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Hydrocephalus

By Stephen J. Falchek, , Nemours/Alfred I DuPont Hospital for Children;Thomas Jefferson University

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Hydrocephalus is accumulation of excessive amounts of CSF, causing cerebral ventricular enlargement and/or increased intracranial pressure. Manifestations can include enlarged head, bulging fontanelle, irritability, lethargy, vomiting, and seizures. Diagnosis is by ultrasonography in neonates and young infants with an open fontanelle and by CT or MRI in older infants and children. Treatment ranges from observation to surgical intervention, depending on severity and progression of symptoms.

Hydrocephalus is the most common cause of abnormally large heads in neonates. Hydrocephalus that develops only after the fontanelles have closed does not increase head circumference or cause the fontanelle to bulge but can markedly and rapidly increase intracranial pressure.

Etiology

Hydrocephalus can result from

  • Obstruction of CSF flow (obstructive hydrocephalus)

  • Impaired resorption of CSF (communicating hydrocephalus)

It can be either congenital or acquired from events during or after birth.

Obstruction most often occurs in the aqueduct of Sylvius but sometimes at the outlets of the 4th ventricle (Luschka and Magendie foramina). The most common causes of obstructive hydrocephalus are

  • Aqueductal stenosis

  • Dandy-Walker malformation

  • Chiari II type malformation

Aqueductal stenosis is narrowing of the outflow pathway for CSF from the 3rd ventricle to the 4th ventricle. It may be either primary, or secondary to scarring or narrowing of the aqueduct resulting from a tumor, hemorrhage, or infection. Primary aqueductal stenosis may involve true stenosis (forking of the aqueduct into smaller, poorly functioning channels) or presence of a septum in the aqueduct. Primary aqueductal stenosis may be inheritable; there are many genetic syndromes, some which are x-linked (thus male infants inherit the condition from otherwise unaffected mothers).

Dandy-Walker malformation is progressive cystic enlargement of the 4th ventricle.

In Chiari II type (formerly Arnold-Chiari) malformation, hydrocephalus occurs with spina bifida (see Spina Bifida ) and syringomyelia (see Syrinx of the Spinal Cord or Brain Stem ). Significant elongation of the cerebellar tonsils in Chiari type I or midline vermis in Chiari type II causes them to protrude through the foramen magnum, with beaking of the colliculi and thickening of the upper cervical spinal cord.

Impaired resorption in the subarachnoid spaces usually results from meningeal inflammation, secondary either to infection or to blood in the subarachnoid space, resulting from either subarachnoid or intraventricular hemorrhages, which are complications of delivery, particularly in premature infants (see Intracranial Hemorrhage).

Symptoms and Signs

Neurologic findings depend on whether intracranial pressure is increased, symptoms of which in infants include irritability, high-pitched cry, vomiting, lethargy, strabismus, and bulging fontanelle. Older, verbal children may complain of headache, decreased vision, or both. Papilledema is a late sign of increased intracranial pressure; its initial absence does not exclude hydrocephalus.

Consequences of chronic hydrocephalus may include precocious puberty in girls, learning disorders (eg, difficulties with attention, information processing, and memory), loss of vision, and impaired executive function (eg, problems with conceptualizing, abstracting, generalizing, reasoning, and organizing and planning information for problem-solving).

Diagnosis

  • Prenatal ultrasonography

  • Neonates: Cranial ultrasonography

  • Older infants and children: CT or MRI

Diagnosis is often made by routine prenatal ultrasonography. After birth, diagnosis is suspected if routine examination reveals an increased head circumference; infants may have a bulging fontanelle or widely separated cranial sutures. Similar findings can result from intracranial, space-occupying lesions (eg, subdural hematomas, porencephalic cysts, tumors). Macrocephaly may result from an underlying brain problem (eg, Alexander disease or Canavan disease), or it may be a benign, sometimes inherited, feature characterized by an increased amount of CSF surrounding a normal brain. Children suspected of having hydrocephalus require cranial imaging by CT, MRI, or ultrasonography (if the anterior fontanelle is open). Cranial CT or ultrasonography is used to monitor progression of hydrocephalus once an anatomic diagnosis has been made. If seizures occur, an EEG may be helpful.

Treatment

  • Sometimes observation or serial lumbar punctures

  • For severe cases, a ventricular shunt procedure

Treatment depends on etiology, severity, and whether hydrocephalus is progressive (ie, size of the ventricles increases over time relative to the size of the brain). Mild, nonprogressive cases may be observed with serial imaging studies and measurement of head size. To temporarily reduce CSF pressure in infants, ventricular taps or serial lumbar punctures (if the hydrocephalus is communicating) may be used.

Progressive hydrocephalus usually requires a ventricular shunt. Shunts typically connect the right lateral ventricle to the peritoneal cavity or, rarely, to the right atrium via a plastic tube with a one-way, pressure-relief valve. When a shunt is first placed in an infant or older child whose fontanelle is closed, rapid withdrawal of fluid can cause subdural bleeding as the brain shrinks away from the skull. When the fontanelles are open, the skull can decrease in circumference to match the decrease in brain size; thus, some clinicians recommend an early decision regarding shunt placement so that it can be done before fontanelle closure.

In a third ventriculostomy, an opening is created endoscopically between the 3rd ventricle and the subarachnoid space, allowing CSF to drain. This procedure is often combined with ablation of the choroid plexus and is becoming more commonly used in the US. It is particularly useful in less developed countries where access to consistent neurosurgical care is often limited. In certain cases (eg, hydrocephalus caused by primary aqueductal stenosis), third ventriculostomy may be adequate primary treatment.

A ventricular shunt that goes to the subgaleal space may be used in infants as a temporary measure for patients who may not require a more permanent shunt.

Although some children do not need the shunt as they age, shunts are rarely removed because of the risk of bleeding and trauma. Fetal surgery to treat congenital hydrocephalus has not been successful.

Shunt complications

The type of ventricular shunt used depends on the neurosurgeon’s experience, although ventriculoperitoneal shunts cause fewer complications than ventriculoatrial shunts. Shunt complications include

  • Infection

  • Malfunction

Any shunt has a risk of infection. Manifestations include chronic fever, lethargy, irritability, headache, or a combination and other symptoms and signs of increased intracranial pressure; sometimes redness becomes apparent over the shunt tubing. Antibiotics effective against the organism infecting the shunt, which may include skin flora, are given, and typically the shunt must be removed and replaced.

Shunts can malfunction because of a mechanical obstruction (typically blockage at the ventricular end) or because of fracture of the tubing. In either case, intracranial pressure can increase, which, if sudden, can be a medical emergency. Children present with headache, vomiting, lethargy, irritability, esotropia, or paralysis of upward gaze. Seizures may occur. If the obstruction is gradual, more subtle symptoms and signs can occur, such as irritability, poor school performance, and lethargy, which may be mistaken for depression. To assess shunt function, a shunt series (x-rays of the shunt tubing) and neuroimaging studies are done. The ability to compress the bulb that is present on many shunt systems is not a reliable sign of shunt function.

After the shunt is placed, head circumference and development are assessed, and imaging is done periodically.

Key Points

  • Hydrocephalus is usually caused by obstruction to the normal flow of CSF but can be due to impaired resorption of CSF.

  • If the disorder occurs before the cranial sutures have fused, the head may be enlarged, with bulging fontanelles.

  • Neurologic symptoms develop mainly if intracranial pressure increases; infants may have irritability, high-pitched cry, vomiting, lethargy, and strabismus.

  • Diagnose using ultrasonography prenatally and in neonates; use MRI or CT for older children.

  • Treat with observation or serial lumbar punctures or a ventricular shunt procedure depending on the etiology and severity and progression of symptoms.

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* This is the Professional Version. *