Cephalocele

Changed by Bruno Di Muzio, 14 Jun 2015

Updates to Article Attributes

Body was changed:

Cephalocoele refers to the outward herniation of CNS contents through a defect in the cranium. The vast majority are midline.

Epidemiology

The estimated incidence is 0.8-4:10,000 live births 13 with a well recognised geographical variation between sub types. Thee may be a greater female predilection 11.

Clinical presentation

  • content pending

Pathology

It is thought to arise due to failure of closure of the rostral end of the neuropore resulting from either overgrowth of neural tissue in the line of closure or a failure of induction by adjacent mesodermal tissues which in turn interfere with normal closure of the skull.

Sub typesSubtypes

There are two main subtypes:

Classification

Cephalocoeles can also be subclassified into 5 subtypes 15:

Location
Associations

Additional congenital anomalies may be present in up to 50 % of cases. They include

Markers:
  • maternal serum alpha fetoprotein (MSAFP) may be elevated

Radiographic features

Ultrasound

Sonographically, these lesions may appear as:

  • a cyst protruding from the fetal calvarium representing a meningocele or cyst within cyst appearance
  • a solid mass protruding from the calvarium representing a herniated brain: encephalocoele 
  • either or both of the above associated with a defect in the calvarium

Treatment and prognosis

The overall prognosis is variable dependent on severity and other associations (presence of hydrocephalus, microcephaly, etc). If a large cephalocoele is noted in an antenatal ultrasound scan it generally implicates a poor prognosis.

  • -<p><strong>Cephalocoele</strong> refers to the outward herniation of CNS contents through a defect in the cranium. The vast majority are midline.</p><h4>Epidemiology</h4><p>The estimated incidence is 0.8-4:10,000 live births <sup>13</sup> with a well recognised geographical variation between sub types. Thee may be a greater female predilection <sup>11</sup>.</p><h4>Pathology</h4><p>It is thought to arise due to failure of closure of the rostral end of the neuropore resulting from either overgrowth of neural tissue in the line of closure or a failure of induction by adjacent mesodermal tissues which in turn interfere with normal closure of the skull.</p><h5>Sub types</h5><p>There are two main subtypes:</p><ul>
  • +<p><strong>Cephalocoele</strong> refers to the outward herniation of CNS contents through a defect in the cranium. The vast majority are midline.</p><h4>Epidemiology</h4><p>The estimated incidence is 0.8-4:10,000 live births <sup>13</sup> with a well recognised geographical variation between sub types. Thee may be a greater female predilection <sup>11</sup>.</p><h4>Clinical presentation</h4><ul><li><em>content pending</em></li></ul><h4>Pathology</h4><p>It is thought to arise due to failure of closure of the rostral end of the neuropore resulting from either overgrowth of neural tissue in the line of closure or a failure of induction by adjacent mesodermal tissues which in turn interfere with normal closure of the skull.</p><h5>Subtypes</h5><p>There are two main subtypes:</p><ul>

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