Difference between revisions of "Neuropathology tumours"

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Update of rare entities of uncertain origin.
(Update of rare entities of uncertain origin.)
Line 328: Line 328:
*Abbreviated ''ETANTR''.
*Abbreviated ''ETANTR''.
{{Main|Embryonal tumour with abundant neuropil and true rosettes}}
{{Main|Embryonal tumour with abundant neuropil and true rosettes}}
==Astroblastoma==
*No WHO grade yet.
*Very rare superficial tumor of young age.
*Large, cystic. Pushing margin towards CNS.
*Vasocentric growth, plump cells with absence of fibrillary pattern.
*GFAP+ve, Synaptohysin-ve, focally EMA/panCK+ve. MIB-1: 1-18 %.
<gallery>
File:Astroblastoma_HE_Specimen.jpg | HE. (WC/jensflorian)
File:Astroblastoma_HE_papillae.jpg | HE. (WC/jensflorian)
File:Astroblastoma.jpg | Astroblastoma (AFIP)
</gallery>
==Chordoid glioma of the 3rd ventricle==
* WHO grade II.
* Slowly growing, non-invasive.
* Clusters of epithelioid cells in mucinous stroma.
* Lymphocytic infiltrates, adjacent Rosenthal fibers.
* Few mitoses.
* GFAP+ve,  MIB-1 1-3%.
==Angiocentric glioma==
*Grade I WHO neuroepithelial tumor.
{{Main|Angiocentric glioma}}


==CNS lymphoma==
==CNS lymphoma==
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