Introduction
Historically, the Broca area has been defined as residing primarily within the pars triangularis of the inferior frontal gyrus or frontal operculum on the dominant hemisphere. , The methods of identifying this area radiographically primarily involves functional magnetic resonance imaging (fMRI), in which neurovascular coupling allows the identification of flow changes in conjunction with neuronal activity. The difficulty with fMRI is that it is prone to false positives and false negatives, does not identify critical threshold of functions, and can be less sensitive and/or specific in tumor-infiltrated and/or edematous areas that is common for 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 inferior frontal gyrus, which has historically been identified as the Broca area.
Chief complaint: speaking problems and confusion
History of present illness
A 59-year-old, right-handed woman with a history of hypertension, hyperlipidemia, and anxiety presented with confusion and speaking problems. Her family states that over the past couple of months they have noted that she has become increasingly confused and with difficulty getting her words out. She was seen by a neurologist who ordered imaging that showed a large brain lesion ( Fig. 19.1 ).
Medications : Lisinopril, atorvastatin, sertraline.
Allergies : No known drug allergies.
Past medical and surgical history : Hypertension, hyperlipidemia, anxiety.
Family history : No history of intracranial malignancies.
Social history: Homemaker, 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; Right drift, moves all extremities with full strength.
Imaging : Chest/abdomen/pelvis imaging negative for primary malignancy.

Jeffrey N. Bruce, MD, Columbia University, New York City, NY, United States | Chae-Yong Kim, MD, PhD, Seoul National University, Bundang Hospital, Seoul, South Korea | Ganesh Rao, MD, Baylor College of Medicine, Houston, TX, United States | Jinsong Wu, MD, PhD, Fudan University, Huashan Hospital, Shanghai, China | |
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Preoperative | ||||
Additional tests requested | DTI fMRI Neuropsychological assessment | DTI Perfusion and diffusion MRI +/– fMRI PET | fMRI Neuropsychological assessment | DTI Task-based BOLD fMRI MRS Neuropsychological assessment |
Surgical approach selected | Left frontal craniotomy with awake language and motor mapping | Left frontal craniotomy with 5-ALA | Left frontal craniotomy | Left frontal craniotomy with awake language and motor mapping with intraoperative MRI |
Anatomic corridor | Left frontal over tumor | Left frontal | Left frontal above frontal sinus | Left frontal |
Goal of surgery | Extensive resection of contrast and FLAIR with functional preservation | Attempted gross total resection | Diagnosis because of insula involvement and maximal safe resection | Maximal safe resection of enhancing component |
Perioperative | ||||
Positioning | Left supine with slight right rotation | Left supine with 5-degree right rotation | Left supine | Left supine with 30-degree right rotation |
Surgical equipment | Surgical navigation IOM (ECoG) Brain stimulator Ultrasound Ultrasonic aspirator Surgical microscope | Surgical navigation IOM Ultrasound Surgical microscope with 5-ALA Ultrasonic aspirator | Surgical navigation Ultrasound | Surgical navigation IOM Brain stimulator Ultrasonic aspirator Intraoperative MRI |
Medications | Steroids Antiepileptics 5-ALA or Fluorescein | Antiepileptics | Steroids | Steroids Antiepileptics |
Anatomic considerations | Sylvian fissure, speech and motor areas, lateral ventricle | Corpus callosum, MCA | Sphenoid wing, frontal sinus, sagittal sinus, Broca area, lateral ventricles, ACA | Coronal suture, IFG, orbital gyrus, frontal horn lateral ventricle, caudate head, fornix, ventral striatal pallidum, anterior perforated substance, mesial basal frontal cortex, genu of corpus callosum, prefrontal veins and arteries |
Complications feared with approach chosen | Language dysfunction, motor deficit | Language dysfunction | Language dysfunction, ACA injury | Language dysfunction, motor deficit, cognitive dysfunction |
Intraoperative | ||||
Anesthesia | Asleep-awake-asleep | General | General | Awake (MAC) |
Skin incision | Bicoronal | Bicoronal | Modified bicoronal | Bicoronal linear |
Bone opening | Left frontal near sagittal sinus | Left frontal | Left frontal above frontal sinus | Left frontal |
Brain exposure | Left SFG, MFG, IFG | Left frontal | Left frontal pole | Left SFG, MFG, IFG |
Method of resection | Local anesthetic application, craniotomy planning based on navigation, large left frontal craniotomy to encompass lesion and Sylvian fissure, cruciate dural opening over lesion, patient awoken, ECoG grids, awake speech and motor mapping, outline tumor with navigation, corticectomy in negative mapping areas starting lateral to tumor, dissect posteriorly and leave medial portion for last, extend resection to skull base and into frontal horn of lateral ventricle, debulk tumor with ultrasonic aspirator, dissect from critical white matter tracts identified during mapping, ultrasound to guide further resection, resect fluorescing tissue, watertight dural closure | Craniotomy based on navigation, open dura, delineate tumor margins with navigation and ultrasound, attempt en bloc, inspect cavity with 5-ALA and ultrasound | Semibicoronal incision taken down to just temporalis fascia, craniotomy ipsilateral to sagittal sinus, ultrasound to locate hyperechoic component, intralesional resection, remove as much of the suckable portion of tumor as possible, no attempt at en bloc or supratotal resection | Craniotomy based on navigation, dural opening, identify and protect the Broca area, resection from lateral fissure to intercerebral fissure to 2 cm in front of coronal suture and close to the frontal horn of the lateral ventricle, attempt to avoid opening lateral ventricle, removal of the prefrontal lobe en bloc with ultrasonic aspirator, removal of deep portion of residual tumor guided by navigation, continuous MEP, intraoperative MRI to guide further resection, watertight dural closure |
Complication avoidance | Cortical and subcortical mapping, leave medial portion for last, fluorescence, ultrasound | Attempt en bloc, 5-ALA and ultrasound to guide resection | Ultrasound, limiting resection to suckable component | Cortical and subcortical mapping, continuous MEP, obey anatomic boundaries, intraoperative MRI |
Postoperative | ||||
Admission | ICU | ICU | Intermediate care | ICU |
Postoperative complications feared | Language dysfunction, motor deficit, seizures | Language dysfunction | Language dysfunction, vascular injury | Language dysfunction, cognitive disorder |
Follow-up testing | MRI within 48 hours after surgery | MRI within 48 hours after surgery | MRI within 24 hours after surgery Neuropsychological and speech assessment 3 days after surgery | Intraoperative MRI on completion of surgery or MRI within 72 hours after surgery |
Follow-up visits | 7 days after surgery | 3–4 weeks after adjuvant therapy | 7 days after surgery 1 month after surgery with MRI | 1 month 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–radiation/temozolomide Wild type–radiation/temozolomide |
MGMT status | Methylated–radiation/temozolomide Unmethylated–radiation/temozolomide | Methylated–radiation/temozolomide Unmethylated–radiation/temozolomide | Methylated–radiation/temozolomide Unmethylated–radiation/temozolomide | Methylated–radiation/temozolomide Unmethylated–radiation/temozolomide |

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