Astrocytoma differential diagnosis

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Fahimeh Shojaei, M.D.

Differentiating astrocytoma from other Diseases

Diseases		Clinical manifestations							Para-clinical findings				Gold standard	Additional findings
		Symptoms					Physical examination
									Lab Findings	Imaging		Immunohistopathology
		Headache	Seizure	Visual disturbance	Hearing loss	Constitutional	Extraocular movement disorder	Focal neurologic deficit	Endocrine abnormalities	CT scan	MRI
Adult primary brain tumors	Glioblastoma multiforme	+	+/−	+/−	−	−		+	−		Supratentorial Irregular ring-nodular enhancing lesions Central necrosis Surrounding vasogenic edema Cross corpus callosum (butterfly glioma)	Astrocyte origin Pleomorphic cell Pseudopalisading appearance GFAP + Necrosis + Hemorrhage + Vascular prolifration +	Biopsy	Highest incidence in fifth and sixth decades of life Most of the time, focal neurological deficit is the presenting sign.
	Oligodendroglioma	+	+	+/−	−	−		+	−		Almost always in cerebral hemisphers (frontal lobes) Hypointense on T1 Hyperintense on T2 Calcification Chicken wire capillary pattern	Oligodendrocyte origin Calcification + Fried egg cell appearance	Biopsy	Highest incidence is between 40 and 50 years of age. Most of the time, epileptic seizure is the presenting sign.
	Meningioma	+	+/−	+/−	−	−		+	−		Well circumscribed Extra-axial mass Dural attachment CSF vascular cleft sign Sunburst appearance of the vessels	Arachnoid origin Psammoma bodies Whorled spindle cell pattern	Biopsy	Highest incidence is between 40 and 50 years of age. Most of the time, focal neurological deficit and epileptic seizure are the presenting signs. May be associated with NF-2
	Hemangioblastoma	+	+/−	+/−	−	−		+	−		Infratentorial Cystic lesion with a solid enhancing mural nodule	Blood vessel origin Capillaries with thin walls	Biopsy	Might secret erythropoietin and cause polycythemia May be associated with von hippel-lindau syndrome
	Pituitary adenoma	−	−	+ Bitemporal hemianopia	−	−		−	Endocrine abnormalities as a result of functional adenomas or pressure effect of non-functional adenomas		Isointense to normal pituitary gland in T1	Endocrine cell hyperplasia	Biopsy	Initialy presents with upper bitemporal quadrantanopsia followed by bitemporal hemianopsia (pressure on optic chiasma from below)
	Schwannoma	−	−	+/−	+	−			−		Split-fat sign Fascicular sign Often have areas of hemosiderin	Schwann cell origin S100+	Biopsy	May be associated with NF-2 (bilateral schwannomas)
	Primary CNS lymphoma	+	+/−	+/−	−	−			−		Usually deep in the white matter Single mass with ring enhancement	B cell origin Similar to non hodgkin lymphoma (diffuse large B cell)	Biopsy	Usually in young immunocompromized patients (HIV) or old immunocompetent person.
Childhood primary brain tumors	Pilocytic astrocytoma	+	+/−	+/−	−	−			−		Infratentorial Solid and cystic component Mostly in posterior fossa Usually in cerebellar hemisphers and vermis	Glial cell origin Solid and cystic component GFAP +	Biopsy	Most of the time, cerebellar dysfunction is the presenting signs.
	Medulloblastoma	+	+/−	+/−	−	−			−		Infratentorial Mostly in cerebellum Non communicating hydrocephalus	Neuroectoderm origin Homer wright rosettes	Biopsy	Drop metastasis ( metastasis through CSF)
	Ependymoma	+	+/−	+/−	−	−			−		Infratentorial Usually found in 4th ventricle Mixed cystic/solid lesion Hydrocephalus	Ependymal cell origin Perivascular pseudorosette	Biopsy	Causes an unusually persistent, continuous headache in children.
	Craniopharyngioma	+	+/−	+ Bitemporal hemianopia	−	−			Hypopituitarism as a result of pressure effect on pituitary gland		Calcification Lobulated contour Motor-oil like fluid within tumor	Ectodermal origin (Rathkes pouch) Calcification +	Biopsy	Initialy presents with lower bitemporal quadrantanopsia followed by bitemporal hemianopsia (pressure on optic chiasma from above)
	Pinealoma	+	+/−	+/−	−	−	+ vertical gaze palsy	+	+ B-hCG rise leads to precocious puberty in males		Hydrochepalus (compression of cerebral aqueduct)	Similar to testicular seminoma	Biopsy
Vascular	AV malformation	+	+			−				Bag of worms" appearance in CT angiography	Supratentorial: ~85% Flow voids on T2 weighted images	We do not perform biopsy for AVM	Angiography
	Brain aneurysm	+				−							Magnetic resonance angiography and CT angiography (Angiographjy is reserved for patients who have negative MRA and CTA)	It is associated with autosomal dominant polycystic kidney disease, Ehlers-Danlos syndrome, pseudoxanthoma elasticum and Bicuspid aortic valve.
Infectious	Bacterial brain abscess	+				+					Central hypodense signal and surrounding ring-enhancement in T1 Central hyperintense area surrounded by a well-defined hypointense capsule with surrounding edema in T2
	Tuberculosis	+				+
	Toxoplasmosis	+									Multifocal masses with ring enhancement Mostly in basal ganglia, thalami, and corticomedullary junction.
	Hydatid cyst	+									Honeycomb appearance Necrotic area
	Fungal	+
Other	Brain metastasis	+									Multiple lesions Vasogenic edema	Based on the primary cancer type we may have different immunohistopathology findings.	History/ imaging If there is any uncertainty about etiology, biopsy should be performed	Most common primary tumors that metastasis to brain: Lung cancer Renal cell carcinoma Breast cancer Melanoma Gastrointestinal tract