Korean Circ J.  2013 Jan;43(1):54-56. 10.4070/kcj.2013.43.1.54.

A Case of Congenital Hypertrophic Cardiomyopathy

Affiliations
  • 1Department of Pediatrics, Korea University Hospital, Seoul, Korea. jgynhg@naver.com

Abstract

Congenital hypertrophic cardiomyopathy (HCMP) is a very rare congenital heart disease. Here, we report a case of neonatal HCMP, which was confirmed by two-dimensional echocardiography and autopsy. The HCMP rapidly progressed and the patient's condition deteriorated, despite the treatment for congestive heart failure.

Keyword

Cardiomyopathy, hypertrophic; Newborns

MeSH Terms

Autopsy
Cardiomyopathy, Hypertrophic
Echocardiography
Heart Diseases
Heart Failure
Humans
Infant, Newborn

Figure

  • Fig. 1 The echocardiography showed severe hypertrophy of both ventricles and ventricular septum (A) and color Doppler echocardiogram also demonstrated an accelerated flow at the outflow tract of the left ventricle (B).

  • Fig. 2 The gross specimen of the heart showed massive hypertrophy of both ventricles and microscopic examination demonstrated myofiber hypertrophy with nuclear enlargement (bar=50 µm).


Cited by  1 articles

Hypertrophic Cardiomyopathy in Infants from the Perspective of Cardiomyocyte Maturation
Heeyoung Seok, Jin-Hee Oh
Korean Circ J. 2021;51(9):733-751.    doi: 10.4070/kcj.2021.0153.


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