gms | German Medical Science

63. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC)
Joint Meeting mit der Japanischen Gesellschaft für Neurochirurgie (JNS)

Deutsche Gesellschaft für Neurochirurgie (DGNC) e. V.

13. - 16. Juni 2012, Leipzig

Anterior skull base surgery in pediatrics – Neurologic long-term outcome

Meeting Abstract

  • O. Bozinov - Klinik für Neurochirurgie, UniversitätsSpital Zürich, Schweiz
  • C. Unsinn - Klinik für Neurochirurgie, UniversitätsSpital Zürich, Schweiz
  • M. Neidert - Klinik für Neurochirurgie, UniversitätsSpital Zürich, Schweiz
  • J.K. Burkhardt - Klinik für Neurochirurgie, UniversitätsSpital Zürich, Schweiz
  • M. Grotzer - Klinik für Neuro-Onkologie, KinderSpital Zürich, Universität Zürich, Schweiz

Deutsche Gesellschaft für Neurochirurgie. Japanische Gesellschaft für Neurochirurgie. 63. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC), Joint Meeting mit der Japanischen Gesellschaft für Neurochirurgie (JNS). Leipzig, 13.-16.06.2012. Düsseldorf: German Medical Science GMS Publishing House; 2012. DocSA.02.08

doi: 10.3205/12dgnc318, urn:nbn:de:0183-12dgnc3188

Veröffentlicht: 4. Juni 2012

© 2012 Bozinov et al.
Dieser Artikel ist ein Open Access-Artikel und steht unter den Creative Commons Lizenzbedingungen ( Er darf vervielfältigt, verbreitet und öffentlich zugänglich gemacht werden, vorausgesetzt dass Autor und Quelle genannt werden.



Objective: Anterior skull base tumors are rare in the pediatric population. Surgical removal may result in long-term complications, especially due to the delicate anatomic structures in this particular location. This study aims to evaluate perioperative complications and clinical outcome over a long time period.

Methods: 61 patients diagnosed with anterior skull base tumors (30 girls and 31 boys) under 18 years of age (mean 9.95, SD 4.84, range 0.08–7.8 years) were treated at our institution from 2000 to 2010. Medical records were analyzed retrospectively for epidemiological data, histology, treatment modality including surgical approach, perioperative complications, as well as short- and long-term clinical outcome. Postoperative histologic diagnoses included 20 craniopharyngiomas, 14 pilocytic astrocytomas, 8 pituitary adenomas and 19 rare tumor entities. Surgical approaches included 43 frontal craniotomies and 15 transsphenoidal approaches.

Results: Of 61 patients 58 are still alive (OS 95%) – three patients died between the ages of 6 months and 8 years, all due to progression of malignant rhabdoid tumors. Postoperative neurological complications included transient postoperative seizures (11, 18,3%), transient hemiparesis (4, 6.7%), permanent seizures (4, 6,7%), persistent hemiparesis (2, 3.4%), and 18 patients with cranial nerve lesions (6 transient 10% and 12 persistent 20%). CSF leaks were seen and treated in 10 patients (16.4%). 35 patients had no visual changes (58.3 %). Improvement of visual acuity was seen in 6 patients (10%) and reduction of vision in 15 children (25%). Total loss of vision in one eye was seen in 4 cases (6.7%). New onset obesity (weight >97. percentile) was highly associated with craniopharyngiomas (8, 40%) compared to other histologies (P=0.023). Other statistically significant associations were observed: Strabismus divergens and pilocytic astrocytoma (P=0.002), scotomas and craniopharyngiomas (P=0.045), postoperative short-term epilepsy in frontal craniotomies compared to transsphenoidal approaches (P=0.037), deterioration in school performance was associated with multiple surgeries (P=0.012) and all post-operative cases of pubertas praecox had a new onset of obesity (P=0.037).

Conclusions: Overall survival after anterior skull base surgery in the pediatric population is favorable, if the diagnosis is not malignant rhabdoid tumor. However, surgically aggressive treatment is associated with various significant neurological, visual and endocrinological long-term effects.