Introduction
The surgery of brain tumors, namely gliomas, requires a delicate balance between extensive resection and avoidance of neurologic deficits. The risk of neurologic deficits is highest in those tumors that involve eloquent motor and/or language cortical and subcortical regions. There are a variety of methods for monitoring these pathways, which include passive monitoring, including motor evoked potentials (MEP) and somatosensory evoked potentials (SSEP), as well as direct monitoring, including cortical stimulation. These methods are most utilized for lesions involving motor pathways. In this chapter, we present a high-grade glioma that is in close proximity and possibly involves the perirolandic region and corticospinal tracts in the nondominant hemisphere.
Chief complaint: left-sided weakness
History of present illness
A 41-year-old, right-handed man with no significant past medical history presented with progressive left-sided weakness. Over the past 3 weeks, he developed progressive left arm and leg weakness to the point in which he could not button his shirt and was dragging his leg while he was walking. He was seen by his primary care physician who ordered brain imaging that revealed a brain lesion ( Fig. 17.1 ). He was referred for evaluation and management.
Medications : None.
Allergies : No known drug allergies.
Past medical and surgical history : None.
Family history : Father died of glioblastoma within the last couple of months.
Social history : Works as an engineer. No smoking history or alcohol.
Physical examination : Awake, alert, oriented to person, place, and time; Cranial nerves II to XII intact; Left drift, left upper extremity 4/5, left lower extremity 4+/5, right upper extremity/right lower extremity 5/5.
Imaging : Chest/abdomen/pelvis computed tomography negative for primary malignancy.

Mark Bernstein, MD, University of Toronto, Toronto, Canada | Chetan Bettegowda, MD, PhD, Johns Hopkins University, Baltimore, MD, United States | Randy L. Jensen, MD, PhD, University of Utah, Salt Lake City, UT, United States | Eslam Mohsen Mahmoud Hussein, MBBS, MSc, Ain Shams University, Cairo, Egypt | |
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Preoperative | ||||
Additional tests requested | DTI fMRI | DTI | DTI | DTI fMRI Neuropsychological assessment |
Surgical approach selected | Right frontal awake craniotomy for tumor for motor and sensory mapping | Right frontal craniotomy with tubular retractor and asleep motor mapping | Right frontal-parietal craniotomy for tumor with asleep cortical mapping and intraoperative MRI | Right posterior frontal or parieto-occipital craniotomy |
Anatomic corridor | Right frontal | Right frontal lateral and anterior to motor cortex | Right frontal | Right posterior frontal |
Goal of surgery | Maximal safe resection of enhancing portion of the tumor | Gross total resection of enhancing component | Gross total resection of enhancing component | Gross total resection of enhancing component |
Perioperative | ||||
Positioning | Right supine with left rotation | Right supine | Right supine 30-degree rotation | Right supine with left rotation |
Surgical equipment | Surgical navigation Surgical microscope Brain stimulator | Surgical navigation IOM (MEP, SSEP, EEG) Brain stimulator Surgical microscope Tubular retractors | Surgical navigation Ultrasonic aspirator Brain stimulator IOM (SSEP/MEP/phase reversal) Intraoperative MRI | Surgical navigation Ultrasonic aspirator Surgical microscope |
Medications | Steroids | Steroids Antiepileptics Mannitol | Steroids | Steroids Antiepileptics Mannitol Diuretics |
Anatomic considerations | Precentral gyrus | Precentral gyrus, SMA, internal capsule | Central sulcus, precentral gyrus | Precentral gyrus |
Complications feared with approach chosen | Motor deficit | Motor deficit | Motor deficit | Motor deficit |
Intraoperative | ||||
Anesthesia | Asleep | General | General | General |
Skin incision | Linear | Linear | Linear/curvilinear | Linear |
Bone opening | Right frontal | Right frontal | Right frontal-parietal | Right posterior frontal or parieto-occipital |
Brain exposure | Right frontal | Right frontal | Right frontal-parietal | Right posterior frontal or parieto-occipital |
Method of resection | Regional field block with local anesthetic, craniotomy based on navigation over lesion, cruciate dural opening, motor and speech mapping with electrocortical stimulation, find pseudoplane between tumor and normal parenchyma, stay 1 cm away from positive mapping sites, periodic confirmation with navigation, close when satisfied with maximal resection | Craniotomy to encompass lesion based on navigation, cruciate dural opening, placement of strip electrode and phase reversal to identify motor cortex, stimulate cortex to confirm absence of motor cortex, small corticectomy over negative motor mapping site, place tubular retractor into hematoma, debulk hematoma to reduce mass effect, debulk remaining tumor with continuous subcortical mapping | Craniotomy based on navigation, dural opening, placement of strip electrode, and phase reversal assessment, identify tumor volume based on navigation, cortical mapping to confirm absence of motor cortex, corticectomy over negative mapping sites, microscopic guided resection with continuous MEP, subcortical mapping as needed for deep portion of tumor, intraoperative MRI when maximal resection anticipated, further resection with recalibrated navigation if necessary | Larger craniotomy to avoid postoperative edema, monitor for increased intracranial pressure based on dural pulsation, cruciate dural opening if not tense, trajectory based on DTI and navigation, small corticectomy over nonfunctional areas, attempt to find a cleavage plane, debulk tumor without violating neural structures, expansile duraplasty if brain swelling, closure with subgaleal drain |
Complication avoidance | Awake motor and speech mapping, staying 1 cm away from positive mapping sites | IOM, cortical and subcortical mapping | IOM, cortical and subcortical mapping, intraoperative MRI | DTI, finding cleavage plane around tumor |
Postoperative | ||||
Admission | Outpatient | ICU | ICU | ICU |
Postop complications feared | Motor deficit | Seizures, motor deficit, hydrocephalus, intraventricular hemorrhage | Motor deficit | Motor deficit, seizure, altered mental status |
Follow-up testing | CT within 4 hours after surgery MRI prior to radiation | CT immediately after surgery MRI within 24 hours after surgery Physical and occupational therapy | MRI within 48 hours after surgery | CT with and without contrast within 48 hours after surgery MRI before radiation therapy |
Follow-up visits | 10–14 days after surgery and follow-up with radiation and neurooncology | 14 days after surgery | 2–4 weeks with neurooncology 4–6 weeks after surgery | 10 days after surgery |
Adjuvant therapies recommended | ||||
IDH status | Mutant–radiation/temozolomide Wild type–radiation/temozolomide | Mutant–radiation/temozolomide Wild type–radiation/temozolomide | Mutant–radiation/temozolomide Wild type–radiation/temozolomide | Mutant–whole brain radiation/temozolomide or bevacizumab Wild type–whole brain radiation therapy, neurooncology evaluation |
MGMT status | Methylated–radiation/temozolomide Unmethylated–radiation/ temozolomide | Methylated–radiation/temozolomide Unmethylated–radiation/temozolomide | Methylated–radiation/temozolomide Unmethylated–radiation/temozolomide | Methylated–whole brain radiation/temozolomide or bevacizumab Unmethylated–whole brain radiation therapy, neurooncology evaluation |

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