Introduction
The parietal lobe is often considered a safe entry point for cortical and subcortical tumors because it avoids the somatosensory cortex anteriorly and the visual cortex posteriorly. However, there are a variety of parietal lobe symptoms that can develop from accessing lesions in this region, which include Gerstmann syndrome (right-left confusion, agraphia, and acalculia), aphasia, and agnosia in the dominant hemisphere, as well as constructional apraxia, dressing apraxia, and anosognosia in the nondominant hemisphere. In a study on parietal lobe gliomas, 34 of 119 (29%) parietal gliomas were low-grade gliomas (LGGs). The most common deficits following parietal glioma surgery were dysphagia, sensory deficits, vision changes, and parietal lobe syndromes that occurred in 26% of patients. In this chapter, we present a case of a nondominant-hemisphere, parieto-occipital, LGG.
Chief complaint: headaches
History of present illness
A 46-year-old, right-handed woman with hypertension presented with headaches. She has had intermittent episodes of excruciating headaches without nausea or vomiting that were different from her typical headaches. She was seen by her primary care physician who ordered imaging, which revealed a brain lesion ( Fig. 9.1 ). She was referred for evaluation and management.
Medications : Lisinopril.
Allergies : No known drug allergies.
Past medical and surgical history : Hypertension.
Family history : No history of intracranial malignancies.
Social history: Cashier. No smoking, occasional alcohol.
Physical examination : Awake, alert, oriented to person, place, and time; Language: intact naming and repetition; Cranial nerves II to XII intact; No drift, moves all extremities with full strength.

Hugues Duffau, MD, PhD, University Hospital of Montpellier, Montpellier, France | Shawn L. Hervey-Jumper, MD, University of California at San Francisco, San Francisco, CA, United States | Randy L. Jensen, MD, PhD, University of Utah, Salt Lake City, UT, United States | Stephen J. Price, MBBS, PhD, University of Cambridge, Cambridge, United Kingdom | |
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Preoperative | ||||
Additional tests requested | Neuropsychological assessment Repeat MRI for growth rate fMRI+DTI (research) | DTI MEG Neuropsychological assessment | Ophthalmology (visual field testing) | Ophthalmology (visual field testing) MRI perfusion with rCBV Steroid trial |
Surgical approach selected | Right parietal awake craniotomy with cortical and subcortical mapping of precuneus, posterior cingulate, and splenium | Right parieto-occipital craniotomy with cortical and subcortical mapping | Right occipital craniotomy with interhemispheric | Right occipital craniotomy with 5-ALA if no response to steroids and rCBV greater than 3 |
Anatomic corridor | Right superior parietal lobule | Right parieto-occipital cortex | Right occipital interhemispheric | Right occipital interhemispheric |
Goal of surgery | Extensive resection (GTR or NTR) with preservation of neurologic and cognitive functions | GTR with patient agreeing to accepting hemianopsia | GTR with expected visual field deficits | Resection of tumor with likely hemianopia |
Perioperative | ||||
Positioning | Lateral | Prone | Prone | Prone |
Surgical equipment | Brain stimulator Dedicated team (anesthesia, neuropsychological, speech pathology) No neuronavigation, intraoperative MRI, microscope, or functional neuroimaging | Surgical navigation Surgical microscopeBipolar and monopolar brain stimulator Ultrasonic aspirator | Surgical navigation MEPs Ultrasonic aspirator Intraoperative MRI | Surgical navigation Surgical microscope with 5-ALA Ultrasound Ultrasonic aspirator Budde halo retractor |
Medications | Steroids Antiepileptics | Antiepileptics Steroids Mannitol | Steroids | 5-ALA Mannitol Steroids |
Anatomic considerations | Postcentral sulcus anteriorly, intraparietal sulcus laterally, parieto-occipital sulcus posteriorly; somatosensory thalamocortical pathway anteriorly, SLF II laterally, optic tracts, cingulate | Superior sagittal sinus, callosomarginal and pericallosal arteries, cingulate gyrus | Visual cortex, visual fields | Venous sinuses and draining veins |
Complications feared with approach chosen | Sensorimotor deficit, movement control, visual fields, spatial cognition, executive function, mentalizing, conscious awareness | Visual field defects, stroke | Visual field deficit | Hemianopia, central visual defect |
Intraoperative | ||||
Anesthesia | Asleep-awake-asleep | General | General | General |
Skin incision | Arciform mark | U-shaped | Linear | Linear paramedian |
Bone opening | Right parietal | Right occipital | Right parietal | Right occipital |
Brain exposure | Right central and parietal | Right occipital | Right parietal | Right occipital |
Method of resection | Opening under general anesthesia with laryngeal mask airway, bone flap exposing parietal lobe and perirolandic area, patient awoken prior to dural opening after dural anesthesia, cortical mapping at low intensity (1.5–3 mA) with counting/left upper and lower extremities/line bisection task/monitoring visual fields/conscious awareness, subpial dissection concurrent with mapping and functional testing, resection up to functional boundaries of somatosensory tracts/SLF/cingulate/optic tracts, general anesthesia for closure | Right parieto-occipital craniotomy ipsilateral to sagittal sinus, cortical bipolar motor mapping to identify somatosensory cortex, transparietal approach, focus on anterior and medial margins first, subpial dissection down to U-fibers, expose falx/cingulate sulcus/callosomarginal arteries, subcortical monopolar mapping along anterior and lateral margins finish with cingulate resection working medially within cingulate gyrus until corpus callosum is identifiedcortical bipolar motor mapping to identify somatosensory cortex, transparietal approach focus on anterior and medial margins first, subpial dissection down to U fibers, expose falx/cingulate sulcus/callosomarginal arteries, subcortical monopolar mapping along anterior and lateral margins, finish with cingulate resection working medially within cingulate gyrus until corpus callosum is identified. | Right occipital craniotomy, interhemispheric approach, subpial dissection, identify tumor and corticectomy and debulk tumor, continuous MEP monitoring, intraoperative MRI for potential further resection | Right occipital craniotomy with burr holes on midline and spanning contralateral side above transverse sinus, cruciate dural opening and monitor for draining veins, mobilize occipital lobe, CSF drainage, retraction away from visual cortex, mobilize along falx to free end and visualize corpus callosum, blue light with fluorescence (unlikely), ultrasound to visualize best trajectory, continue corticectomy of posterior margin avoiding primary visual cortex, debulk tumor on deeper margin on medial side, rotate right side to get better view of lateral surface and debulk laterally, posterolateral corner may be difficult to visualize, watertight dural closure |
Complication avoidance | Cortical and subcortical mapping with counting, left upper and lower extremity movement, line bisection, visual field monitoring, conscious awareness | Subpial resection, cortical and subcortical mapping, cingulate portion last | Interhemispheric approach, continuous MEP recording, intraoperative MRI for further resection | Craniotomy spans to contralateral side, monitor for bridging veins, avoid primary visual cortex, debulk medial side first |
Postoperative | ||||
Admission | ICU | Intermediate care | ICU | Floor |
Postoperative complications feared | Movement, executive functions, spatial cognition, visual field, high-level mentalizing | Stroke, visual field defect (expected) | Visual field deficit | Visual field deficit |
Follow-up testing | MRI within 24 hours after surgery Neuropsychological testing 2 days after surgery | MRI within 48 hours after surgeryNeuropsychological testing at 1 and 3 months after surgeryCognitive rehab as needed | MRI within 48 hours after surgery Visual field testing 3 months | MRI within 72 hours after surgery Visual field testing 1 month after surgery |
Follow-up visits | Cognitive rehabilitation, MRI 3 months and then every 3–6 months throughout lifetime | 14 days after surgery, 1 and 3 months neuropsychological assessments | 4–6 weeks after surgery | 7 days after surgery |
Adjuvant therapies recommended | ||||
Diffuse astrocytoma (IDH mutant, retain 1p19q) | STR–observation for growth rate GTR–observation for growth rate | STR–radiation/temozolomide GTR–observation | STR–radiation/temozolomide GTR–radiation/temozolomide | STR–radiation/temozolomide GTR–observation |
Oligodendroglioma (IDH mutant, 1p19q LOH) | STR–growth rate observation GTR–growth rate observation | STR–tumor board discussion, likely chemoradiation GTR–observation | STR–radiation/temozolomide GTR–observation | STR–radiation/PCV GTR–observation |
Anaplastic astrocytoma (IDH wild type) | Homogenous AA-temozolomide AA foci removal with GTR of FLAIR abnormality–treatment as for diffuse astrocytoma | STR–radiation/temozolomide GTR–radiation/temozolomide | STR–radiation/temozolomide GTR–radiation/temozolomide | STR–radiation/temozolomide GTR–radiation/temozolomide |

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