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{{Chondrosarcoma}}
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{{CMG}}; {{AE}} {{Rohan}}
==Overview==
Chondrosarcoma may be classified based on histological findings and location.
==Classification==
==Classification==
===Classification and Grading===
*Chondrosarcoma be classified based on [[Histology|histological findings]] and location.
Physicians grade chondrosarcoma using several criteria, but particularly on how abnormal the cancerous cells appear under the microscope, and the growth rate of the tumors themselves, both of which are directly linked to the propensity of the cancer to invade locally, and to spread widely to distant organs and sites in the body (called [[metastasis]]).


====Grade 1====
===Histological Classification===
*Chondrosarcoma grows relatively slowly, has cells whose [[histological]] appearance is quite similar to cells of normal cartilage.
*Chondrosarcoma may be classified based on [[Histological|histological findings]] into following groups:<ref name="pmid8378694">{{cite journal| author=Raymond E, L'Her P, Jeanbourquin D, Schill H, Jancovici R, Daly JP et al.| title=[Chondrosarcoma of the thoracic wall. Review of the literature apropos of 4 cases]. | journal=Rev Pneumol Clin | year= 1993 | volume= 49 | issue= 1 | pages= 19-25 | pmid=8378694 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8378694  }} </ref><ref name="pmid30559960">{{cite journal| author=Lex JR, Evans S, Stevenson JD, Parry M, Jeys LM, Grimer RJ| title=Dedifferentiated chondrosarcoma of the pelvis: clinical outcomes and current treatment. | journal=Clin Sarcoma Res | year= 2018 | volume= 8 | issue=  | pages= 23 | pmid=30559960 | doi=10.1186/s13569-018-0110-1 | pmc=6293503 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30559960  }} </ref>
*Mostly chondroid matrix, little if any myxoid
*Mild-to-moderate increase of cellularity +/- binucleated cells.
*Have much less aggressive invasive and metastatic properties.
{| align="Left"
|-valign="top"
| [[Image:638px-Myxoid liposarcoma (06).jpg|thumb|350px|Grade 1 - Somewhat cellular cartilage with binucleation]]
|}


====Grade 2====
'''Primary Chondrosarcoma'''
*Intermediate grade chondrosarcoma.
*Chondrosarcoma that arises denovo and comprises of following subtypes:
*Little chondroid matrix. Necrosis and more common prominent myxoid.
**Conventional chondrosarcoma - Low-grade, high-grade, and dedifferentiated chondrosarcoma (90% of all chondrosarcomas)
====Grades 3====
**Clear cell chondrosarcoma (1% of all chondrosarcomas)
*Grade 3 chondrosarcoma is increasingly faster-growing cancer, with more varied and abnormal-looking cells.
**Mesenchymal chondrosarcoma (2% of all chondrosarcomas)
*Characterized by myxoid stroma, nuclear pleomorphism and mitoses.
*Absent chondroid matrix.
*These are much more likely to infiltrate surrounding tissues, [[lymph nodes]], and organs.
====Grade 4====
*Some, but not all, authorities and medical facilities assign a "Grade 4" to the most [[anaplastic]], undifferentiated cartilage-derived tumors.


[[ICD-O]] codes provide a more precise classification of chondrosarcoma. These "subtypes" are derived from, and reflect, both
'''Secondary Chondrosarcoma'''
(a) The topographical location of the tumor
*Chondrosarcoma that arises from [[benign]] [[cartilage]] lesions includes (7% of all chondrosarcomas):
(b) The histological characteristics of the cancerous cartilage cells
**[[Osteochondroma]] (<1% risk of [[malignant]] transfomation)
(c) The makeup of the surrounding matrix material associated with the tumor
**Multiple hereditary exostosis (1-10% risk of [[malignant]] transformation)
**[[Enchondroma|Enchondromas]] (1% risk of [[malignant]] transformation)
**[[Enchondroma|Ollier's disease]] (25-40% risk of [[malignant]] transformation)
**[[Maffucci's disease]](100% risk of [[malignant]] transformation)


* 9220 = Chondrosarcoma NOS ("Not Otherwise Specified")
===Based on Location===
* 9221 = Juxtacortical chondrosarcoma
*Chondrosarcoma may be classified based on location into following groups:<ref name="pmid19411454">{{cite journal| author=Giuffrida AY, Burgueno JE, Koniaris LG, Gutierrez JC, Duncan R, Scully SP| title=Chondrosarcoma in the United States (1973 to 2003): an analysis of 2890 cases from the SEER database. | journal=J Bone Joint Surg Am | year= 2009 | volume= 91 | issue= 5 | pages= 1063-72 | pmid=19411454 | doi=10.2106/JBJS.H.00416 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19411454  }} </ref><ref name="pmid17908885">{{cite journal| author=Skeletal Lesions Interobserver Correlation among Expert Diagnosticians (SLICED) Study Group| title=Reliability of histopathologic and radiologic grading of cartilaginous neoplasms in long bones. | journal=J Bone Joint Surg Am | year= 2007 | volume= 89 | issue= 10 | pages= 2113-23 | pmid=17908885 | doi=10.2106/JBJS.F.01530 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17908885  }} </ref>
* 9231 = Myxoid chondrosarcoma
**Centrally located within the [[medullary cavity]]. (central chondrosarcoma) (70% of all chondrosarcomas)
* 9240 = Mesenchymal chondrosarcoma
**Peripherally located on the surface of bone as a result of [[malignant]] transformation within the [[cartilaginous]] cap. (Peripheral chondrosarcoma) (15% of all chondrosarcomas)
* 9242 = Clear cell chondrosarcoma
* 9243 = Dedifferentiated chondrosarcoma


==References==
{{Reflist|2}}
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==References==
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[[Category:Skeletal disorders]]
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Latest revision as of 15:52, 24 January 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Rohan A. Bhimani, M.B.B.S., D.N.B., M.Ch.[2]

Overview

Chondrosarcoma may be classified based on histological findings and location.

Classification

Histological Classification

Primary Chondrosarcoma

  • Chondrosarcoma that arises denovo and comprises of following subtypes:
    • Conventional chondrosarcoma - Low-grade, high-grade, and dedifferentiated chondrosarcoma (90% of all chondrosarcomas)
    • Clear cell chondrosarcoma (1% of all chondrosarcomas)
    • Mesenchymal chondrosarcoma (2% of all chondrosarcomas)

Secondary Chondrosarcoma

Based on Location

  • Chondrosarcoma may be classified based on location into following groups:[3][4]
    • Centrally located within the medullary cavity. (central chondrosarcoma) (70% of all chondrosarcomas)
    • Peripherally located on the surface of bone as a result of malignant transformation within the cartilaginous cap. (Peripheral chondrosarcoma) (15% of all chondrosarcomas)

References

  1. Raymond E, L'Her P, Jeanbourquin D, Schill H, Jancovici R, Daly JP; et al. (1993). "[Chondrosarcoma of the thoracic wall. Review of the literature apropos of 4 cases]". Rev Pneumol Clin. 49 (1): 19–25. PMID 8378694.
  2. Lex JR, Evans S, Stevenson JD, Parry M, Jeys LM, Grimer RJ (2018). "Dedifferentiated chondrosarcoma of the pelvis: clinical outcomes and current treatment". Clin Sarcoma Res. 8: 23. doi:10.1186/s13569-018-0110-1. PMC 6293503. PMID 30559960.
  3. Giuffrida AY, Burgueno JE, Koniaris LG, Gutierrez JC, Duncan R, Scully SP (2009). "Chondrosarcoma in the United States (1973 to 2003): an analysis of 2890 cases from the SEER database". J Bone Joint Surg Am. 91 (5): 1063–72. doi:10.2106/JBJS.H.00416. PMID 19411454.
  4. Skeletal Lesions Interobserver Correlation among Expert Diagnosticians (SLICED) Study Group (2007). "Reliability of histopathologic and radiologic grading of cartilaginous neoplasms in long bones". J Bone Joint Surg Am. 89 (10): 2113–23. doi:10.2106/JBJS.F.01530. PMID 17908885.

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