1. Developmental (Congenital) Abnormalities of the Nervous System

2. Developmental (Congenital) Abnormalities of the Nervous System
Arachnoid Cysts
Encephaloceles
Craniosynostosis
Chiari malformation
Spinal Dysraphism

3. Arachnoid Cysts:
These are fluid filled intracranial mass lesions formed by splitting of the arachnoid membrane.

4. Around one-half are located in the Sylvian fissure.
Arachnoid Cysts:
The sites of Arachnoid Cysts:
Around one-half are located in the Sylvian fissure.
Cerebellopontine angle.
Suprasellar region.
Posterior fossa regions.

5. Sylvian Fissure Arachnoid Cyst

6. Cerebellopontine angle arachnoid cyst

7. Suprasellar Arachnoid Cyst

8. Posterior Fossa Aracnoid cyst

9. Arachnoid Cysts: They often present in paediatric age group.
Presentations:
They often present in paediatric age group.
Some remain asymptomatic.
Others enlarge in size causing a mass effect.
Others may present with haemorrhage.

10. Arachnoid Cysts:
Investigations:
CT Brain
MRI Brain

11. Arachnoid Cysts: Conservative: by observation and follow up.
Treatment:
Conservative: by observation and follow up.
Surgery: reserved only for symptomatic cases.
Surgical options include:
Endoscopy and fenestration into a cistern or ventricle.
Shunting: e.g. cystoperitoneal shunt.

12. They occur with a frequency of approximately 1-4 in 1000 births.
Encephaloceles:
These are developmental herniation of cerebral tissue through a cranial defect.
They occur with a frequency of approximately 1-4 in 1000 births.

13. Occipital Nasofrontal Frontoethmoidal Basal. Encephaloceles:
Sites: they may be:
Occipital
Nasofrontal
Frontoethmoidal
Basal.

14. Occipital Encephalocele

15. Occipital Encephalocele

16. Nasofrontal Encephalocele

17. Nasoethmoidal Encephalocele

18. Basal Encephalocele

19. Prevent infection. Reconstruct the skull. Encephaloceles:
Treatment: Surgical repair in order to:
Prevent infection.
Reconstruct the skull.

20. Craniosynostosis: These are premature fusion of the cranial sutures.
They may affect single or multiple sutures.
Premature fusion leads to restricted growth of the head resulting in presentation with an abnormal head shape.

21. Craniosynostosis: Types of Craniosynostosis:
Sagittal synostosis causes a narrow boat shaped head with frontal and occipital bossing (Scaphocephaly).
Bicoronal synostosis causes a shortened forehead (Brachycephaly).
Metopic synostosis causes Trigonocephaly.

22. Scaphocephaly

23. Scaphocephaly

24. Scaphocephaly

25. Brachycephaly

26. Brachycephaly

27. Trigonocephaly

28. Trigonocephaly

29. Diagnosis by CT brain with bone window.
Craniosynostosis:
Diagnosis by CT brain with bone window.
Surgical Treatment aimed at:
Correction of deformity.
Prevent the development of raised intracranial pressure.

30. Chiari malformation: Called also Arnold-Chiari Malformations:
Herniation of posterior fossa contents (e.g. cerebellar tonsils) through the foramen magnum.
Normally up to 5mm of tonsillar descent through the foramen magnum.

31. Normally up to 5mm of tonsillar descent through the foramen magnum.
Chiari malformation:
Normally up to 5mm of tonsillar descent through the foramen magnum.
Chiari I: >5 mm of tonsillar descent.
Chiari II: descent of the tonsils and cerebellar vermis.

32. Chiari malformation Type I

33. Chiari malformation Type II

34. Chiari malformation: Presentations:
Chiari I Malformation present in young adults with headache, exacerbated by coughing and straining.
Chiari II malformation present in infancy with signs of brainstem compression such as poor feeding, stridor and apnoeic spells.

35. Chiari malformation: Treatment of Chiari malformation include:
Treatment of associated Hydrocephalus, and then
Foramen magnum decompression.

36. DEVELOPMENTAL (CONGENITAL) ANOMALIES OF THE SPINES SPINA BIFIDA (SPINAL DYSRAPHISM)

37. SPINA BIFIDA Definition:
This is the most common developmental anomaly affecting the spinal column, and it means failure of the neural tube to close fully, so there is split or open spine.

38. SPINA BIFIDA

39. Types of spina bifida: Spina bifida Occulta Spina bifida Cystica
Spina bifida Aperta

40. Normal Spine

41. SPINA BIFIDA
Spina bifida Occulta:
The posterior vertebral arch has a defect within it, but there is no herniation of the neural tube.
This defect is found in 10% of the population.
On the skin over the defect various skin changes may be seen, e.g. hairy patch, an area of pigmentation, a fatty lump or a dermal sinus.

42. Spina bifida occulta

43. Spina bifida Occulta

44. SPINA BIFIDA 2. Spina bifida Cystica:
In this situation there is skin covering the defect making a cyst like.
If this cyst contains CSF only it is called MENINGOCELE.
If there is neural tissue within the sac, it is called MYELOMENINGOCELE.

45. Meningocele

46. MENINGOCELE

47. MYELOMENINGOCELE

48. MYELOMENINGOCELE

49. SPINA BIFIDA 3. Spina bifida Aperta:
The neural tube is open with no skin coverage, through a defect in the posterior vertebral arch.
CSF leakage usually occurs so there is a high risk of meningitis.

50. Spina bifida Aperta

51. Spina bifida Aperta

52. SPINA BIFIDA Aetiology: 90% of cases occur sporadically.
Hereditary factors: children of parents with spina bifida have a 5% risk of having the condition.
Dietary factors: folic acid administration during pregnancy may lower its incidence.
Some Anticonvulsants medications.

53. SPINA BIFIDA Clinical Features: Antenatal screening:
Post-delivery: General features
Spina bifida occulta:
Meningocele:
Myelomeningocele:

54. SPINA BIFIDA
Antenatal screening: by using:
Detection of alpha-fetoprotein in blood or in amniotic fluid obtained by amniocentesis.
The use of ultrasound.
Both tests allow the detection of such defects in over 80% of embryos with open neural tube .

55. Antenatal screening

56. Antenatal screening

57. SPINA BIFIDA b. Post-delivery: General features include:
The incidence is ranging from 1 to 8 per 1000 of the population.
Most problems tend to occur in the lumbosacral area and are associated with changes in bladder and bowel functions.
The higher the lesion the more sever the defect.
If the lesion is open then there is associated risk of meningitis.
Other associated disorders include Arnold-Chiari malformations type II, and in up to 80% hydrocephalus.

58. Myelomeningocele+ Hydrocephalus

59. SPINA BIFIDA c. Spina bifida occulta:
Usually asymptomatic. Accidental finding in X-rays.
Lipoma, skin dimple or a tuft of hair over the bifid spine.
Rarely urinary incontinence starting at adolescence.

60. SPINA BIFIDA d. Meningocele: No neurological manifestations.
Cystic translucent swelling with an expansible impulse on coughing.
The swelling is compressible.

61. Meningocele

62. Meningocele

63. Meningocele

64. Meningocele

65. SPINA BIFIDA e. Myelomeningocele:
Paraplegia, wasting, or contractures, with sensory loss.
Trophic disturbances are marked, especially perforating ulcers of foot.
Other congenital anomalies associated, mainly hydrocephalus.

66. Myelomeningocele

67. Myelomeningocele

68. Myelomeningocele

69. SPINA BIFIDA Investigations:
Head circumference measurement to check for an associated hydrocephalus.
Plain radiograph of the spine.
Ultrasound of the brain to exclude hydrocephalus.
CT and/or MRI brain to rule out hydrocephalus.

70. SPINA BIFIDA Treatment:
Spina bifida occulta requires no treatment in the majority of cases.
In the other forms of open spina bifida surgery should be performed as early as possible, and include:
Closure of the defect as early as possible to avoid meningitis.
The hydrocephalus needs immediate shunting even prior to closure of the defect of spina bifida.

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