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Chiasmal gliomas: appearance and long-term changes demonstrated by computerized tomography
Journal of Neurosurgery
|August 1, 1986
Summary
Computerized tomography (CT) identifies distinct patterns for diagnosing chiasmal gliomas. CT aids neurosurgical treatment, but biopsy is needed to differentiate tumor types.
Area of Science:
- Neuro-oncology
- Radiology
- Ophthalmology
Background:
- Chiasmal gliomas represent a spectrum of lesions affecting the optic nerve and chiasm.
- Accurate diagnosis and treatment planning are crucial for managing these tumors.
Purpose of the Study:
- To evaluate the diagnostic utility of computerized tomography (CT) in characterizing chiasmal gliomas.
- To correlate CT findings with clinical presentation, tumor growth, and treatment outcomes.
Main Methods:
- Retrospective analysis of 22 cases of chiasmal gliomas.
- Detailed review of computerized tomography (CT) scans to identify characteristic patterns.
- Correlation of imaging findings with histological diagnoses and clinical data.
Main Results:
- Three CT patterns were diagnostic: tubular thickening of the optic nerve/chiasm, suprasellar tumor with optic nerve expansion, or optic tract involvement.
- Globular suprasellar tumors without these features required histological examination.
- CT documented tumor growth in only globular-type gliomas; visual function was not a reliable indicator of growth.
- Neurofibromatosis was associated with tubular optic nerve thickening and unilateral optic nerve expansion.
- Radiation therapy led to tumor shrinkage in five cases, with complications including calcification and infarcts.
- CT could not differentiate between juvenile pilocytic astrocytoma and anaplastic astrocytoma.
Conclusions:
- Computerized tomography (CT) is instrumental in diagnosing and guiding the neurosurgical management of chiasmal gliomas.
- CT findings help determine the necessity for biopsy or ventricular shunting.
- Histological examination remains essential for specific tumor type differentiation.