Difference between revisions of "Plasma cell neoplasms"

From Libre Pathology
Jump to navigation Jump to search
(create -- split-out from lymphoma)
 
Line 6: Line 6:
*Malignancy derived from the plasma cells.
*Malignancy derived from the plasma cells.
*Prognosis: poor.
*Prognosis: poor.
*Most common primary [[bone tumour]] in adults.


Clinical:<ref name=Ref_PCPBoD8_323>{{Ref PCPBoD8|323}}</ref>
Clinical:<ref name=Ref_PCPBoD8_323>{{Ref PCPBoD8|323}}</ref>

Revision as of 04:19, 1 August 2011

Plasma cell neoplasms arise from plasma cells. They are encountered by anatomical pathologists on occasion.

VL does not tease apart plasma cell myeloma, plasmacytoma and plasma cell neoplasm; the first two of these terms redirect to this article.

General

  • Malignancy derived from the plasma cells.
  • Prognosis: poor.
  • Most common primary bone tumour in adults.

Clinical:[1]

  • Bence Jones protein (urine).
  • Abnormal protein electrophoresis (monoclonal gammopathy, dysproteinemia, paraproteinemia).

Note:

  • Plasmacytoma = histology of multiple myeloma; to diagnose multiple myeloma other (non-pathology) criteria are needed.

Microscopic

Features:

Images:

DDx:

  • Neuroendocrine carcinoma - nucleus often has a plasmacytoid (plasma cell-like) appearance.

IHC

  • Kappa -- usu. slightly stronger than lambda.
  • Lambda.
  • CD56.[3]
    • Also +ve in NK/T cell lymphomas.
  • CD57.
    • Also +ve in T-cell large granular lymphocytic leukemia.[4].
  • CD138.
  • CD38. (???)

Molecular

  • t(4;14)(p16.3;q32.3) / IGH–MMSET.[5]
    • Assoc. with poor prognosis.[6]
  • 13q deletions.[7]

See also

References

  1. Mitchell, Richard; Kumar, Vinay; Fausto, Nelson; Abbas, Abul K.; Aster, Jon (2011). Pocket Companion to Robbins & Cotran Pathologic Basis of Disease (8th ed.). Elsevier Saunders. pp. 323. ISBN 978-1416054542.
  2. URL: http://www.thefreelibrary.com/Dutcher+bodies+in+chronic+synovitis-a083551789. Accessed on: 4 August 2010.
  3. URL: http://www.ncbi.nlm.nih.gov/omim/116930. Accessed on: 31 August 2010.
  4. URL: http://www.nature.com/bmt/journal/v33/n1/full/1704298a.html. Accessed on: 31 August 2010.
  5. Chesi, M.; Nardini, E.; Lim, RS.; Smith, KD.; Kuehl, WM.; Bergsagel, PL. (Nov 1998). "The t(4;14) translocation in myeloma dysregulates both FGFR3 and a novel gene, MMSET, resulting in IgH/MMSET hybrid transcripts.". Blood 92 (9): 3025-34. PMID 9787135.
  6. Keats, JJ.; Reiman, T.; Maxwell, CA.; Taylor, BJ.; Larratt, LM.; Mant, MJ.; Belch, AR.; Pilarski, LM. (Feb 2003). "In multiple myeloma, t(4;14)(p16;q32) is an adverse prognostic factor irrespective of FGFR3 expression.". Blood 101 (4): 1520-9. doi:10.1182/blood-2002-06-1675. PMID 12393535.
  7. Mitchell, Richard; Kumar, Vinay; Fausto, Nelson; Abbas, Abul K.; Aster, Jon (2011). Pocket Companion to Robbins & Cotran Pathologic Basis of Disease (8th ed.). Elsevier Saunders. pp. 317. ISBN 978-1416054542.