CNS Tumors Flashcards
What is the typical clinical setting of diffuse and anaplastic astrocytoma?
Diffuse:
Anaplastic:
What are the general differences between metastasis to the brain and from other primary rumors and primary brain tumors?
Primary - poorly circumscribed, single, location varies
Secondary - well circumscribed, often multiple, location usually located in the junction between gray and white matter
What is the morphological appearance of diffuse and anaplastic astrocytoma?
Diffuse: diffuse, large area
Astrocytoma:
What is the Histologically appearance of diffuse and anaplastic astrocytoma?
Diffuse: more cellular, some holes, infiltrative, fibriles, start seeing pleomorphic, gemistocytic (only some)
Anaplastic: more cellular, more pleomorphism, GFAP more, mitotic figure (specific stain) split,
What are the genetic changes of diffuse and anaplastic astrocytoma?
Diffuse: don’t do well in survival,
Astrocytoma:
What is the prognosis of of diffuse and anaplastic astrocytoma?
Diffuse: greater than 5 years
Anaplastic: 2-3 years
How do glioblastoma and pilocytic astrocytoma differe clinically?
Pilocytic: not a whole lot
Glioblastoma: slowly progressive neuro deficit, usually motor weakness, increased ICP, nausea, vommiting, seizures, butterfly, bilateral quadriplegia
How do glioblastoma and pilocytic astrocytoma differe Histologically?
Pilocytic:
Glioblastoma: pseudopalisading necrosis, cross midline, serpentine necrosis, tumor cells escapes necrosis
What is the WHO grading for I-IV grade CNS tumors?
Determined by histology
Grade I: low poliferative potential (meningiomas), can resect
Grade II: infiltrative, low proliferation, cannot resect
Grade III: generally Histologically evidence of malignancy (nuclear atypia, pliomorphic, mitotic)
Grade IV: cytologically malignant, mitotically active, necrosis prone (in center). Vessels and actively growing.
What are the clinical and morphological features of oligodendroglioma?
Clinical: les common, seizures
Morphologically: calcifications (dark irregular shapes, fall out), fired egg look, perinuclear halo
-squash prep showing vascular it
Genetic: 1p and 19q arm deletion
What are the clinical and morphological features of ependyoma?
Clinical: children in brain, adult in spinal cord, slow growing but 4 yr prognosis, if spread hey go to spinal cord, CSF dissemination
Morphologically: massive, no necrosis or blood supply, very disorganized
What are the clinical, genetic, and morphological features of medulloblastoma?
Clinical: children, cerebellum, radiosensitive, headache, worsening vommiting, back pain and motion sickness
Morphological: well circumscribed
Genetic: i(17q10) = poor
Histologically: small, dark cells, elongated, anaplastic, homer- wright rosettes
More predominant in males
What are the clinical and morphological features of meningioma?
Clinical: slow-growing, benign, of arachnoid cells
Morphological:mat thatched to dura, compressed brain, syncytial pattern, psammoma bodies
Second most common primary brain tumor
What are the four types of rosettes commonly found in brain tumors?
Also called canal
- Vascular pseudo rosette (blood vessel)
- Homer- wright - protein in the center
- Flexner - Wintersreiner (Rb) -
4.
What are the three gliomas?
- astrocytoma
- oligodendroglioma
- ependdyoma
What percent of CNS tumors are metastic from another site?
70%
What are the two most common tumors?
GMF
Meningioma
What percent of tumors spread to the brain?
25-50%
Lung, melanoma, breast
What are sometimes the first sign of the primary tumor?
Meningeal carcinomatosi- tumor studding the surface of the brain
Little studs
What do metastatic tumors look like Histologically?
Infiltration
Pliomorphic
Follow path of least resistance
What are the most common brain cancers in children?
Medulloblastoma
Astrocytoma
CNS tumors are 27% of CNS tumors in children
(Second leading cause of tumors)
What is adjuvant treatment?
If the treatment follows the primary treatment (chemo, radiation, tumor)
Tries to get rid of residual cancer cells
Where are most tumors located in children and adults?
Children: 70% in PF
Adults: 70% in ST (hemispheric)
What is part of the prognosis other than grade?
Age Location Performance (therapy can cause brain damage) Radiological features Extent of resection Proliferation index Genetic alterations