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Cerebrospinal fluid (CSF)

It is made in the choroid plexuses located at the base of the ventricles. A very small amount is also made by the ependymal cells lining the floor of the ventricles.

Total circulating volume is 50 ml in newborns and 150 ml in adults. CSF enters the general circulation from the superior sagittal sinus and is absorbed in the arachnoid villi and arachnoid granulation region.

It passes from the 4th ventricle to the spinal cord with 2 Luschka and 1 Magendi holes.

CSF tasks

Protects the brain from trauma.

It clears the residues of neuronal metabolism.

It acts as a reserve.

CSF pressure is 8-18 cm H2O, and 9-12 cmHp in newborns.

If the lactic acid level in CSF is above 30 mg, organic acidemia and mitochondrial myopathy are considered.

Measles antibodies are over 1/8 in SSPE. Antibodies to GM1 gangliosides can be demonstrated in Guillain-Barre.

The CSF/blood ratio of IgG is about 0.6. If this rate increases, CNS disease and collagen tissue diseases should be considered.

30% of the CSF protein is globulins. IgG/albumin=0.21. If this rate increases, multiple sclerosis, SSPE, neurosyphilis, postinfectious encephalomyelitis should be considered.

Causes of xanthochromic CSF

Subarachnoid hemorrhage (if hemorrhagic CSF is centrifuged, if the upper serum is yellow, it is subarachnoid hemorrhage, if it is clear, it is hemorrhagic because it is traumatic)

hyperbilirubinemia

carotenemia

Significantly elevated CSF protein (like tuberculosis)

LP contraindications

Findings suggestive of an intracranial mass or presence of an intracranial mass

Skin infection in the LP area

Platelet count <20,000 /mm3

hydrocephalus

It is an enlargement of the cerebral ventricles with excessive accumulation of CSF. It is the most common cause of head circumference enlargement in newborns. There are two types:

Causes of Communicated Hydrocephalus

Achondroplasia

basilar impression

Choroid plexus papilloma tumors

meningitis

Post hemorrhagic cases

Leukemic cell invasion into the subarachnoid space

Meningeal malignancy

Benign development of the subarachnoid space

Causes of Non-Communicated Hydrocephalus

Aquaductal stenosis

Arnold-Chiari malformation

Klippel-Feil syndrome

Dandy-Walker malformation

Mass lesions (abscess, hematoma, tumor)

vein of galen aneurysm

Walker-Warburg syndrome

Infection (toxoplasma, neurocysticercosis, mumps)

NF-1/2

LlCAM mutation

X bound/OD/OR

mitochondrial

Neurocutaneous diseases

The presence of abnormal head circumference increase and symptoms of CRPS, which constitute the clinical features, are diagnostic.

Although hydrocephalus can be diagnosed with CT, USG is useful if the anterior fontanelle is open.

The causes of hydrocephalus are related to the time of its occurrence. the most common causes in the prenatal period or in the first month of life; Congenital malformations such as intraventricular hemorrhage, infection or aqueductal stenosis.

Depending on the etiology, mannitol, acetazolamide, furosemide can be used in treatment. Serial lumbar punctures, CSF drainage from the fontanel (tap method) and external drainage applications can also be performed.

The best treatment method is ventriculoperitoneal shunt placement.

Increased Intracranial Pressure Syndrome (CIBAS)

In young children whose fontanelles are not closed, an increase in head diameter, wide-tense-pulsatile fontanel and open sutures are detected, while papilledema is rare.
Headache, vomiting, papilledema, sudden strabismus (6th cranial nerve compression) develop in older children with closed fontanelles. Hypertension and bradycardia occur.
In chronic CRPS, strabismus develops gradually, with a setting sun scene and prolonged intermittent vomiting. (example, tuberculous meningitis)
There is no difference between chronic and acute CRPS in infants. In chronic CIBAS, opening of the sutures, demineralization in the sella turcica, erosion in the posterior clinoids, and hammered copper appearance can be observed in the cranial radiographs. Fracture test sound (Macewen sign) may be obtained.

Some important causes of CRPS in children

Cerebral hypoxia (brain edema develops)
head injuries
Extradural (epidural) bleeding
Subdural bleeding
Craniosynostoses (may develop very slowly and be missed, optic atrophy-blindness-cortical atrophy may develop)
hydrocephalus
brain abscess
tumors

Benign Intracranial Hypertension (Pseudotumor Cerebri)

It is an increase in intracranial pressure without a mass occupying space in the head.

When the intracranial mass is excluded, LP is performed and the pressure is found to be high (>20 cm Hp in infants, >25 cmH2O in children, >28 cm in obese and sedentary children).

Due to prolonged papilledema, it may cause optic nerve damage and cause vision loss, and the enlarged blind spot in the vision test is an early finding.

It may very rarely cause herniation (manifested as a mass in the posterior fossa).

The most common finding is headache. Vomiting and diplopia due to 6th nerve palsy are common. The first affected cranial nerve is the 6th nerve.

In treatment, B05 pressure is lowered with LP. Acetazolamide and corticosteroids are used.

Etiology of pseudotumor cerebri in children


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