Difference between revisions of "Follicular dendritic cell sarcoma"

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*Muscle-specific actin +ve/-ve.
*Muscle-specific actin +ve/-ve.
*EMA +ve/-ve.
*EMA +ve/-ve.
Additional stains:<ref name=pmid21055030>{{Cite journal  | last1 = Yin | first1 = WH. | last2 = Yu | first2 = GY. | last3 = Ma | first3 = Y. | last4 = Rao | first4 = HL. | last5 = Lin | first5 = SX. | last6 = Shao | first6 = CK. | last7 = Liang | first7 = Q. | last8 = Guo | first8 = N. | last9 = Chen | first9 = GQ. | title = [Follicular dendritic cell sarcoma: a clinicopathologic analysis of ten cases]. | journal = Zhonghua Bing Li Xue Za Zhi | volume = 39 | issue = 8 | pages = 522-7 | month = Aug | year = 2010 | doi =  | PMID = 21055030 }}</ref>
*CD23 +ve.
*D2-40 +ve.


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

Revision as of 21:25, 7 December 2017

Follicular dendritic cell sarcoma
Diagnosis in short

Synonyms follicular dendritic cell tumour, follicular dendritic cell neoplasm

LM oval or spindle-shaped cellular & nuclear morphology, variable architecture (sheets, fascicles, whorles, storiform pattern), nuclei with small nucleoli and clear or dispersed chromatin, multinucleated cells, interspersed small lymphocytes, +/-necrosis, +/-marked nuclear atypia, +/-abundant mitoses.
LM DDx histiocytic sarcoma, thymoma, other spindle cell lesions
IHC CD21 +ve, CD35 +ve, Ki-M4p +ve, Ki-FDRC1p +ve, vimentin +ve
Associated Dx Castleman disease, hyaline-vascular type
Prevalence very rare
Treatment excision

Follicular dendritic cell sarcoma, abbreviated FDCS, is a very rare malignant tumour.

It is also known as follicular dendritic cell tumour (abbreviated FDCT),[1] and follicular dendritic cell neoplasm.[2]

General

  • Very rare.
  • Behave like a low-grade sarcoma.[3]
  • Reported association with Castleman disease (hyaline-vascular type).[3]

WHO 2001 classification of dendritic cell neoplasms:[4]

  • Langerhans cell histiocytosis.
  • Langerhans cell sarcoma.
  • Interdigitating dendritic cell sarcoma/tumour.
  • Follicular dendritic cell sarcoma/tumour.
  • Dendritic cell sarcoma, not specified otherwise.

Microscopic

Features:[3]

  • Oval or spindle-shaped cellular & nuclear morphology.
  • Variable architecture (sheets, fascicles, whorles, storiform pattern).
  • Nuclei:
    • Small nucleoli.
    • Clear or dispersed chromatin.
  • Multinucleated cells.
  • Interspersed small lymphocytes - distinctive feature.
  • +/-Necrosis.
  • +/-Marked nuclear atypia.
  • +/-Abundant mitoses.

DDx:

Images

IHC

Features:[3]

  • CD21 +ve.
  • CD35 +ve.
  • Ki-M4p +ve
  • Ki-FDRC1p +ve.
  • Vimentin +ve.
  • S-100 +ve/-ve.
  • Muscle-specific actin +ve/-ve.
  • EMA +ve/-ve.

Additional stains:[7]

  • CD23 +ve.
  • D2-40 +ve.

See also

References

  1. 1.0 1.1 Leipsic, JA.; McAdams, HP.; Sporn, TA. (Jun 2007). "Follicular dendritic cell sarcoma of the mediastinum.". AJR Am J Roentgenol 188 (6): W554-6. doi:10.2214/AJR.04.1530. PMID 17515347.
  2. Denning, KL.; Olson, PR.; Maley, RH.; Flati, VR.; Myers, JL.; Silverman, JF. (Apr 2009). "Primary pulmonary follicular dendritic cell neoplasm: a case report and review of the literature.". Arch Pathol Lab Med 133 (4): 643-7. doi:10.1043/1543-2165-133.4.643. PMID 19391666.
  3. 3.0 3.1 3.2 3.3 Perez-Ordoñez, B.; Rosai, J. (May 1998). "Follicular dendritic cell tumor: review of the entity.". Semin Diagn Pathol 15 (2): 144-54. PMID 9606805.
  4. Kairouz, S.; Hashash, J.; Kabbara, W.; McHayleh, W.; Tabbara, IA. (Oct 2007). "Dendritic cell neoplasms: an overview.". Am J Hematol 82 (10): 924-8. doi:10.1002/ajh.20857. PMID 17636477.
  5. Alexiev, BA.; Sailey, CJ.; McClure, SA.; Ord, RA.; Zhao, XF.; Papadimitriou, JC. (2007). "Primary histiocytic sarcoma arising in the head and neck with predominant spindle cell component.". Diagn Pathol 2: 7. doi:10.1186/1746-1596-2-7. PMID 17324277. http://www.diagnosticpathology.org/content/2/1/7.
  6. URL: http://www.npplweb.com/wjsmro/fulltext/2/1. Accessed on: September 13, 2014.
  7. Yin, WH.; Yu, GY.; Ma, Y.; Rao, HL.; Lin, SX.; Shao, CK.; Liang, Q.; Guo, N. et al. (Aug 2010). "[Follicular dendritic cell sarcoma: a clinicopathologic analysis of ten cases].". Zhonghua Bing Li Xue Za Zhi 39 (8): 522-7. PMID 21055030.