Sexcord/ stromal ovarian tumors classification: Difference between revisions

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==Classification==
==Classification==
 
WHO classification for ovarian sex cord-stromal tumors:
'''Pure stromal tumors'''
* Fibroma
* Cellular fibroma
* Thecoma
* Luteinized thecoma associated with sclerosing peritonitis
* Fibrosarcoma
* Sclerosing stromal tumor
* Signet-ring stromal tumor
* Microcystic stromal tumor
* Leydig cell tumor
* Steroid cell tumor
* Steroid cell tumor, malignant
{| class="wikitable"
{| class="wikitable"
|+WHO classification scheme for ovarian sex cord-stromal tumors<ref name="pmid26054417">{{cite journal |vauthors=Horta M, Cunha TM |title=Sex cord-stromal tumors of the ovary: a comprehensive review and update for radiologists |journal=Diagn Interv Radiol |volume=21 |issue=4 |pages=277–86 |date=2015 |pmid=26054417 |pmc=4498422 |doi=10.5152/dir.2015.34414 |url=}}</ref>
|+WHO classification scheme for ovarian sex cord-stromal tumors<ref name="pmid26054417">{{cite journal |vauthors=Horta M, Cunha TM |title=Sex cord-stromal tumors of the ovary: a comprehensive review and update for radiologists |journal=Diagn Interv Radiol |volume=21 |issue=4 |pages=277–86 |date=2015 |pmid=26054417 |pmc=4498422 |doi=10.5152/dir.2015.34414 |url=}}</ref>

Revision as of 16:37, 7 March 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Overview

There is no established system for the classification of [disease name].

OR

[Disease name] may be classified according to [classification method] into [number] subtypes/groups: [group1], [group2], [group3], and [group4].

OR

[Disease name] may be classified into [large number > 6] subtypes based on [classification method 1], [classification method 2], and [classification method 3]. [Disease name] may be classified into several subtypes based on [classification method 1], [classification method 2], and [classification method 3].

OR

Based on the duration of symptoms, [disease name] may be classified as either acute or chronic.

OR

If the staging system involves specific and characteristic findings and features: According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2].

OR

The staging of [malignancy name] is based on the [staging system].

OR

There is no established system for the staging of [malignancy name].

Classification

WHO classification for ovarian sex cord-stromal tumors: Pure stromal tumors

  • Fibroma
  • Cellular fibroma
  • Thecoma
  • Luteinized thecoma associated with sclerosing peritonitis
  • Fibrosarcoma
  • Sclerosing stromal tumor
  • Signet-ring stromal tumor
  • Microcystic stromal tumor
  • Leydig cell tumor
  • Steroid cell tumor
  • Steroid cell tumor, malignant
WHO classification scheme for ovarian sex cord-stromal tumors[1]
Types Subtypes
Pure stromal tumors
  • Fibroma
  • Cellular fibroma
  • Thecoma
  • Luteinized thecoma associated with sclerosing peritonitis
  • Fibrosarcoma
  • Sclerosing stromal tumor
  • Signet-ring stromal tumor
  • Microcystic stromal tumor
  • Leydig cell tumor
  • Steroid cell tumor
  • Steroid cell tumor, malignant
Pure sex cord tumors
  • Adult granulosa cell tumor
  • Juvenile granulosa cell tumor
  • Sertoli cell tumor
  • Sex cord tumor with annular tubules
Mixed sex cord-stromal tumors
  • Sertoli-Leydig cell tumors
    • Well-differentiated
    • Moderately differentiated with heterologous elements
    • Poorly differentiated with heterologous elements
    • Retiform with heterologous elements
  • Sex cord-stromal tumours, NOS

References

  1. Horta M, Cunha TM (2015). "Sex cord-stromal tumors of the ovary: a comprehensive review and update for radiologists". Diagn Interv Radiol. 21 (4): 277–86. doi:10.5152/dir.2015.34414. PMC 4498422. PMID 26054417.

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