Ganglioneuroma overview: Difference between revisions
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==Pathophysiology== | ==Pathophysiology== | ||
==Causes== | ==Causes== | ||
==Differentiating brain tumors from other diseases== | ==Differentiating brain tumors from other diseases== | ||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
==Risk factors== | ==Risk factors== | ||
==Natural History, Complications and Prognosis== | ==Natural History, Complications and Prognosis== | ||
==Diagnosis== | ==Diagnosis== | ||
Revision as of 13:55, 11 September 2015
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Classification
Pathophysiology
Causes
Differentiating brain tumors from other diseases
Epidemiology and Demographics
Risk factors
Natural History, Complications and Prognosis
Diagnosis
Staging
There is no established system for the staging of ganglioglioma.
History and Symptoms
The hallmark of cerebral ganglioglioma is temporal lobe epilepsy.[1] Most common symptoms of spinal cord ganglioglioma include back pain, neck pain, radicular pain, weakness, paresthesia, gait disturbance, and bowel and bladder dysfunction. Less common symptoms of spinal cord ganglioglioma include Brown-Sequard syndrome, acute headache due to subarachnoid hemmorhage, progressive scoliosis, loss of motor function, and frequent falls.[2]
Physical examination
Common physical examination findings of ganglioglioma include weak irregular pulse, hypertension, wide pulse pressure, unilateral pupillary dilatation, abnormal ophthalmic examination, and focal neurological deficits.[3]
Laboratory Findings
There are no diagnostic lab findings associated with ganglioglioma.
X Ray
There are no x-ray findings associated with cerebral ganglioglioma. On x-ray, spinal cord ganglioglioma is characterized by scoliosis, bony remodelling, posterior vertebral body scalloping, and remodelling of the pedicle or posterior arch.[2]
CT
On head CT scan, ganglioglioma is characterized by iso- or hypodense, calcification, bone remodelling, and enhancement of solid non-calcified component.
MRI
On MRI brain, ganglioglioma is characterized by iso- to hypointense solid component on T1, variable contrast enhancement of solid component on T1 C+ (Gd), hyperintense solid component and variable signal in cystic component on T2, and calcification on T2 (GE/SWI).[1] On MRI scan of spinal cord, ganglioglioma is characterized by mixed signal intensity on T1-weighted images, high intensity on T2, patchy enhancement on T1 C+ (Gd), and calcification with low signal blooming on gradient echo.[2]
Ultrasound
There are no ultrasound findings associated with ganglioglioma.
Other imaging findings
There are no other imaging findings associated with ganglioglioma.
Other Diagnostic Studies
There are no other diagnostic studies associated with ganglioglioma.
Treatment
Medical Therapy
Radiotherapy or chemotherapy is not the first-line treatment option for patients with gangliogliomas. Radiation therapy is usually reserved for patients when either incomplete resection is achievable or tumor recurrence occurs.[1]
Surgery
The mainstay of therapy for ganglioglioma is surgery. In the brain, a reasonable resection margin can be achieved with surgery.[1]
References
- ↑ 1.0 1.1 1.2 1.3 Symptoms of ganglioglioma. Dr Henry Knipe and Dr Frank Gaillard et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioglioma
- ↑ 2.0 2.1 2.2 Presentation of spinal cord ganglioglioma. Dr Ayush Goel and Dr Sara Wein et al. Radiopaedia 2015. http://radiopaedia.org/articles/spinal-ganglioglioma
- ↑ Presentation of increased ICP. Patient.info. http://patient.info/doctor/raised-intracranial-pressure