Difference between revisions of "Myxopapillary ependymoma"

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| Micro      = Papillary tumor cells around vascular myxoid matrix
| Micro      = Papillary tumor cells around vascular myxoid matrix
| Subtypes  = subtype of [[ependymoma]]
| Subtypes  = subtype of [[ependymoma]]
| LMDDx      = [[ependymoma]]
| LMDDx      = [[chordoma]], [[myxoid chondrosarcoma]], [[paraganglioma]], papillary [[adenocarcinoma]]
| Stains    = Alcian blue +ve  
| Stains    = Alcian blue +ve  
| IHC        = GFAP +ve
| IHC        = GFAP +ve
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==Gross==
==Gross==
*soft.
*Soft.
*gray.
*Gray.
*discrete masses.  
*Discrete masses.  
*often encapsulated.
*Often encapsulated.
*Subtotal resected tumors may spread throughout the neuraxis.
*Subtotal resected tumors may spread throughout the neuraxis.


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</gallery>
</gallery>


==Histology==
==Microscopic==
Features:
Features:
*Papillary appearance.
*Papillary appearance.
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*Microcysts.
*Microcysts.
*Low mitotic activity.
*Low mitotic activity.


Note:
Note:
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DDx:
DDx:
* [[Chordoma]]
* [[Chordoma]].
* [[Myxoid chondrosarcoma]]
* [[Myxoid chondrosarcoma]].
* [[Paraganglioma]]
* [[Paraganglioma]].
* Papillary [[Adenocarcinoma]]
* Papillary [[adenocarcinoma]].
Images:


===Images===
<gallery>
<gallery>
File:Myxopapillary_ependymoma.jpg | Mxyopapillary Ependymoma, HE Smear (AFIP)
File:Myxopapillary_ependymoma.jpg | Mxyopapillary Ependymoma, HE Smear (AFIP)
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==Molecular==
==Molecular==
* Poorly characterized
* Poorly characterized.
* No consistent abberations.
* No consistent abberations.


==See also==
==See also==

Revision as of 16:05, 27 April 2015

Myxopapillary ependymoma
Diagnosis in short

Myxopapillary ependymoma. H&E stain

LM Papillary tumor cells around vascular myxoid matrix
Subtypes subtype of ependymoma
LM DDx chordoma, myxoid chondrosarcoma, paraganglioma, papillary adenocarcinoma
Stains Alcian blue +ve
IHC GFAP +ve
Site usually lumbar spinal cord

Prognosis good (WHO Grade I)

Mxyopapillary Ependymoma, is a low-grade Ependymoma. It is nearly always associated with cauda equina and filum terminale.

General

  • Low-grade ependymoma - WHO Grade I by definition.
  • Classically in the spinal cord of adults.
  • Approx 9-13% of all ependymal tumors.[1]
  • Associated with back pain.
  • Enhancing mass

Gross

  • Soft.
  • Gray.
  • Discrete masses.
  • Often encapsulated.
  • Subtotal resected tumors may spread throughout the neuraxis.

Microscopic

Features:

  • Papillary appearance.
  • Perivascular pseudorosettes:
    • Cuboidal to elongated tumor cells.
    • Radially arranged around vascular cores.
  • Myxoid material surround blood vessels.
  • Microcysts.
  • Low mitotic activity.

Note: Cases with extensive sclerosis may mimic degenerative changes. [2]

DDx:

Images

IHC

  • GFAP+ve.
  • S-100+ve.
  • MIB-1 <1%.

Molecular

  • Poorly characterized.
  • No consistent abberations.

See also

References

  1. Schiffer, D.; Chiò, A.; Giordana, MT.; Migheli, A.; Palma, L.; Pollo, B.; Soffietti, R.; Tribolo, A. (Aug 1991). "Histologic prognostic factors in ependymoma.". Childs Nerv Syst 7 (4): 177-82. PMID 1933913.
  2. Schittenhelm, J.; Becker, R.; Capper, D.; Meyermann, R.; Iglesias-Rozas, JR.; Kaminsky, J.; Mittelbronn, M.. "The clinico-surgico-pathological spectrum of myxopapillary ependymomas--report of four unusal cases and review of the literature.". Clin Neuropathol 27 (1): 21-8. PMID 18257471.