Difference between revisions of "Breast Cancer"

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'''Breast Cancer'''
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This page is under construction
  
−
This page is under construction
 
 
We need your help!  
 
We need your help!  
 +
 
Please consider joining in the project and submitting a review
 
Please consider joining in the project and submitting a review
  
 
'''Contents'''
 
'''Contents'''
 +
 
1 Primary Author(s)*
 
1 Primary Author(s)*
 +
 
2      Graphical Data
 
2      Graphical Data
 +
 
2 General Disease Overview / Description of Cancer Category
 
2 General Disease Overview / Description of Cancer Category
 +
 
3 WHO Classification Pages (Includes Links to Content)
 
3 WHO Classification Pages (Includes Links to Content)
 +
 
4 Other Related Pages (Includes Links to Content)
 
4 Other Related Pages (Includes Links to Content)
 +
 
5 Additional Information
 
5 Additional Information
 
6 References
 
6 References
 +
 
6.1 EXAMPLE Book
 
6.1 EXAMPLE Book
 +
 
6.2 EXAMPLE Journal Article
 
6.2 EXAMPLE Journal Article
 +
 
7 Notes
 
7 Notes
  
 
'''Primary Author(s)*'''
 
'''Primary Author(s)*'''
 +
 
Put your text here
 
Put your text here
  
  
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'''Graphical Data''' Links[edit | edit source]
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'''Graphical Data''' '''Links'''
 +
 
 +
[edit | edit source]
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'''Table 5: Genes with known hereditary risk associations in breast cancer according to National Comprehensive Cancer Network (NCCN) Guidelines (version 3.2019)'''
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{| class="wikitable"
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|'''Gene'''
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|'''Associated  Syndrome; Breast Cancer Subtype'''
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|-
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|''ATM''
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|Ataxia  telangiectasia syndrome
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|-
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|''BRCA1''
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|BRCA-Related  Breast/ Ovarian Cancer Syndrome; TNBC
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|-
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|''BRCA2''
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|BRCA-Related  Breast/ Ovarian Cancer Syndrome; TNBC
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|-
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|''CDH1''
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|Hereditary  Diffuse Gastric Cancer and Lobular Breast Cancer
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|-
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|''CHEK2''
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|Inherited  breast cancer
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|-
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|''NBN''
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|Nijmegen  Breakage Syndrome (autosomal recessive inheritance)
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|-
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|''NF1''
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|Neurofibromatosis  type 1
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|-
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|''PALB2''
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|Fanconi  anemia
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|-
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|''PTEN''
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|Cowden  syndrome
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|-
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|''STK11''
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|Peutz-Jeghers  syndrome
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|-
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|''TP53''
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|Li-Fraumeni  syndrome
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|}
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Inheritance is autosomal dominant with incomplete penetrance, unless otherwise specified
 +
 
 +
'''General Disease Overview / Description of Cancer Category'''
  
−
'''General Disease Overview''' / Description of Cancer Category
 
 
Put your text here
 
Put your text here
  
−
'''WHO Classification Pages''' (Includes Links to Content)
+
'''WHO Classification Pages'''  
 +
 
 +
(Includes Links to Content)
 +
 
 
Put your text here, EXAMPLE #Chromophobe renal cell carcinoma
 
Put your text here, EXAMPLE #Chromophobe renal cell carcinoma
  
−
'''Other Related Pages''' (Includes Links to Content)
+
'''Other Related Pages'''  
 +
 
 +
(Includes Links to Content)
 +
 
 
Put your text here, EXAMPLE #Acute Myeloid Leukemia (AML) with Mutated FLT3
 
Put your text here, EXAMPLE #Acute Myeloid Leukemia (AML) with Mutated FLT3
  
 
Additional Information
 
Additional Information
 +
 
Put your text here
 
Put your text here
  
 
'''References'''
 
'''References'''
 +
 
EXAMPLE Book
 
EXAMPLE Book
 
Arber DA, et al., (2008). Acute myeloid leukaemia with recurrent genetic abnormalities, in World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th edition. Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J, Vardiman JW, Editors. IARC Press: Lyon, France, p117-118.
 
Arber DA, et al., (2008). Acute myeloid leukaemia with recurrent genetic abnormalities, in World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th edition. Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J, Vardiman JW, Editors. IARC Press: Lyon, France, p117-118.
 +
 
EXAMPLE Journal Article
 
EXAMPLE Journal Article
 
Li Y, et al., (2001). Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia. Nat Genet 28:220-221, PMID 11431691.
 
Li Y, et al., (2001). Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia. Nat Genet 28:220-221, PMID 11431691.
  
 
'''Notes'''
 
'''Notes'''
 +
 
*Primary authors will typically be those that initially create and complete the content of a page. If a subsequent user modifies the content and feels the effort put forth is of high enough significance to warrant listing in the authorship section, please contact the CCGA coordinators (contact information provided on the homepage). Additional global feedback or concerns are also welcome.
 
*Primary authors will typically be those that initially create and complete the content of a page. If a subsequent user modifies the content and feels the effort put forth is of high enough significance to warrant listing in the authorship section, please contact the CCGA coordinators (contact information provided on the homepage). Additional global feedback or concerns are also welcome.
  
 
Category: Pages using PMID magic links
 
Category: Pages using PMID magic links

Latest revision as of 16:45, 11 July 2019

This page is under construction

We need your help!

Please consider joining in the project and submitting a review

Contents

1 Primary Author(s)*

2 Graphical Data

2 General Disease Overview / Description of Cancer Category

3 WHO Classification Pages (Includes Links to Content)

4 Other Related Pages (Includes Links to Content)

5 Additional Information 6 References

6.1 EXAMPLE Book

6.2 EXAMPLE Journal Article

7 Notes

Primary Author(s)*

Put your text here


Graphical Data Links

[edit | edit source]

Table 5: Genes with known hereditary risk associations in breast cancer according to National Comprehensive Cancer Network (NCCN) Guidelines (version 3.2019)

Gene Associated Syndrome; Breast Cancer Subtype
ATM Ataxia telangiectasia syndrome
BRCA1 BRCA-Related Breast/ Ovarian Cancer Syndrome; TNBC
BRCA2 BRCA-Related Breast/ Ovarian Cancer Syndrome; TNBC
CDH1 Hereditary Diffuse Gastric Cancer and Lobular Breast Cancer
CHEK2 Inherited breast cancer
NBN Nijmegen Breakage Syndrome (autosomal recessive inheritance)
NF1 Neurofibromatosis type 1
PALB2 Fanconi anemia
PTEN Cowden syndrome
STK11 Peutz-Jeghers syndrome
TP53 Li-Fraumeni syndrome

Inheritance is autosomal dominant with incomplete penetrance, unless otherwise specified

General Disease Overview / Description of Cancer Category

Put your text here

WHO Classification Pages

(Includes Links to Content)

Put your text here, EXAMPLE #Chromophobe renal cell carcinoma

Other Related Pages

(Includes Links to Content)

Put your text here, EXAMPLE #Acute Myeloid Leukemia (AML) with Mutated FLT3

Additional Information

Put your text here

References

EXAMPLE Book Arber DA, et al., (2008). Acute myeloid leukaemia with recurrent genetic abnormalities, in World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th edition. Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J, Vardiman JW, Editors. IARC Press: Lyon, France, p117-118.

EXAMPLE Journal Article Li Y, et al., (2001). Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia. Nat Genet 28:220-221, PMID 11431691.

Notes

  • Primary authors will typically be those that initially create and complete the content of a page. If a subsequent user modifies the content and feels the effort put forth is of high enough significance to warrant listing in the authorship section, please contact the CCGA coordinators (contact information provided on the homepage). Additional global feedback or concerns are also welcome.

Category: Pages using PMID magic links

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