Sexcord/ stromal ovarian tumors classification: Difference between revisions
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** Sex cord tumor with annular tubules | ** Sex cord tumor with annular tubules | ||
*'''Mixed sex cord-stromal tumors''' | *'''Mixed sex cord-stromal tumors''' | ||
**Sertoli-Leydig cell tumors | **[[Sertoli-Leydig cell tumour|Sertoli-Leydig cell tumors]] | ||
***Well-differentiated | ***Well-differentiated | ||
***Moderately differentiated with heterologous elements | ***Moderately differentiated with heterologous elements | ||
Line 40: | Line 40: | ||
|'''Pure stromal tumors''' | |'''Pure stromal tumors''' | ||
| | | | ||
* Fibroma | * [[Fibroma]] | ||
* Cellular fibroma | * [[Cellular]] [[fibroma]] | ||
* Thecoma | * [[Thecoma]] | ||
* Luteinized thecoma associated with sclerosing peritonitis | * Luteinized [[thecoma]] associated with sclerosing peritonitis | ||
* Fibrosarcoma | * [[Fibrosarcoma]] | ||
* Sclerosing stromal tumor | * Sclerosing stromal tumor | ||
* Signet-ring stromal tumor | * Signet-ring stromal tumor | ||
* Microcystic stromal tumor | * Microcystic stromal tumor | ||
* Leydig cell tumor | * [[Leydig cell tumor]] | ||
* Steroid cell tumor | * Steroid cell tumor | ||
* Steroid cell tumor, malignant | * Steroid cell tumor, [[malignant]] | ||
|- | |- | ||
|'''Pure sex cord tumors''' | |'''Pure sex cord tumors''' | ||
| | | | ||
* Adult granulosa cell tumor | * [[Granulosa cell tumor|Adult granulosa cell tumor]] | ||
* Juvenile granulosa cell tumor | * [[Granulosa cell tumor|Juvenile granulosa cell tumor]] | ||
* Sertoli cell tumor | * [[Sertoli Cell Tumor|Sertoli cell tumor]] | ||
* Sex cord tumor with annular tubules | * Sex cord tumor with annular [[tubules]] | ||
|- | |- | ||
|'''Mixed sex cord-stromal tumors''' | |'''Mixed sex cord-stromal tumors''' | ||
| | | | ||
* Sertoli-Leydig cell tumors | * [[Sertoli-Leydig cell tumour|Sertoli-Leydig cell tumors]] | ||
** Well-differentiated | ** Well-differentiated | ||
** Moderately differentiated with heterologous elements | ** Moderately differentiated with heterologous elements |
Revision as of 13:34, 2 May 2019
Sexcord/ stromal ovarian tumors Microchapters |
Differentiating Sexcord/ Stromal Ovarian Tumors from other Diseases |
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Treatment |
Case Studies |
Sexcord/ stromal ovarian tumors classification On the Web |
American Roentgen Ray Society Images of Sexcord/ stromal ovarian tumors classification |
Risk calculators and risk factors for Sexcord/ stromal ovarian tumors classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: ; Maneesha Nandimandalam, M.B.B.S.[2]
Overview
Sexcord/ stromal ovarian tumors may be classified according to WHO into 3 subtypes: Pure stromal tumors, pure sexcord tumors, mixed stromal and sexcord tumors. Histological classification of sexcord-stromal ovarian tumors includes granulosa stromal cell tumors, sertoli leydig cell tumors, gynandroblastoma, and unclassified.
Classification
WHO classification for ovarian sex cord-stromal tumors:[1][2][3][4][5]
- 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
- Sertoli-Leydig cell tumors
Types | Subtypes |
Pure stromal tumors |
|
Pure sex cord tumors |
|
Mixed sex cord-stromal tumors |
|
NOS, not otherwise specified.
Types | Subtypes |
Granulosa‐stromal cell tumors |
|
Sertoli–Leydig cell tumors |
|
Gynandroblastoma | No specific subtypes |
Unclassified | No specific subtypes |
International Agency for Research on Cancer Histologic Groups of Ovarian Tumors Classification from International agency for research on cancer is summarized in the table: [2][7][3]
Ovarian tumors |
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References
- ↑ 1.0 1.1 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.
- ↑ 2.0 2.1 2.2 Meinhold-Heerlein I, Fotopoulou C, Harter P, Kurzeder C, Mustea A, Wimberger P, Hauptmann S, Sehouli J (April 2016). "The new WHO classification of ovarian, fallopian tube, and primary peritoneal cancer and its clinical implications". Arch. Gynecol. Obstet. 293 (4): 695–700. doi:10.1007/s00404-016-4035-8. PMID 26894303.
- ↑ 3.0 3.1 3.2 Meinhold-Heerlein I, Fotopoulou C, Harter P, Kurzeder C, Mustea A, Wimberger P, Hauptmann S, Sehouli J (October 2015). "Statement by the Kommission Ovar of the AGO: The New FIGO and WHO Classifications of Ovarian, Fallopian Tube and Primary Peritoneal Cancer". Geburtshilfe Frauenheilkd. 75 (10): 1021–1027. doi:10.1055/s-0035-1558079. PMC 4629993. PMID 26556905.
- ↑ 4.0 4.1 McCluggage WG (August 2011). "Morphological subtypes of ovarian carcinoma: a review with emphasis on new developments and pathogenesis". Pathology. 43 (5): 420–32. doi:10.1097/PAT.0b013e328348a6e7. PMID 21716157.
- ↑ 5.0 5.1 Chen, Vivien W.; Ruiz, Bernardo; Killeen, Jeffrey L.; Cot�, Timothy R.; Wu, Xiao Cheng; Correa, Catherine N.; Howe, Holly L. (2003). "Pathology and classification of ovarian tumors". Cancer. 97 (S10): 2631–2642. doi:10.1002/cncr.11345. ISSN 0008-543X. replacement character in
|last4=
at position 4 (help) - ↑ Fuller, P.J.; Leung, D.; Chu, S. (2017). "Genetics and genomics of ovarian sex cord-stromal tumors". Clinical Genetics. 91 (2): 285–291. doi:10.1111/cge.12917. ISSN 0009-9163.
- ↑ "onlinelibrary.wiley.com".