From: Risk and prognostic factors in patients with congenital encephalocele
Sex | |
Male | 14 (46.67%) |
Female | 16 (53.33%) |
Location | |
Occipital | 20 (66.7%) |
Occipitocervical | 6 (20%) |
Parietal | 2 (6.7%) |
Basal (transehmoidal) | 1 (3.3%) |
Frontoethmoidal | 1 (3.3%) |
Size | (9.10 × 9.38) ± (8.18 × 8.04) |
Content | |
Neural tissue | 19 (63.33%) |
Head circumference | |
< 35 cm | 7 (23.33%) |
≥ 35 cm | 23 (76.66%) |
Sac rupture with CSF leak | 2 (6.67%) |
Cranial anomalies | |
Corpus callosum dysgenesis | 6 (20.0%) |
Dandy–Walker malformation | 2 (6.67%) |
Preoperative hydrocephalous | 2 (6.67%) |
Microcephaly | 7 (23.33%) |
Total | 17 (56.66%) |
Extracranial anomalies | |
Cleft lip | 2 (6.67%) |
Klippel feil syndrome | 2 (6.67%) |
Microtia | 1 (3.33%) |
Polycystic kidney | 1 (3.33%) |
Cardiac anomalies | 2(6.67) |
Complication | |
Wound infection | 2 (6.67%) |
CSF leaking from repaired wound | 3 (10.0%) |
Postoperative hydrocephalus | 5 (16.67%) |
Seizures | 6 (20%) |
Outcome | |
Good | 13 (43.3%) |
Delayed development | 14 (46.7%) |
Died | 3 (10.0%) |