Autosomal dominant polycystic disease with associated arachnoid cysts and subdural cystic hygroma requiring shunting

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Familial arachnoid cysts in association with autosomal dominant polycystic kidney disease.

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...

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Chronic subdural haematoma and arachnoid cyst in autosomal dominant polycystic kidney disease (ADPKD).

We present the unusual association between chronic subdural haematoma (CSDH), intracranial arachnoid cyst and autosomal dominant polycystic kidney disease (ADPKD) in a 27-year-old man. CSDH is a documented complication of intracranial arachnoid cyst, the incidence of which is increased in patients with ADPKD. Awareness of this association may lead to earlier diagnosis of ADPKD and treatment of ...

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The Association Between Arachnoid Cysts and Subdural Hygroma and Spontaneous Resolution of Subdural Higroma

The association between arachnoid cyst and subdural hygroma (SH) is rare. We report a case, presenting of left middle cranial fossa arachnoid cyst with traumatic SH and spontaneous resolution of SH. The patient was totally asymtomatic prior to the injury and his arachnoid cyst was detected incidentally during investigations following minor head trauma. Our case with normal neurological examinat...

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Sacral radicular cysts in autosomal dominant polycystic kidney disease

This is the first report of a case of sacral radicular cysts in a patient with autosomal dominant polycystic kidney disease (ADPKD). A 46-year-old woman with ADPKD was found to have bilateral sacral radicular cysts discovered incidentally by magnetic resonance imaging (MRI). Cysts arising from arachnoid or spinal meningeal sac should be considered one of the manifestations of a more widespread ...

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Multiple cysts in the liver autosomal dominant polycystic liver disease.

A 45-year-old woman was admitted because of abdominal pain and a feeling of fullness. Ultrasound and CT scan of the abdomen showed a massively enlarged liver with hundreds of cysts and displacement of the right kidney. There were no cysts in the kidneys. Because several members of her family also had multiple cysts in the liver, the diagnosis of autosomal dominant polycystic liver disease (PCLD...

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ژورنال

عنوان ژورنال: Journal of Perinatology

سال: 2010

ISSN: 0743-8346,1476-5543

DOI: 10.1038/jp.2010.67