Familial arachnoid cysts in association with autosomal dominant polycystic kidney disease
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Updated: Sep 30, 2026

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Published on: September 1, 2015
Füsun Korkmaz Alehan1, Berkan Gürakan, Muhteşem Ağildere
1Division of Child Neurology, Başkent University, Ankara, Turkey. falehan@hotmail.com
Insights
Autosomal dominant polycystic kidney disease (ADPKD) is linked to brain cysts. This report details a father and daughter with both ADPKD and posterior fossa arachnoid cysts, suggesting a potential familial connection.
Area of Science:
- Nephrology
- Neurology
- Genetics
Background:
- Autosomal dominant polycystic kidney disease (ADPKD) is a common genetic disorder.
- ADPKD is known for systemic manifestations, including intracranial aneurysms.
- Recent studies suggest an association between ADPKD and intracranial arachnoid cysts.
Purpose of the Study:
- To report a familial occurrence of posterior fossa arachnoid cysts in patients with autosomal dominant polycystic kidney disease.
- To highlight the potential association between ADPKD and arachnoid cysts in a family cohort.
Main Methods:
- Case report describing a father and daughter.
- Clinical and imaging data review for ADPKD and posterior fossa arachnoid cysts.
Main Results:
- Both father and daughter presented with asymptomatic ADPKD.
- Both individuals were diagnosed with a posterior fossa arachnoid cyst.
- This represents the first reported instance of familial arachnoid cysts associated with ADPKD.
Conclusions:
- The findings suggest a possible genetic link between ADPKD and the development of arachnoid cysts.
- Further research is warranted to explore the underlying mechanisms and prevalence of this association.
- This association may have implications for the clinical monitoring of ADPKD patients.
Abstract:
Autosomal dominant polycystic kidney disease (ADPKD) is a systemic disorder well-known for its association with intracranial aneurysms. Recently, intracranial arachnoid cysts have also been reported to be associated with ADPKD. We describe a father and daughter who each has a posterior fossa arachnoid cyst and asymptomatic ADPKD. To our knowledge, this is the first report of familial occurrence of arachnoid cysts in association with ADPKD.
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