Difference between revisions of "Chordoma"

From Libre Pathology
Jump to navigation Jump to search
Line 58: Line 58:
**Myxopapillary ependymoma.
**Myxopapillary ependymoma.
**[[Myxoid liposarcoma]]  - negative for EMA and cytokeratins.
**[[Myxoid liposarcoma]]  - negative for EMA and cytokeratins.
*Choroid lesions:
*Chordoid lesions:
**[[Choroid meningioma]].
**[[Chordoid meningioma]].
**Choroid glioma - location, location, location.
**Chordoid glioma<ref>{{Cite journal  | last1 = Zarghouni | first1 = M. | last2 = Vandergriff | first2 = C. | last3 = Layton | first3 = KF. | last4 = McGowan | first4 = JB. | last5 = Coimbra | first5 = C. | last6 = Bhakti | first6 = A. | last7 = Opatowsky | first7 = MJ. | title = Chordoid glioma of the third ventricle. | journal = Proc (Bayl Univ Med Cent) | volume = 25 | issue = 3 | pages = 285-6 | month = Jul | year = 2012 | doi =  | PMID = 22754136 }}</ref> - location, location, location.
**Large notochordal rest - only evidence of destructive growth can identify a chordoma.
**Large notochordal rest - only evidence of destructive growth can identify a chordoma.
*[[Metastasis]]:
*[[Metastasis]]:
**Metastatic [[signet ring cell carcinoma]] - negative for S100 and brachyury; clinical history (important).
**Metastatic [[signet ring cell carcinoma]] - negative for S100 and brachyury, [[clinical history]] (important).
**Metastatic [[clear cell renal cell carcinoma]] - negative for S100 and brachyury; clinical history (important).
**Metastatic [[clear cell renal cell carcinoma]] - negative for S100 and brachyury, clinical history (important).
*[[Parachordoma]] - extremely rare.
*[[Parachordoma]] - extremely rare.



Revision as of 17:16, 4 December 2014

Chordoma
Diagnosis in short

Chordoma. HPS stain.

LM physaliphorous cells (also bubble cells) - very large clear bubble with a sharp border, bubble does not compress nucleus; islands of cells surrounded by fibrous tissue; myxoid background
LM DDx chondrosarcoma, myxoid lesions, parachordoma
IHC S-100 +ve, AE1/AE3 +ve, Brachyury +ve, EMA +ve
Gross myxoid
Site sacrum or clivus

Prevalence uncommon

Chordoma is an uncommon tumour in neuropathology.

General

  • Location: usually sacrum or clivus.
  • It is a bone tumour.

Gross

  • Soft, gelatinous, lobulated.[1]

DDx:

  • Bony metastasis (mucinous carcinoma) - typically multifocal.

Image:

Microscopic

Features:[2]

  • Architecture: islands of cells surrounded by fibrous tissue.
    • Also described as "lobulated" architecture; may not be apparent.
  • Myxoid background - grey extracellular material, variable amount present.
  • Mixed cell population:
    1. Abundant eosinophilic cytoplasm.
    2. Physaliphorous cells or bubble cells - key feature.
      • Have a very large clear bubble with a sharp border; bubble does not compress nucleus - nucleus may be in bubble.

DDx:

Images

www:

IHC

Features:[4][5]

  • S-100 +ve.
  • AE1/AE3 +ve.
  • Brachyury +ve -- key stain.
    • Protein important for axial development, affects notochord development.[6]
    • Brachyury literally means short tail.[7]
  • EMA +ve.

Key points:

  • Brachyury is not a commonly stocked antibody.
  • Chordoma will be S100 AND Epithelial marker positive.
  • Many other items in the DDX will be either S100 OR Epithelial marker positive.

See also

References

  1. URL: http://www.histopathology-india.net/Chordoma.htm. Accessed on: 12 April 2012.
  2. Tadrous, Paul.J. Diagnostic Criteria Handbook in Histopathology: A Surgical Pathology Vade Mecum (1st ed.). Wiley. pp. 184. ISBN 978-0470519035.
  3. Zarghouni, M.; Vandergriff, C.; Layton, KF.; McGowan, JB.; Coimbra, C.; Bhakti, A.; Opatowsky, MJ. (Jul 2012). "Chordoid glioma of the third ventricle.". Proc (Bayl Univ Med Cent) 25 (3): 285-6. PMID 22754136.
  4. URL: http://path.upmc.edu/cases/case312/micro.html. Accessed on: 14 January 2012.
  5. Coindre, JM.; Rivel, J.; Trojani, M.; De Mascarel, I.; De Mascarel, A. (Sep 1986). "Immunohistological study in chordomas.". J Pathol 150 (1): 61-3. doi:10.1002/path.1711500110. PMID 2431128.
  6. Online 'Mendelian Inheritance in Man' (OMIM) 601397
  7. URL: http://www.jstor.org/pss/86845. Accessed on: 18 May 2010.