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DOI 10.1111/jpc.16254

Медицинская библиотека · Journal of paediatrics and child health · 2022

Relative prevalence and outcome of fetal posterior fossa abnormality.

Garg Nikita, Kumar Manisha, Rai Preeti, Srivastava Shivangi Shanker, Gupta Amit, Roy Chaudhary Subhasis

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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.

Для цитирования: Garg Nikita, Kumar Manisha, Rai Preeti, Srivastava Shivangi Shanker, Gupta Amit, Roy Chaudhary Subhasis. Relative prevalence and outcome of fetal posterior fossa abnormality.. Journal of paediatrics and child health. 2022. DOI: 10.1111/jpc.16254.

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