Presentation is loading. Please wait.

Presentation is loading. Please wait.

A RARE CASE OF EXENCEPHALY ABSTRACT ID- IRIA -1221.

Similar presentations


Presentation on theme: "A RARE CASE OF EXENCEPHALY ABSTRACT ID- IRIA -1221."— Presentation transcript:

1 A RARE CASE OF EXENCEPHALY ABSTRACT ID- IRIA -1221

2 20 years old G2 A1 lady Presented at 18 weeks POG for anamoly scan Antenatal period uneventful till date

3 U SG Obstetric USG Deficient cranial vault above the levels of orbit Brain tissue seen protruding out of the defect Polyhydramnios Provisional diagnosis - Exencepahaly

4 M RI Patient taken up for MRI same day To confirm presence of exencephaly T2 HASTE sequences were performed Fidings Supraorbital cranial vault was absent Disorganised brain tissue seen protruding out of the defect Bilaterally prominent orbits : Frog Eye sign

5 F INAL DIAGNOSIS EXENCEPHALY

6 D ISCUSSION ACRANIA- EXENCEPHALY- ANENCEPAHALY SEQUENCE Acrania is the absence of the calvarium; the skull base may be intact Exencephaly is acrania with protrusion of a substantial portion of the CNS into the amniotic cavity Anencephaly is acrania with absence of most or all of the brain tissue Anencephaly is classified anatomically as merocrania when the defect does not involve the foramen magnum holoacrania when the defect extends through the foramen magnum; Holoacrania with rachischisis if spinal defects are associatedType of Neural tube defect

7 DISCUSSION Incidence is around 1:1000. There is a recognised female predilection with a F:M of ~4:1. As with many other malformations, a number of associated abnormalities are recognised: other neural tube defects: spina bifida (especially cervical) congenital heart defects cleft lip/palate diaphragmatic hernia(s) spinal dysraphism skeletal anomalies: e.g. clubfeet gastrointestinal abnormalities: e.g. omphalocele urinary tract abnormalities: hydronephrosis most common

8 EXENCEPHALY Exencephaly is characterised by calvarial absence and loss of fetal brain tissue to variable degrees and is considered a precursor to anencephaly in the acrania-exencephaly-anencephaly sequence. Absence of the cranial vault exposes the brain to contact with the amniotic fluid. Initially, an excessive growth of the encephalic structures occurs with a normal development of eyes and cranial nerves Susequently, destructive processes of the exposed brain occur The eventual result is anencephaly Markers : maternal serum alpha feto protein (MSAFP) levels are highly elevated

9 R ADIOGRAPHIC FEATURES Imaging features have some overlap with that of anencephaly except that there is some brain tissue presence: cranial vault is absent or poorly formed, cephalad to orbits nasal bone may be absent in most cases brain tissue is herniating or dangling in amniotic fluid brain tissue may be attached to the amniotic membrane

10 US is an extremely accurate technique for the diagnosis of acrania, with almost 100% sensitivity. Transvaginal US can be useful when the fetal head is low in the pelvis and not easily visible The calcification of the bone structures of the skull can be discerned at the 10th week of gestation; therefore, it is suggested not to attempt a diagnosis before this week

11 The characteristic US feature is represented by absent visualization of the cranial vault above the orbits, which appear prominent; the thalami and ventricles are not detectable In anencephaly it is difficult to recognize the cerebral tissue, while in exencephaly it is usually possible to detect a normal amount of cerebral tissue

12 AMNIOTIC BAND SEQUENCE WITH EXENCEPHALY Amniotic bands are thin fibrous bands causing regional constrictions, amputations and disruption of cranial bone formation.The brain tissue is covered by only a vascular layer of epithelium, and can be slowly degraded by the amniotic fluid and degenerate into anencephaly. MRI : Usually HASTE T2 or SSFSE sequence is used, which is very fast and thus prevents motion artifacts

13 PROGNOSIS Exencephaly is a precursor to anencephaly, and essentially a lethal condition Advise and counselling for abortion is to be given to the parents.

14

15 REFRENCES 1. Wilkins-haug L, Freedman W. Progression of exencephaly to anencephaly in the human fetus--an ultrasound perspective. Prenat. Diagn. 1991;11 (4): Bianchi DW, Crombleholme TM, D'Alton ME. Fetology, diagnosis & management of the fetal patient. McGraw-Hill Professional. (2000) 3. Timor-tritsch IE, Greenebaum E, Monteagudo A et- al. Exencephaly-anencephaly sequence: proof by ultrasound imaging and amniotic fluid cytology. J Matern Fetal Med. 5 (4): Papp Z, Csécsei K, Tóth Z et-al. Exencephaly in human fetuses. Clin. Genet. 1986;30 (5): Merz E, Bahlmann F. Ultrasound in obstetrics and gynecology. Thieme Medical Publishers. (2005)


Download ppt "A RARE CASE OF EXENCEPHALY ABSTRACT ID- IRIA -1221."

Similar presentations


Ads by Google