• World Neurosurg · Apr 2024

    Case Reports

    Keyhole Retrosigmoid Craniotomy for Lateral Pontine Cavernous Malformation.

    • Vsevolod Shurkhay, Brandon L King, Nikki J Acuff, Tyler S Auschwitz, and KalaniM Yashar SMYSDepartment of Neurological Surgery, St. John's Neuroscience Institute, Tulsa, Oklahoma, USA. Electronic address: yashar.kalani@ascension.org..
    • Department of Neurological Surgery, St. John's Neuroscience Institute, Tulsa, Oklahoma, USA.
    • World Neurosurg. 2024 Apr 1; 184: 4040.

    AbstractWith improvements in anesthesia, monitoring, and peroperative care, the surgical removal of intrinsic brainstem pathology has become a possibility.1 Although surgical removal of deep-seated lesions continues to have significant morbidity, at least temporarily, associated with it, removal of exophytic lesions can be accomplished with little disability for the patient. The key to a good outcome, when removing cerebral cavernous malformation, is preservation of adjacent neurovascular bundles, use of sharp dissection over blunt pulling, judicious use of cautery in and around the brainstem, and preservation of the developmental venous anomaly, when present. The authors present a case of a lateral pontine cerebral cavernous malformation that was exophytic at the lateral and peritrigeminal safe entry zones.2 Neuromonitoring was used an adjunct to ensure safety of the procedure. The lesion is accessed using a keyhole retrosigmoid craniotomy (Video 1). We do not routinely use lumbar drains for these procedures as careful arachnoid dissection can result in adequate cerebrospinal fluid release. The window of access to this area is between CN 5 and the CN 7/8 complex. The arachnoid over the nerves is preserved, but the layer between the nerves is exposed to gain access to the lateral pons. The lesion is sharply dissected from the lateral pons, taking care to save the developmental venous anomaly, from which this lesion arises.Copyright © 2024 Elsevier Inc. All rights reserved.

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