Intracranial aneurysms in a child with autosomal recessive polycystic kidney disease

M I Lilova1, D L Petkov

  • 1Clinic of Pediatric Nephrology, University Childrens's Hospital, ul. Ianko Zabunov bl 40, 1408 Sofia, Bulgaria. Lilovss@iinf.bas.bg

Insights

Intracranial aneurysms (ICA) can occur in children with autosomal recessive polycystic kidney disease (ARPKD). Managing blood pressure is crucial for preventing hemorrhage in these patients.

Area of Science:

  • Nephrology
  • Neurology
  • Pediatrics

Background:

  • Autosomal dominant polycystic kidney disease is linked to intracranial aneurysms.
  • Intracranial aneurysms (ICA) are rarely reported in autosomal recessive polycystic kidney disease (ARPKD).

Observation:

  • A 2-year-old girl with ARPKD presented with hypertension, polyuria, polydipsia, and enuresis.
  • Imaging revealed multiple fusiform and saccular aneurysms in the middle and posterior cerebral arteries.
  • Liver showed cystic ectasia of biliary ducts; hypertension ranged from 140/100-170/120 mm Hg.

Findings:

  • Multiple intracranial aneurysms were identified in a pediatric patient with ARPKD.
  • The patient exhibited symptoms consistent with advanced kidney disease and severe hypertension.
  • Despite multiple aneurysms, the child remained neurologically asymptomatic during a 1.5-year follow-up.

Implications:

  • This case highlights that intracranial aneurysms can manifest in ARPKD patients.
  • Effective blood pressure control is vital for mitigating the risk of intracranial hemorrhage in ARPKD.
  • Early detection and management of hypertension are essential for pediatric ARPKD patients with vascular abnormalities.

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