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This study aims to determine size of corpus callosum on midsagittal MR scan in patients with a pineal cyst and to compare it with the control group without a pineal cyst.
A pineal cyst (PC) is a benign affection of the pineal gland, its prevalence in population reaches 1-2 %. Etiopathogenesis of PC is unknown, several hypotheses have been proposed. One of the hypothesis consider perinatal hypoxia as a causative factor for a development of PC in later life. Ozmen et al. showed significantly higher prevalence of PC in patients with cerebral palsy (p<0.001). Bregant et al. studied presence of PC in patients that suffered from a mild to moderate perinatal hypoxia. Prevalence of PC reached 36 % in these patients and presence of PC was associated with a atrophy of the corpus callosum (p<0.005). The atrophy of the corpus callosum is considered to be a sign of a periventricular leukomalacia, i.e. an ischemic insult in a perinatal period.
In the present study, we are going to compare an area of corpus callosum on a midsagittal magnetic resonance T2-weighted scan in the group of patients with PC and in the control group without PC. The goal of the study is to determine if there is a relationship between atrophy of the corpus callosum and PC. Such finding would support abovementioned theory of etiopathogenesis of PC.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group of patients with pineal cyst | Group of patients with pineal cyst |
| |
| Control group | Group of subjects without pineal cyst |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MR of the brain | Diagnostic Test | MR of the brain without gadolinium, incl. T2-weighted image |
|
| Measure | Description | Time Frame |
|---|---|---|
| size of corpus callosum | size of corpus callosum in mm2 measured on the midsagittal T2-weighted MR scan | time of the MR examination |
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Inclusion Criteria:
Exclusion Criteria:
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| ID | Term |
|---|---|
| D002547 | Cerebral Palsy |
| ID | Term |
|---|---|
| D001925 | Brain Damage, Chronic |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
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