Difference between revisions of "Atypical teratoid/rhabdoid tumour"

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{{ Infobox diagnosis
| Name      = {{PAGENAME}}
| Image      =
| Width      =
| Caption    =
| Synonyms  =
| Micro      =
| Subtypes  =
| LMDDx      = [[primitive neuroectodermal tumour]] (PNET), [[medulloblastoma]], [[diffuse astrocytoma]], [[choroid plexus carcinoma]],[[embryonal carcinoma]]
| Stains    =
| IHC        = INI1 -ve, S-100 +ve, EMA +ve, SMA +ve
| EM        =
| Molecular  =
| IF        =
| Gross      =
| Grossing  =
| Site      = [[CNS tumours|CNS]] - typically supratentorial
| Assdx      =
| Syndromes  =
| Clinicalhx = usu. <3 years olds, occasionally adults
| Signs      =
| Symptoms  =
| Prevalence = uncommon - esp. in adults
| Bloodwork  =
| Rads      =
| Endoscopy  =
| Prognosis  = very poor
| Other      =
| ClinDDx    =
| Tx        =
}}
'''Atypical teratoid/rhabdoid tumour''', abbreviated '''AT/RT''', is malignant tumour usually found supratentorially.  
'''Atypical teratoid/rhabdoid tumour''', abbreviated '''AT/RT''', is malignant tumour usually found supratentorially.