatory heart disease. Mol Immunol Feb. 2004;40(14–15):1121–7.

    Article  CAS  Google Scholar 

  2. Remenyi B, et al. Valvular aspects of rheumatic heart disease. Lancet. 2016;387(10025):1335–46.

    Article  Google Scholar 

  3. Neufeld E, Muenzer J. The mucopolysaccharidoses. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The metabolic and molecular bases of inherited disease. 8th ed. New York: McGraw- Hill; 2001. p. 3421–52.

    Google Scholar 

  4. Chen MR, Lin SP, Hwang HK, Yu CH. Cardiovascular changes in mucopolysaccharidoses in Taiwan. Acta Cardiol. 2005;60:51–3.

    Article  Google Scholar 

  5. Dangel JH. Cardiovascular changes in children with mucopolysaccharide storage diseases and related disorders: clinical and echocardiographic findings in 64 patients. Eur J Pediatr. 1998;157:534.

    Article  CAS  Google Scholar 

  6. Leal GN, de Paula AC, Leone C, Kim C. Echocardiographic study of paediatric patients with mucopolysaccharidosis. Cardiol Young. 2010;20:254–61.

    Article  Google Scholar 

  7. Burke AP. Pathology of Rheumatic Heart Disease; 2015. Available: http://emedicine.medscape.com/article/1962779-overview#a1. Upload: 15 Oct 2015.

  8. Braunlin EA, Harmatz PR, Scarpa M, Furlanetto B, Kampmann C, Loehr JP, Ponder KP, Roberts WC, Rosenfeld HM, Giugliani R. Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management. J Inherit Metab Dis. 2011;34:1183–97.

    Article  CAS  Google Scholar 

  9. Special Writing Group of the Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease of the Council on Cardiovascular Disease in the Young of the American Heart Association. Guidelines for the diagnosis of rheumatic fever. Jones Criteria, 1992 update. JAMA. 1992;268(15):2069–73. Erratum in: JAMA 1993 Jan 27;269(4):476.

    Google Scholar 

  10. Vahanian A, Alfieri O, Andreotti F. ESC/EACTS guidelines on the management of valvular heart disease. Eur Heart J. 2012. https://doi.org/10.1093/eurheartj/ehs109 & Eur J Cardiothorac Surg. https://doi.org/10.1093/ejcts/ezs455.

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2019 Springer Nature Switzerland AG

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Sampaio, M.X.C., Silva, P.G., Colonnezy, E.A.M., Júnior, R.A., Fernandes, A.M.S. (2019). Valvular Commitment in Hunter Syndrome. In: Almeida, R., Jatene, F. (eds) Cardiovascular Surgery. Springer, Cham. https://doi.org/10.1007/978-3-319-57084-6_37

Download citation

  • DOI: https://doi.org/10.1007/978-3-319-57084-6_37

  • Published:

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-57083-9

  • Online ISBN: 978-3-319-57084-6

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics