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endometrial endometrioid adenocarcinoma

Tuesday 6 January 2004

Endometrioid carcinoma of the uterus; type 1 endometrial carcinoma

PO

Definition: Relatively indolent tumors that arise in background of endometrial hyperplasia.

Images

- Endometrioid adenocarcinoma with squamous metaplasia

Immunochemistry

- p53

  • Uterine papillary serous adenocarcinomas (UPSA) showed significantly higher p53 expression than did uterine endometrioid adenocarcinomas (UEA) (76.2% versus 35%), whereas both ER and PR are more often positive in endometrioid than in serous tumors.
  • In endometrioid carcinoma, p53 overexpression is associated with high-grade and advanced-stage tumors (p =.0006 and.006), whereas ER and PR expression is associated with low-grade and early-stage tumors (p =.0006 and.0001; p =.003 and.0006).

- BCL2
* No significant difference was found in bcl-2 and bax expression between both histologic types. However, there is definite decrease in intensity of bcl-2 in UPSA compared with UEA.

  • Bcl-2 immunopositivity is more common in low-grade, early-stage rather than in high-grade, advanced-stage adenocarcinomas, but the difference was not statistically significant (p =.24 and.07).

- BAX

  • Bax immunopositivity is associated with well-differentiated (p =.04) and early-stage tumors. Furthermore, a significant inverse relationship between bax and p53 reactivity is defined (p =.05), especially in tumors of endometrioid type.
  • Bax and PR immunoexpression correlated near the limit of statistical significance (p =.08), whereas no relationship was found among bax, bcl-2, and ER immunopositivity.

The differences in immunohistochemical profiles of endometrioid and serous carcinomas support the existence of different molecular pathways of their development.

(http://www.nature.com/modpathol/journal/v13/n4/full/3880062a.html)

Differential diagnosis

- Ciliary metaplasia
- Papillary change
- Progesterone treatment related changes
- Shedding endometrium with papillary syncytial metaplasia
- Villoglandular endometrioid carcinoma
- Well differentiated tumors: atypical hyperplasia / EIN (Mod Pathol 2000;13:309)
- Poorly differentiated tumors: serous carcinoma

Reporting

- Dilemmas in Reporting of Endometrial Carcinomas http://www.pathsoc.org/files/meetings/edinburghpreswed/0940%20Weds%20Fintry%20McCluggage%201%20of%202.pdf

Comparative genomic hybridization (CGH)

- CGH gains

  • 1q25-q42 gains (30%)
  • 19pter-p13.1 (26%)
  • 19q13.1-q13.3 (19%).
  • 8q21—qter (17%)
  • 10q21—>q23 (14%)
  • 10p (13%)

- CGH losses

  • 4q22-qter losses (8%)
  • 16q21-qter losses (8%)
  • 18q21-qter losses (8%)

See also

- endometrial tumors
- endometrioid adenocarcinomas
- Tumors
- Oncobase
- Oncogen

References

- Levan K, Partheen K, Osterberg L, Helou K, Horvath G. Chromosomal alterations in 98 endometrioid adenocarcinomas analyzed with comparative genomic hybridization. Cytogenet Genome Res. 2006;115(1):16-22. PMID: 16974079