Introduction
Historically, the Wernicke area has been defined as residing primarily within the posterior superior temporal lobe in the dominant hemisphere. , However, there is great individual variability. , The methods of identifying this area radiographically primarily involve functional magnetic resonance imaging (MRI), in which neurovascular coupling allows the identification of flow changes in conjunction with neuronal activity. The difficulty with functional MRI is that it is prone to false positives and false negatives, does not identify critical functional thresholds, and can be less sensitive and/or specific in tumor-infiltrated and/or edematous areas that are common for gliomas, especially high-grade gliomas. The direct method of identifying these areas is awake brain mapping with direct electrical stimulation, whereby electrical stimulation impairs normal neurologic firing to identify functional processes. In this chapter, we present a case of a high-grade glioma in close proximity to the superior temporal gyrus, which has historically been identified as the Wernicke area.
Chief complaint: speaking difficulties
History of present illness
A 51-year-old, right-handed man with a history of hypertension presented with difficulty speaking. Over the past 2 months, he has noticed an increased difficulty getting the right words out, especially during business meetings. He has also had several instances in which his words did not sound right. He underwent brain imaging that revealed a brain lesion ( Fig. 20.1 ).
Medications : Hydrochlorothiazide.
Allergies : No known drug allergies.
Past medical and surgical history : Hypertension.
Family history : No history of intracranial malignancies.
Social history: Business executive, no smoking or alcohol history.
Physical examination : Awake, alert, oriented to person, place, and time; Language: slowness in speech, dysarthria, intact naming and repetition; Cranial nerves II to XII intact; No drift, moves all extremities with full strength.
Imaging : Chest/abdomen/pelvis imaging negative for primary malignancy.
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Mitchel S. Berger, MD, University of California at San Francisco, San Francisco, CA, United States | Shawn L. Hervey-Jumper, MD, University of California at San Francisco, San Francisco, CA, United States | Manabu Natsumeda, MD, PhD, Niigata University, Niigata, Japan | Pierre A. Robe, MD, PhD, University Medical Center of Utrecht, The Netherlands | |
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Preoperative | ||||
Additional tests requested | DTI MEG | DTI MEG Neuropsychological assessment | fMRI DTI Neuropsychological assessment Angiography and Wada test 3D-CTA/CTV | Neuropsychological assessment |
Surgical approach selected | Left temporal-parietal craniotomy with awake language and motor cortical and subcortical mapping with 5-ALA | Left temporal craniotomy with awake language mapping with 5-ALA | Left parietal awake craniotomy with cortical and subcortical mapping | Left temporo-parietal awake craniotomy with cortical and subcortical mapping with 5-ALA |
Anatomic corridor | Left temporal-parietal with awake cortical and subcortical mapping | Left STG | Left parietal | Left posterior temporal |
Goal of surgery | Complete resection of the enhancing and as much FLAIR as possible | Maximal resection of enhancing core and FLAIR with minimal language morbidity | Complete resection of the enhancing and as much FLAIR as possible | Maximal resection of FLAIR according to functional boundaries |
Perioperative | ||||
Positioning | Left supine | Left semilateral | Right lateral (left side up) | Left park bench |
Surgical equipment | Surgical navigation Surgical microscope with 5-ALA Brain stimulator | Surgical navigation IOM (ECoG) Surgical microscope with 5-ALA Brain stimulator Ultrasonic aspirator | Surgical navigation IOM (MEP/SSEP) Brain stimulator Surgical microscope with 5-ALA Intraoperative CT | Surgical navigation Ultrasound Neuropsychological testing Surgical microscope |
Medications | Mannitol Steroids Antiepileptics | Mannitol Steroids Antiepileptics | Mannitol Steroids Antiepileptics | Steroids Mannitol |
Anatomic considerations | Language cortical and subcortical areas | STG, MTG, SLF, AF, IFOF, uncinate, ILF, MdLF | Angular artery, temporal occipital artery, SMG, AG, STG, AF, IFOF, MdLF, Sylvian fissure, vein of Labbe | Temporal cortex, optic radiations, IFOF |
Complications feared with approach chosen | Language deficits | Long-term language deficits | Language dysfunction, Gerstmann syndrome, visual field deficit | Speech deficit, prosopagnosia, working memory deficit, quadrantopsia |
Intraoperative | ||||
Anesthesia | Asleep-awake-asleep | Asleep-awake-asleep | Asleep-awake-asleep | Awake |
Skin incision | Inverted U | Inverted U | Horseshoe | Semicircular, supraauricular |
Bone opening | Left temporal-parietal with 2-cm margin | Left temporal | Left temporal-parietal | Left temporal-parietal |
Brain exposure | Left temporal-parietal | Left temporal | Left temporal-parietal | Left temporal-parietal |
Method of resection | Skin anesthetized, craniotomy overlying lesion with 2-cm margin based on navigation, dural opening, awake language cortical mapping, corticectomy based on negative mapping areas, continue resection with continuous subcortical language mapping, aim to resect all enhancement as well as FLAIR pending mapping results, resection until positive cortical and subcortical mapping, 5-ALA fluorescence assessemnts for residual, watertight dural closure, subgaleal drain insertion | Local anesthetic into pins sites, wide scalp block, myocutaneous flap extended inferiorly, confirm body temperature and optimal mapping conditions, mapping team present including neurology and speech pathology, language mapping over STG and MTG to determine positive mapping threshold, mapping over tumor site with 1-cm margin around FLAIR, entry into functional free zones with ultrasonic aspirator, resection first along anterior and medial FLAIR margins subpially and then lateral margin down to subcortical U-fibers, mass truncated at bottom of sulcus, subcortical stimulation until medial margin reached | Scalp bloc, LMA, craniotomy based on navigation, awaken patient and removal of LMA, language mapping, corticectomy based on negative mapping results, resection of enhancing portion with ultrasonic aspirator and suction, check for 5-ALA staining, removal of FLAIR portion until positive mapping areas reached, patient put back to sleep with LMA, continuous monitoring, intraoperative CT to guide further resection, watertight dural closure, insertion of subgaleal drain | Local field block, myocutaneous opening, left temporal/pterional bone flap, ultrasound to delineate tumor margins, opening dura, ECoG, cortical stimulation for positive sites (1–3 mA), tumor resection with repetitive cortical and subcortical stimulation, decrease simulation to 2 and 1 mA near eloquent area, ultrasound to evaluate extent of resection and hematoma |
Complication avoidance | Language mapping, continuous monitoring | Language mapping, subcortical mapping once sulcus level reached | Language mapping, continuous monitoring, intraoperative CT | Cortical and subcortical stimulation, ultrasound |
Postoperative | ||||
Admission | ICU | ICU | ICU | Floor |
Postoperative complications feared | Language dysfunction, seizures | Language dysfunction, venous infarct | Language dysfunction, Gerstmann syndrome, visual field deficit | Language dysfunction, vasospasm, seizure |
Follow-up testing | MRI within 24 hours after surgery with DWI and DTI | MRI within 48 hours after surgery Speech evaluation 24 hours after surgery | CT immediate postoperative MRI within 24 hours after surgery Neuropsychological assessment 7 days after surgery | MRI within 72 hours after surgery Postoperative neuropsychological assessment and 3 months after surgery |
Follow-up visits | 10 days after surgery with neurooncology | 14 days after surgery | On pathology diagnosis | As needed with neurosurgery Speech therapy |
Adjuvant therapies recommended | ||||
IDH status | Mutant–radiation/temozolomide +/– lomustine Wild type–radiation/temozolomide +/– lomustine | Mutant–radiation/temozolomide Wild type–radiation/temozolomide | Mutant–radiation/temozolomide with TTF Wild type–radiation/temozolomide with TTF | Mutant–radiation/temozolomide Wild type–radiation/temozolomide |
MGMT status | Methylated–radiation/temozolomide Unmethylated–radiation/temozolomide under 65 years of age | Methylated–radiation/temozolomide Unmethylated–radiation/temozolomide | Methylated–radiation/temozolomide +/– TTF Unmethylated–radiation/temozolomide +/– TTF | Methylated–radiation/temozolomide Unmethylated–radiation/temozolomide |
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