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Central Nervous System Tumors
Overview of CNS Tumors
CNS tumors can be metastatic (50%) or primary (50%).
Common Metastatic Sources:
Lung cancer
Breast cancer
Kidney cancer
Presentation: Metastatic lesions often appear as multiple well-circumscribed lesions, primarily at the gray-white junction.
Classification of Primary CNS Tumors
Primary CNS tumors are classified by cell type:
Malignant primary tumors are typically locally destructive, but do not usually spread outside CNS.
Cell Types in CNS
CNS consists of:
50% Neurons
50% Glial Tissue (supports neurons)
Astrocytes: Form the blood-brain barrier.
Oligodendrocytes: Myelinate axons.
Ependymal Cells: Line the ventricular spaces.
Meningothelial Cells: Surround the brain.
These cell types can produce tumors in both children and adults.
Key Tumors in CNS
Astrocytic Tumors
Pilocytic Astrocytoma:
Description: Benign tumor in children.
Location: Usually in the cerebellum.
Key Imaging: Cystic lesion with a mural nodule.
Histological Features: Rosenthal fibers (thick eosinophilic processes).
GFAP Positive.
Glioblastoma Multiforme:
Description: Highly malignant tumor in adults; most common CNS tumor.
Location: Cerebral hemispheres.
Characteristic Association: Crosses the corpus callosum; sometimes called butterfly glioma.
Histological Features:
Necrosis: Large necrotic areas.
Pseudo Palisading: Living cells at the edge of necrosis.
Endothelial Cell Proliferation.
Intermediate Filament: GFAP positive.
Oligodendrocytic Tumors
Oligodendroglioma:
Description: Malignant tumor of oligodendrocytes.
Key Features: Often calcified tumor in the white matter (frontal lobe) that typically presents with seizures.
Histological Features: Fried egg appearance (cytoplasm resembles fried eggs).
Ependymal Tumors
Ependymoma:
Description: Malignant tumor from ependymal cells (childhood)
Location: Usually in the fourth ventricle, grows into ventricular space blocking CSF flow, leading to hydrocephalus.
Histological Features: Perivascular pseudorosettes.
Meningeal Tumors
Meningioma:
Description: Benign tumor of arachnoid cells; most common benign tumor in adults.
Demographics: Predominantly seen in adult females.
Key Features: Attached to dura, compresses cortex causing seizures (compression, not invasion).
Histological Features: Whorled pattern (often with calcified somoma bodies).
Neuroectodermal Tumors
Medulloblastoma:
Description: Malignant tumor derived from granular cells of the cerebellum, often seen in children.
Histological Features: Small round blue cells with Homer-Wright rosettes; rapid growth, poor prognosis, drop metastases through CSF.
Craniopharyngioma
Description: Tumor from Rathke’s pouch remnants; occurs in children and young adults.
Location: Supratentorial mass (near optic chiasm).
Symptoms: Can cause bitemporal hemianopsia due to optic chiasm compression.
Imaging: Often calcified; benign but may recur after resection.