CNS-Tumors Flashcards

1
Q

General Properties (Brain tumors)

A
  • 30 % become metastatic
  • 70% of adult neoplasms=Supratentorial
  • 70% of child neoplasms=Infratentorial (cerebellum)
  • _Common highly malignant adult tumo_r=Gilblastoma multiforme
  • Common malignant tumor in children=<strong>Medullablastoma</strong>
  • Primary neurologlial tumor (gilomas)-
    • Astrocytoma & oligodendroglioma
  • Primitive neuroeputhelial tumor- Medulloblastoma
  • Neuronal tumor-Lymphoma
  • Meningioma (arachnoid cells)
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2
Q

Pilocystic Astrocytoma

A
  • Genetics- TP53
  • Marker-GFAP (glial fibrillary acidic protein)
    • <strong><u>Fibrillary astrocytic astrocytoma</u></strong>-<em><strong>Anti-GFAP</strong></em>
  • Pilocystic Astrocytoma-Children (benign)
    • Cystic mass w/mural nodule in cerebellum
    • _Other-_3rd vent or optic nerve
  • Histo: Rosenthal fibers (eosinophilic)
  • Found in Cerebellum good prognosis w/removal
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3
Q

Glioblastoma Multiforme (astrocyte)

A
  • Common in adults & very agressive (cortex)
    • Crosses corpus collosum (midline)
  • **Seizures w/motor weakness **
  • Area of necrosis-area of malignancy
    • Neoplastic cells surround it (pseudo-palasading)
    • Can be seen in MRI
    • High mitotic index
    • HIgh vascular proliferation
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4
Q

Signs/Symptoms of Brain tumors

A
  • Mass effect-Compression of BV & herniation
  • Edema by herniation/masseffect
  • Raised intracranial pressure-Headache
  • Focal abnormality-Seizures
  • Prognosis & Treatment depend on:
    • Location, histo grade, Age (adults worse)
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5
Q

Oligodendroglioma

A
  • Malignant well circumscribed w/cystic areas
  • Focal calcification in white matter-frontal lobe
    • Low frequency of occurence (5%)
  • X-ray-Calcification
    • Craniophryngioma (derived from Ratheke’s pouch)
      • Bi-temporal heminopsia (children)
    • Toxoplasma (Cat scratch)
    • Cytomeglovirus (HPV)
  • Histo: Tumor cells cluster around neurons
    • “Fried egg appearance”
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6
Q

Ependymoma

A
  • Occurence @ any age most common in 1st 20 yrs
    • Commonly seen in children
  • Ventricle-Reveals TRUE rosette pattern
    • Histo: Cells arranged around central vascular space
  • Myxopapillary-Filum terminale of spinal cord (cauda equina)
    • Histo: Myxoid connective tissue core
  • Clinical-Intracranial/ventricle=Hydrocephalous
    • Tumor cells seen in CSF
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7
Q

Medulloblastoma

A
  • Primitive neuroepi neoplasm-malignant children
  • Lesion in cerebellum-Midline vermis=Children
    • Spreads through CSF-Drop metastasis through spinal cord
  • Histo-Homer-Wright rosettes
  • Treatment:
    • Radiotherapy entire spinal cord=70% (5 year survival)
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8
Q

Meningioma

A
  • Benign tumor from meningothelial cells (Arachnoid)
    • Round mass attached to dura
  • Adult Female Pt-Tumor has estrogen receptors
  • Slow growth=**Increase intracranial pressure **
    • <strong>Weakness of limbs & seizures</strong>
  • Histo-
  • Spindle cells in syncytial mass (whorls)
  • Psammoma body-Ca+2 <strong>(papillary carcinoma of thyroid)</strong>
  • Presents w/Neurofibromatosis:
  • Type 1-Neurofibroma, <u>peripheral schwanoma</u>, pigmented skin & iris
  • Type 2-schwanoma of CN8 <u>(hearing loss)</u>, post lens opacification
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9
Q

Acoustic Neuromas/Schwannoma

A
  • Benign neuroma of CN 8
    • S-100 ++ stain
  • Presents @ Cerebellopontine angle
  • Clinical-Hearing loss
    • Seen NF type 2
  • Histo:
    • Antoni A = Verocay bodies
    • Antoni B-Low cellularity
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10
Q

Metastatic tumor

A
  • Border of grey & white matter follows MCA
    • Other location meninges
  • Multiple well circumscribed 1-3 cm lesions
  • Lung is primary site of origin
    • Others Acute lymphoblastic leukemia (cancer of WBCs)
    • Melanoma
  • Meningeal metastasis-Leptomeningeal carcinoma
    • Malignant cells spread from leptomeninges
    • Breast cancer primary site
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