ULTRASOUND OF CALLOSAL AGENESIS

-         Complete agenesis

-         Partial agenesis 

The corpus callosum is a thin band of white matter, which is difficult to demonstrate sonographically. It is only well visualized on mid-sagittal or mid-coronal views of the brain and requires optimal angles of insonation to demonstrate.
 

COMPLETE AGENESIS OF THE CORPUS CALLOSUM

                                                                                                          

 

 

 

 

 

Interhemispheric cyst,high-riding 3rd ventricle

 

 

 

Sunburst appearance of gyri

 

 

 

 Interhemispheric cyst,high-riding 3rd ventricle

 

 

 

 

 

Colpocephaly

 

 

 

Interhemispheric fissure adjoins the 3rd ventricle

 

 

 

 

Colpocephaly (dilatation of the occipital horn of the lateral ventricle).

 

 

Callosal Agenesis – absent cingulated gyrus and pericallosal artery

Normal Corpus Callosum – normal pericallosal artery

 

 

Normal cingulate gyral pattern.

Dysgenesis of the cingulate gyrus with characteristic radial orientation of the sulci

Normal corpus callosum, pericallosal (PC) and callosomarginal (CM)arteries.

Agenesis of the corpus callosum with a "sunburst" gyral pattern and non visualization of the pericallosal or callosomarginal arteries

 

 

Postnatal MRI scan

 

Etiology:

o       Lipoma or interhemispheric cysts (preventing the progression of callosal axons as they are median structures) (7).

o       Late remodelling abnormality of callosal connections causing thinning of the corpus callosum may occur in utero or even at birth after severe asphyxia.

o       Prenatal ultrasound examination can usually diagnose CACC from 22 weeks onwards (8).

o       Absence of the cavum septi pellucidi, upward displacement and enlargement of the third ventricle

o       Enlarged occipital horns (colpocephaly) of the lateral ventricles,

o       separated and enlarged anterior horns,

o       enlarged interhemispheric spaces are the key indirect signs of CACC.

o         Color Doppler can also show the loss of the semicircular loop of the pericallosal artery (8)

 

 

 

PARTIAL AGENESIS (DYSGENESIS) OF THE CORPUS CALLOSUM

 

The caudal portion of the corpus callosum (splenium and body) are missing to various degrees.

Partial agenesis affects only the posterior part of the corpus callosum.

o       Indirect signs are lacking and prenatal diagnosis is therefore more difficult (9).

o       Hypoplasia occurs as a result of late destruction of the corpus callosum (10) owing to a metabolic, infectious or ischemic origin.

 

Amino acid metabolism
disorders

non-ketotic hyperglycinemia

maternal phenylketonuria

methyl malonic acidemia

Mitochondrial
disorders

pyruvate dehydrogenase deficiency

pyruvate decarboxylase deficiency

fumarase deficiency

Peroxisomal
disorders

Zellweger syndrome

Refsum syndrome

adrenoleukodystrophy

Other metabolic
disorders

glutaric acidemia

congenital disorder of glycosylation

3-hydroxyisobutyric aciduria

Ante or postnatal ischemic
or infectious events

necrotizing enterocolitis

severe birth asphyxia

antenatal cerebral vascular infarction

fetal toxoplasmosis or rubella

Chromosomal
abnormalities

trisomy 8, 13, 18, 21

Other syndromes

Menkes syndrome

Smith-Lemli-Opitz syndrome

Shapiro syndrome

fetal alcohol syndrome

acrocallosal syndrome

septo-optic dysplasia

ectodermal dysplasia

Other cerebral
abnormalities

defect of gyration pattern, microgyria

microcephaly

anomaly of cerebral white matter

cerebellar dysplasia

interhemispheric cyst

Paupe A, Bidat L, Sonigo P et.al. Prenatal diagnosis of hypoplasia of the corpus callosum in association with non-ketotic hyperglycemia.      Ultrasound Obstet Gynecol 2002;20:616-619


 

 

REFERENCES

  1. Pilu G, Sandri F, Perola A et.al. Sonography of fetal agenesis of the corpus callosum: A survey of 35 cases. Ultrasound Obstet Gynecol 1993;3:318.
  2. Gebarski SS, Gebarski KS, Bowerman RA et.al. Agenesis of the corpus callosum. Sonographic features. Radiology 1984;151:443.
  3. Babcock DS. The normal, absent and abnormal corpus callosum. Radiology 1984;151:449.
  4. Vergani P, Ghidini A, Mariani S et.al. Antenatal sonographic findings of agenesis of the corpus callosum. Am J Perinatol 1988;8:105.
  5. Lockwood CJ, Ghidini A, Aggarwal R et.al. Antenatal diagnosis of partial agenesis of the corpus callosum. A benign cause of ventriculomegaly. Am J Obstet Gynecol 1988;159:184.
  6. Hilpert PL, Kurtz AB. Prenatal diagnosis of agenesis of the corpus callosum using endovaginal ultrasound. J Ultrasound Med 1990;9:363.
  7. Wrainwright H, Bowen R, Radcliffe M. Lipoma of corpus callosum associated with dysraphic lesions and trisomy 13. Am J Med Genet 1995; 57: 10-3
  8. D'Ercole C, Girard N, Cravello L, Boubli L, Potier A, Raybaud C, Blanc B. Prenatal diagnosis of fetal corpus callosum agenesis by ultrasonography and magnetic resonance imaging. Prenat Diagn 1998; 18: 247-53
  9. Tepper R, Zalel Y, Gaon E, Fejgin M, Beyth Y. Antenatal ultrasonographic findings differentiating complete from partial agenesis of the corpus callosum. Am J Obstet Gynecol 1996; 174: 877-8
  10. Schaeffer GB, Bodensteiner JB, Thompson JN, Wilson DA. Clinical and morphometric analysis of the hypoplastic corpus callosum. Arch Neurol 1991; 48: 933-6
  11. Malinger G, Zakut H. The corpus callosum: normal fetal development as shown by transvaginal sonography. AJR Am J Roentgenol 1993; 161: 1041-3