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2007, Number 4

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Arch Cardiol Mex 2007; 77 (4)

Hypoplastic left ventricle syndrome. Report of a case in an adult woman

Miranda CI, Espínola ZN, Muñoz CL, Micheli A, Buendía HA, Zamora GC
Full text How to cite this article

Language: Spanish
References: 6
Page: 349-353
PDF size: 180.36 Kb.


Key words:

Hypoplastic left heart syndrome, Adult patient, Echocardiography.

ABSTRACT

Patients with hypoplastic left heart syndrome without surgery dye during the first year of life. In the literature there is only one report from our institution of a patient who survived to the second decade of life without surgery. The purpose of this work is to describe a case of a 24 years old female with hypoplastic left heart syndrome, who has survived until now in functional class I of New York Heart Association without surgery. In our patient, the survival is probably related with the presence of a ductus arteriosus, an interatrial septal defect and the secondary pulmonary arterial hypertension.


REFERENCES

  1. Tchervenkov CI, Jacobs ML, Tahta SA: Congenital Heart Surgery Nomenclature and Database Project: Hypoplastic Left Heart Syndrome. Ann Thorac Surg 2000; 69: S 170-9.

  2. Vargas Barrón J, Rijlaarsdam M, Romero Cárdenas A, Villegas M: Hypoplastic left heart syndrome: Report of a case of spontaneous survival to adulthood. Am Heart J 1992; 123: 1713-1719.

  3. Kirklin B, Kouchoukos N, Blackstone E, Doty D, Hanley F, Karp R: Cardiac Surgery. Morphology, diagnosis criteria, natural history, techniques, results and indications. Aortic atresia and other forms of hypoplastic left heart physiology. 3° Ed. Philadelphia USA. Elsevier, 2003, 1377-1400.

  4. Norwood WI, Lang P, Hansen DD: Physiologic repair of aortic atresia-hypoplastic left heart syndrome. N Engl J Med 1983; 308(1): 23-26.

  5. Deanfield J, Thaulow E, Warnes C, Webb G, Kolbel F, Hoffman A, et al: Management of grown up congenital heart disease. Eur Heart J 2003; 24: 1035-1084.

  6. Oechslin EN, Harrison DA, Connelly MS, Webb GD, Siu SC: Mode of death in adults with congenital heart disease. Am J Cardiol 2000; 86: 1111-1116.




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Arch Cardiol Mex. 2007;77