Objective: The aim of the study was to identify concomitant hidden skull base defects in patients
with a persistent lateral craniopharyngeal canal (Stenberg canal CSF fistula). Study Design: Retrospective analysis. Methods: We reviewed patients who were operated for a Sternbergs canal CSF fistula from 2007
to 2014 at Ankara University. In addition to imaging, all patients received preoperative
intrathecal 5% sodium fluorescein. Endonasal endoscopic approach was used for repair,
nearby a bilateral diagnostic endoscopy with fluorescein filter, performed to search
for concomitant defects. Results: A total of five Sternberg canal CSF fistula patients were operated. Other than primary
defects at expected locations on sphenoid sinus lateral walls, we identified a second
hidden skull base defect as a small meningocele without CSF leakage in two patients.
Both defects were around olfactory fibers, one located at the contralateral anterior
and other at the ipsilateral posterior cribriform plate according to the side of primary
defects. In all patients, watertight closure of all CSF fistulas and all identified
skull base defects were achieved and no recurrences were observed in a mean follow-up
time of 32 months. Conclusion: In our caseload patients who were diagnosed for a Sternberg canal CSF fistula had
a second skull base defect with a high percentage. Surgeons should be aware of this
fact and repair these as well, to entirely protect patients from the risk of ascending
meningitis.