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The above is not applied clinically. A panel of [[immunostains]] (ER, PR, HER2, EGFR, CK5/6) can reproduce the molecular groupings | The above is not applied clinically. A panel of [[immunostains]] (ER, PR, HER2, EGFR, CK5/6) can reproduce the molecular groupings; however, these groupings originate from gene expression profiling studies<ref name=pmid19704256>{{Cite journal | last1 = Tang | first1 = P. | last2 = Skinner | first2 = KA. | last3 = Hicks | first3 = DG. | title = Molecular classification of breast carcinomas by immunohistochemical analysis: are we ready? | journal = Diagn Mol Pathol | volume = 18 | issue = 3 | pages = 125-32 | month = Sep | year = 2009 | doi = 10.1097/PDM.0b013e31818d107b | PMID = 19704256 }}</ref> | ||
Basal-like breast cancer | Basal-like breast cancer | ||
*Overview | *Overview | ||
**A type of breast cancer | **A type of breast cancer defined by gene expression profiling | ||
**Can be identified by expression of basal markers (CK14, p63, calponin, SMA) | |||
**Not derived from myoepithelial cells, merely express a phenotype more in keeping with basal cells than ductal cells | **Not derived from myoepithelial cells, merely express a phenotype more in keeping with basal cells than ductal cells | ||
**Most triple negative (ER, PgR, Her-2); therefore cannot be treated with the usual therapeutic agents | **Most triple negative (ER, PgR, Her-2); therefore cannot be treated with the usual therapeutic agents | ||
**There is an association in young women between basal-like breast cancer and BRCA mutation | **There is an association in young women between basal-like breast cancer and BRCA mutation. | ||
**Sporadic basal-like cancers do not have a BRCA mutation but may have a dysfunctional BRCA1 pathway. | |||
*Classic | *This molecular group includes a variety of morphologic phenotypes including: | ||
**High grade invasive ductal mammary carcinoma of no special type. | |||
**Medullary-like mammary carcinoma (a carcinoma with some but not all the features of medullary carcinoma). | |||
**Medullary mammary carcinomas | |||
**Metaplastic mammary carcinomas | |||
**Mammary adenoid cystic carcinoma | |||
**Secretory mammary carcinoma | |||
*Classic morphological clues of a basal type cancer usually refer to medullary carcinoma features: | |||
**Relatively circumscribed | **Relatively circumscribed | ||
**Geographic necrosis | **Geographic necrosis | ||
**Abundant mitoses | **Abundant mitoses | ||
**Pushing margins | |||
* | **Central fibrosis or necrosis | ||
** | **High histological grade | ||
** | **Exceptionally high mitotic rate | ||
** | **Pushing borders | ||
** | **Conspicuous lymphocytic infiltrate | ||
*Behaviour | *Behaviour | ||
**Basal-like breast cancer is a heterogeneous group | **Basal-like breast cancer is a heterogeneous group. | ||
**The behaviour of basal-like breast cancer appears to fall into two groups: | **The behaviour of basal-like breast cancer appears to fall into two groups: | ||
***The tumours that do not metastasise have a better prognosis than other grade 3 IDC | ***The tumours that do not metastasise have a better prognosis than other grade 3 IDC | ||
***Tumours with early metastasis | ***Tumours with early metastasis | ||
****Hematogenous spread -greater tendency to metastasise to visceral sites associated with poorer prognosis (such as lung and brain) instead of to nodes and bone | |||
Triple Negative Breast Carcinomas | Triple Negative Breast Carcinomas | ||
**Triple-negative and basal-like phenotypes are not synonymous but overlap | **About 15% of breast carcinomas. | ||
** | **Important group due to a lack of tailored therapies for this group | ||
**Triple-negative and basal-like phenotypes are not synonymous but overlap | |||
***About 70% of triple-negative tumours are basal-like. | |||
***About 70% of basal-like tumors are triple-negative tumours are. | |||
**Classic morphological clues of a basal type cancer usually refer to medullary carcinoma features. | |||
==Immunostains for typing and diagnosis== | ==Immunostains for typing and diagnosis== |
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