Tagged with “Lynch syndrome”

Is Breast Cancer Linked to Lynch Syndrome?

Although breast cancer has not traditionally been considered one of the cancers associated with Lynch syndrome, evidence is building that there might be a link.

Breast cancer may actually be with in the spectrum of Lynch cancers.

An Australian team reviewing the pathology of breast cancers in women who carried a mutation for Lynch syndrome ( hereditary non-polyposis colon cancer) found that half of the breast tumors were mismatch repair deficient — a hallmark of Lynch cancers. Continue reading…

Posted by Kate Murphy on July 30th, 2010
Posted in: Research & Treatment News | 2 Comments »
Tags: breast cancer, Lynch syndrome

Annual Colonoscopy for Lynch Syndrome

Annual colonoscopies for people with Lynch syndrome (HNPCC or hereditary nonpolyposis colon cancer) successfully find cancers at an early stage.

A recent study by the German HNPCC Consortium confirmed the effectiveness of annual colonoscopies to find colorectal cancers at a curable stage. Regular colonoscopies found early cancers more often than did patient symptoms.

Current recommendations are for surveillance colonoscopies to begin by age 25, be repeated every 1 to 2 years until age 40, and then annually.

Posted by Kate Murphy on March 12th, 2010
Posted in: Research & Treatment News | No Comments »
Tags: colonoscopy, HNPCC, Lynch syndrome

Choosing the Best Colon Surgery for Lynch Syndrome

Removing the entire colon (subtotal colectomy) is sometimes recommended for patients with Lynch syndrome when colon cancer is diagnosed. In addition, some people who have an inherited Lynch mutation have their colons removed to prevent colon cancer.

While subtotal colectomy didn’t reduce deaths from Lynch-related colon cancer, it did cut down on additional colorectal cancer diagnoses and the need for other abdominal surgery. Continue reading…

Posted by Kate Murphy on February 5th, 2010
Posted in: Research & Treatment News | No Comments »
Tags: Lynch syndrome, subtotal colectomy, surgery

Risk for Lynch Syndrome Related Cancers in MSH6 Mutations

People with a mutation in the MSH6 gene, part of the Lynch syndrome, have a greatly increased risk of colorectal, endometrial, and other related cancers. The cancers can occur in old age, with an increasing risk from age 70 to 80.

About 4 in every 1000 colorectal cancers are due to an inherited mutation in the MSH6 gene. It accounts for about 10 to 20 percent of Lynch syndrome mutations.

By the time they are 80 years old, men have eight times the risk of getting colorectal cancer and women have 26 times the risk of endometrial cancer — cancer that begins in the lining of the uterus.

Posted by Kate Murphy on December 23rd, 2009
Posted in: Research & Treatment News | No Comments »
Tags: inherited cancer, Lynch syndrome, MSH6