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Published on: June 23, 2015
Intracranial aneurysms in a child with autosomal recessive polycystic kidney disease
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.
Abstract:
Intracranial aneurysms (ICA) are a well-known feature of autosomal dominant polycystic kidney disease. There is only one report about ICA in an adult patient with autosomal recessive polycystic kidney disease (ARPKD). We observed a 2-year, 6-month old girl with ARPKD and multiple ICA. The family history is negative for kidney disease. The diagnosis of ARPKD was based on the typical findings in ultrasonography and computed tomography. Cystic ectasia of biliary ducts 6.3/4.8 cm in diameter was found in the liver. Arterial hypertension in a range of 140/100-170/120 mm Hg was registered. The child has polyuria, polydipsia and enuresis. Blood urea was 15 mmol/l, creatinine in a range of 120 to 75 micromol/l. One episode of vomiting, dizziness and lethargy was the reason for a brain magnetic resonance imaging. Multiple fusiform and saccular aneurysms in the branches of middle and posterior cerebral arteries were seen bilaterally. The girl is growing well without neurological symptoms during an observation period of 1.5 years. Blood pressure is well controlled with an ACE inhibitor (Enalapril 2.5 mg daily). It was concluded that ICA can be found in patients with ARPKD. Blood pressure control is essential to reduce the risk of intracranial hemorrhage.
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