Your browser doesn't support javascript.
loading
Relative prevalence and outcome of fetal posterior fossa abnormality.
Garg, Nikita; Kumar, Manisha; Rai, Preeti; Srivastava, Shivangi Shanker; Gupta, Amit; Roy Chaudhary, Subhasis.
Affiliation
  • Garg N; Department of Paediatrics, Southern Illinois University, Carbondale, Illinois, USA.
  • Kumar M; Fetal Medicine Subdivision, Department of Obstetrics and Gynecology, LHMC, New Delhi, India.
  • Rai P; Department of Pathology, LHMC, New Delhi, India.
  • Srivastava SS; Department of Obstetrics and Gynecology, LHMC, New Delhi, India.
  • Gupta A; Department of Pediatric surgery, AIIMS, Bhopal, India.
  • Roy Chaudhary S; Pediatric Surgery, KSCH, New Delhi, India.
J Paediatr Child Health ; 59(1): 107-115, 2023 01.
Article in En | MEDLINE | ID: mdl-36318816
ABSTRACT

AIM:

To find out the relative incidence and outcome of posterior fossa abnormality (PFA) in terms of survival at birth until 2 years of age.

METHODS:

We conducted a prospective study; all fetuses diagnosed with posterior fossa abnormality were followed-up. The outcome was observed with respect to survival, the presence of associated anomalies, the existence of developmental delay after a telephonic interview.

RESULTS:

Out of 2703 children with congenital anomalies, 921 (34.1%) had a central nervous system defect; 76 cases of PFA were fully followed. Dandy-Walker malformation (DWM) was present in 50% (38/76), mega cisterna magna 18.4% (14/76), Blake pouch cyst 13.2% (10/76), vermian hypoplasia (VH) 13.2% (10/76) and arachnoid cyst 5.2% (4/76). The diagnosis was possible before 20 weeks in only 12 (15.8%) cases. The mean gestational age at delivery was 34.7 ± 6.7 weeks. Associated anomalies were seen in 35/76 (46.1%) cases. A total of 35/76 (46.1%) survived after 2 years; there was developmental delay in 9.2% of cases.

CONCLUSION:

There is a large variation in the outcome of PFA depending upon the type of anomaly. Associated anomalies are common in VH and DWM, making their prognosis worse.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cysts / Dandy-Walker Syndrome Type of study: Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Child / Female / Humans / Infant / Newborn Language: En Journal: J Paediatr Child Health Journal subject: PEDIATRIA Year: 2023 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cysts / Dandy-Walker Syndrome Type of study: Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Child / Female / Humans / Infant / Newborn Language: En Journal: J Paediatr Child Health Journal subject: PEDIATRIA Year: 2023 Document type: Article Affiliation country: Estados Unidos