Tag Archives: hnpcc

Hereditary Non-Polyposis Colorectal Cancer Syndrome

Hereditary Non-Polyposis Colorectal Cancer Syndrome

Clinical: earlier onset of cancer , ~ 45 years

Genetics:
- mutation in DNA mismatch repair genes: hMLH1, hMSH2,

hPMS1/2
- results in MSI (expansion or contraction)
- microsatellite: tandem repeats of 1-4 nucleotides

Extracolonic lesions:

Cholangiocarcinoma
Endometrial carcinoma
Ovarian cancer

Amsterdam and Bethesda criteria:
- family history of colorectal cancer
- previous relative with colorectal cancer less than 50 years

Histology

- more likely to have right-sided colonic lesions
- more poorly differentiated
- lymphocytic infiltration
- mucinous differentiation
- no dirty necrosis

Immunohistochemistry

- hMLH1, hMSH2  loss of staining suggests mutation in gene with additional DNA testing for MSI expansion, contraction

Posted in Colon | Tagged , , , , , , , , , , , | Comments Off

Endometrial Cancer Risk Factors

Endometrial Cancer Risk Factors

Uterine Cancer Risk Factors

1.    Obesity

2.    Hypertension

3.    Diabetes

4.    Infertility (nulliparous, functional menstrual abnormalities with anovulatory cycles)

5.    Unopposed estrogen therapy

6.    Early menarche, late menopause

7.    Family history (HNPCC-related)

8.    Estrogen-secreting tumours (eg. granulosa cell tumor)

Posted in Uterus | Tagged , , , , , | Comments Off

Colon Cancer Risk Factors

Colon Cancer Risk Factors

Risk factors with high incidence

-age
-Ulcerative Colitis
-Crohn’s Disease
-FAP
-HNPCC

Posted in Colon | Tagged , , , , , , , | Comments Off

Hereditary Nonpolyposis Colorectal Cancer Syndrome


Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Syndrome

 

Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Syndrome, also known as Lynch syndrome, is a rare colorectal syndrome that can lead to cancer of the colon.

Hereditary Nonpolyposis Colorectal Cancer Syndrome Inheritance pattern
- autosomal dominant
- syndromal patients have only one functional allele and cancer occurs through loss of heterozygosity (LOH)
- mutations occur in mismatch repair genes (MLH1, MSH 2, MSH6, PMS 1, PMS 2)
- mutations lead to microsatellite instability which are mostly repeats in intronic regions

What to look for?

- you can look for the loss of the genes themselves

- you can look at particular microsatellite loci and see how many have instability
- 0/5 – stable
- 1/5 – low frequency instability
- 2 or greater/5  – high frequency of instability – MSI-H
- microsatellite instability is NOT specific to HNPCC, as it is seen in 10-15 % of sporadic colorectal carcinomas. Sporadic tumors arise in older patients who lack a family history. The activity of the mismatch repair genes in sporadic tumors is lost through hypermethylation

Diagnostic criteria is through the Amsterdam II criteria

Clinical presentation

- development of multiple cancers at an early age, including cancer of the colon, endometrium, renal pelvis and ureter, small bowel, ovary, brain, hepatobiliary tract and sebaceous tumors 

Muir -Torre Syndrome

- sebaceous tumors along with HNPCC type of internal malignancy

Turcot Syndrome

- tumors of the CNS (usually gliobalstomas) and multiple colorectal tumors

Gross Appearance

- predilection for right colon and cecum all the way to the transverse colon
- usually polypoid in appearnace rather than diffuse

 

Microscopic Appearance

- sporadic tumors have the same features as tumors associated with HNPCC

- proximally located mucinous type of colorectal adenocarcinomas +/- tumor infiltrating lymphocytes

- proximally located, poorly differentiated medullary or undifferentiated colorectal adenocarcinomas – these are well circumscribed and lacking abundant desmoplastic stroma and may contain tumor infiltrating lymphocytes

- adenomas – many have a villous morphology and high grade dysplasia, with rapid progression to carcinoma

Posted in Colon, GI, Syndrome | Tagged , , , , , , , , , , , , , , , , , | Leave a comment