Pulmonary hypertension in a child with juvenile-type autosomal recessive polycystic kidney disease

J Korean Med Sci. 1999 Aug;14(4):451-4. doi: 10.3346/jkms.1999.14.4.451.

Abstract

An 11 year-old girl, whose condition was diagnosed as juvenile-type autosomal recessive polycystic kidney disease (ARPKD) at five years of age, presented with chest pain and dyspnea that had developed suddenly two months previously. Two-dimensional echocardiography, Doppler study and cardiac catheterization confirmed pulmonary hypertension. The underlying mechanism of the diagnosis was not defined. Two and a half months after the onset of symptoms, the patient died of pulmonary hypertensive crisis. Careful regular checks of cardiopulmonary status using two-dimensional echocardiography and Doppler should be considered for the early detection of pulmonary hypertension even in an asymptomatic patient with juvenile-type ARPKD.

Publication types

  • Case Reports

MeSH terms

  • Biopsy
  • Child
  • Echocardiography, Doppler
  • Fatal Outcome
  • Female
  • Humans
  • Hypertension, Pulmonary / complications*
  • Hypertension, Pulmonary / diagnostic imaging
  • Liver Cirrhosis / complications
  • Liver Cirrhosis / pathology
  • Polycystic Kidney, Autosomal Recessive / complications*
  • Polycystic Kidney, Autosomal Recessive / diagnostic imaging