Thursday, October 18, 2012

Blood in Stool


Bleeding from the bowel is an important symptom that should always be checked out by a doctor.
At the age of 28 it is not likely to be anything serious, but it still needs to be diagnosed accurately and I think that you should see your GP to consider further examination.
I cannot give you a diagnosis, but I can offer some background information that I hope will be of some help.
More often than not there is an entirely harmless explanation for bleeding from the bowel, but most folk need some perspective and reassurance about the possibility of bowel cancer.
The overall lifetime risk of developing bowel cancer by the age of 80 years is about 4 per cent across the population and the great majority of these occur in people over the age of 45 years.
Under the age of 45 bowel cancer is very rare, unless it runs in the family.
A significant family history is one that contains a first degree relative (brother, sister, parent or child) under the age of 55 affected by cancer of the bowel or womb, or more than one such relative affected at any age.
A blood-stained stool is most likely to result from bleeding in your anal canal. The usual culprits are haemorrhoids (piles) that are capable of quite profuse blood loss or a small crack in the skin of the anus (a fissure).
Inflamed bowel can bleed too, but generally speaking it causes other symptoms as well, such as colic (spasmodic pain like trapped wind), diarrhoea or mucus (clear or blood-stained jelly).
Inflamed bowel can result from ulcerative colitisCrohn's disease (chronic inflammation of the intestine), or rare intestinal infections that are associated with prolonged antibiotic treatment or travel to exotic locations.
You might have read that Mefenamic acid can be associated with internal bleeding.
Like all anti-inflammatory painkillers it can cause irritation of the lining of the stomach in some people and in the most unlucky cases, ulceration and bleeding from the upper gut.
Such bleeding tends to present with partially digested blood in the stool (melaena) which is very black and tarry.
It's quite different from the normal motion and is suggestive of a significant internal bleed. Melaena represents a medical emergency and justifies urgent consultation.
Assuming that you don't have a family history like the one described, or any of the other symptoms that I've mentioned, it is most likely that you are bleeding from your anal canal.
However, I think most clinicians would agree that you'd be wise to get examined by your doctor, who may recommend that you have the lower part of your bowel investigated by a specialist.
Yours sincerely
The NetDoctor Medical Team
Source:

Anal Cancer


The anus is the name for the muscular opening at the very end of the large bowel.

It is controlled by a ring of muscle called a sphincter that opens and closes to control bowel movements. The area that connects the anus to the rectum is called the anal canal and is around 3–4cm (1–1½in) long (see diagram below).

Cancer of the anus is rare. Around 930 people are diagnosed with anal cancer each year in the UK.

The most common type of anal cancer is squamous cell carcinoma. Other rarer types are basal cell carcinoma, adenocarcinoma and melanoma. This information is about squamous cell carcinoma.



Causes and possible risk factors

Anal cancer is slightly more common in women than men. There are a number of factors that can increase your risk of developing anal cancer. These include:

Human papilloma virus (HPV)
Anal cancer is more likely to develop in people who have had a viral infection called thehuman papilloma virus (HPV). The risk of having HPV increases with the number of sexual partners you have.

Sexual activity
People who have anal intercourse are more likely to develop anal cancer. This may be because they are more likely to have anal HPV.

Lowered immunity
The immune system is part of the body's defence against infections and illnesses like cancer.

Anal cancer is more common in people who have a lowered immunity, such as people taking medicines to suppress their immune system after an organ transplant or people with conditions such as HIV.

Smoking
Smoking tobacco increases the risk of developing anal cancer. We have more information on stopping smoking.

However, many people who get anal cancer will not have these risk factors and the cause remains unknown.

Genetic - Prostate Cancer Risk

Genetic background may contribute to prostate cancer risk, as suggested by associations with race, family, and specific gene variants. Men who have a first-degree relative (father or brother) with prostate cancer have twice the risk of developing prostate cancer, and those with two first-degree relatives affected have a fivefold greater risk compared with men with no family history.[18] In the United States, prostate cancer more commonly affects black men than white or Hispanic men, and is also more deadly in black men.[19] [20] In contrast, the incidence and mortality rates for Hispanic men are one third lower than for non-Hispanic whites. Studies of twins in Scandinavia suggest that forty percent of prostate cancer risk can be explained by inherited factors.[21

No single gene is responsible for prostate cancer; many different genes have been implicated. Mutations in BRCA1 and BRCA2, important risk factors for ovarian cancer and breast cancer in women, have also been implicated in prostate cancer.[22] Other linked genes include the Hereditary Prostate cancer gene 1 (HPC1), the androgen receptor, and the vitamin D receptor.[19] TMPRSS2-ETS gene family fusion, specifically TMPRSS2-ERG or TMPRSS2-ETV1/4 promotes cancer cell growth.[23]

Loss of cancer suppressor genes, early in the prostatic carcinogenesis, have been localized to chromosomes 8p, 10q, 13q,and 16q. P53 mutations in the primary prostate cancer are relatively low and are more frequently seen in metastatic settings, hence, p53 mutations are late event in pathology of prostate cancer. Other tumor suppressor genes that are thought to play a role in prostate cancer include PTEN (gene) and KAI1. "Up to 70 percent of men with prostate cancer have lost one copy of the PTEN gene at the time of diagnosis"[24] Relative frequency of loss of E-cadherin and CD44 has also been observed.

Prostate Cancer Staging


Prostate cancer staging is the process by which physicians categorize the risk of cancer having spread beyond the prostate, or equivalently, the probability of being cured with local therapies such as surgery or radiation. Once patients are placed in prognostic categories, this information can contribute to the selection of an optimal approach to treatment. The information considered in such a prognostic classification can be based on physical examination, imaging studies and blood tests (so-called "clinical stage"), or based on the extent of disease as revealed in a surgical specimen (so-called "pathologic stage").
There are two schemes commonly used to stage prostate cancer. The most common is promulgated by the American Joint Committee on Cancer, and is known as the TNM system, which evaluates the size of the tumor, the extent of involved lymph nodes, and any metastasis (distant spread) and also takes into account cancer grade. As with many other cancers, these are often grouped into four stages (I–IV). Another scheme, now used less commonly for research, but often still used by clinicians,[citation needed] is the Whitmore-Jewett stage.[1]
Briefly, Stage I disease is cancer that is found incidentally in a small part of the sample when prostate tissue was removed for other reasons, such as benign prostatic hypertrophy, and the cells closely resemble normal cells and the gland feels normal to the examining finger. In Stage II more of the prostate is involved and a lump can be felt within the gland. In Stage III, the tumor has spread through the prostatic capsule and the lump can be felt on the surface of the gland. In Stage IV disease, the tumor has invaded nearby structures, or has spread to lymph nodes or other organs. The Gleason Grading System is based on cellular content and tissue architecture from biopsies, which provides an estimate of the destructive potential and ultimate prognosis of the disease.

Prostate Cancer

What Are Colon Cancer Symptoms?


Getting a Handle on Colon Cancer Symptoms

Colon cancer symptoms aren't always obvious, but you can learn what these symptoms look and feel like. Understanding colon cancer symptoms is important, because you can use this knowledge to work with your doctor to find out the cause and take care of your long-term health.

What is the Colon?

In order to understand what colon cancer symptoms might feel like, it helps to learn a bit about the colon. The colon is an important part of the digestive system, and as such, it has a major role in helping the body absorb nutrients, minerals, and water. The colon also helps rid the body of waste in the form of stool. The colon makes up the majority of the large intestine, approximately six feet in length. The last six inches or so of the large intestine are the rectum and the anal canal.

What are the Symptoms of Colon Cancer?

Colon cancer can have many symptoms. However, in the early stages, people with colon cancer often have no symptoms at all. This is why regular screening beginning at 50 is an important investment in your healthy future.
Colon cancer symptoms come in two general varieties:
  1. Local
  2. Systemic

Local Colon Cancer Symptoms

Local colon cancer symptoms affect your bathroom habits and the colon itself. Some of the more common local symptoms of colon cancer include:
If you experience any of these for two or more weeks, call your doctor right away to discuss your concerns and arrange for tests to get to the bottom of your symptoms.

Systemic Colon Cancer Symptoms

Systemic colon cancer symptoms are those that affect your whole body, such as weight loss, and include:
  • Unintentional weight loss (losing weight when not dieting or trying to lose weight)
  • Loss of appetite
  • Unexplained fatigue (extreme tiredness)
  • Nausea or vomiting
  • Anemia (low red blood cell count or low iron in your red blood cells)
  • Jaundice (yellow color to the skin and whites of the eyes)
If you experience any of these for any length of time, even a few days, call your doctor right away to discuss your concerns and arrange for tests to get to the bottom of your symptoms.

What Should I Do if I Have Colon Cancer Symptoms?

Call your doctor so he or she can set up an appointment to see you. During the appointment your doctor will take a medical history, collect blood samples for testing, and schedule you for follow-up tests, if needed.
Many people are afraid of colon cancer screening. They worry that it will hurt and that it is embarrassing. Your doctor and nurse have performed hundreds, and in some cases even thousands, of these procedures. There is nothing to be embarrassed about and remember: Even your doctor and nurse undergo these same tests to take care of their own health.

Preparing for Colon Cancer Tests

If you are worried about preparing for your colon cancer tests, ask your doctor about how best to get ready for any procedures. There are different medications for clearing your colon of stool to ensure a good screening. There is no reason to suffer in silence!
Diagnosis of Colon Cancer and How Not to Dread Colon Cancer Screening provide detailed information on screening procedures, plus tips on how to make preparing for these tests easier.
Sources
The American Cancer Society: Learn about Colon and Rectum Cancer. Accessed: January 20, 2009.
http://www.cancer.org/docroot/CRI/CRI_2x.asp?sitearea=&dt=10
The Colon Cancer Alliance. Accessed: January 20, 2009.
http://www.ccalliance.org
The Colorectal Cancer Coalition. Accessed: January 20, 2009.
http://www.fightcolorectalcancer.org
The Colon Cancer Foundation. Accessed: January 20, 2009.
http://www.coloncancerfoundation.org
The National Cancer Institute: Colon and Rectal Cancer. Accessed: January 20, 2009.
http://www.cancer.gov/cancertopics/types/colon-and-rectal


Source:

Cancer During Pregnancy

Cancer during pregnancy is rare, occurring in approximately one out of every 1,000 pregnancies, and little research is available to guide women and doctors. However, a pregnant woman with cancer is capable of giving birth to a healthy baby, and some cancer treatments are safe during pregnancy. Cancer rarely affects the fetus directly. Although some cancers may spread to the placenta (a temporary organ that connects the mother and fetus), most cancers cannot spread to the fetus itself.
The cancers that tend to occur during pregnancy are those that are more common in younger people, such as cervical cancerbreast cancerthyroid cancerHodgkin lymphoma, and melanoma. In addition, a gestational trophoblastic tumor is a rare cancer that occurs in a woman's reproductive system. It is most commonly the result of an abnormal combination of a sperm and an egg; in other cases, it begins from a normal placenta.
Because age is the most significant risk factor for cancer, the rate of cancer during pregnancy may be increasing as more women are waiting until they are older to have children.
Diagnosis
Being pregnant often delays a cancer diagnosis because some cancer symptoms such as abdominal bloating, frequent headaches, or rectal bleeding are common during pregnancy and are not considered suspicious.
Breast cancer is the most common cancer in pregnant women, affecting approximately one in 3,000 pregnancies. Pregnancy-related breast enlargement may make it difficult to detect small breast tumors, and mammograms are not regularly done during pregnancy.
If cancer is suspected during pregnancy, women and their doctors may be concerned about diagnostic tests such as x-rays. However, research has shown that the level of radiation in diagnostic x-rays is too low to harm the fetus. When possible, women may use a lead shield that covers the abdomen for extra protection. Other diagnostic tests—such as magnetic resonance imaging (MRI)ultrasound, andbiopsy—are also considered safe during pregnancy because they don't use ionizing radiation.
Sometimes, pregnancy can uncover cancer that had previously gone undetected. For example, a Pap test performed as part of standard prenatal care can detect cervical cancer. Similarly, an ultrasound performed during pregnancy can find ovarian cancer that might otherwise go undiagnosed.
Treatment
When making treatment decisions for cancer during pregnancy, the doctor considers the best treatment options for the mother and the possible risks to the fetus. The type of treatment given depends on many factors, including gestational age of the fetus (stage of the pregnancy); the type, location, size, and stage of the cancer; and the wishes of the expectant mother and family. Because some cancer treatments can harm the fetus, especially during the first trimester (the first three months of pregnancy), treatment may be delayed until the second or third trimesters. When cancer is diagnosed later in pregnancy, doctors may wait to start treatment until after the baby is born, or they may consider inducing labor early. In some cases, such as early-stage (stage 0 or IA) cervical cancer, doctors may wait to treat the cancer until after delivery.
Some cancer treatments may be used during pregnancy but only after careful consideration and treatment planning to optimize the safety of the mother and the unborn baby. These include surgery, chemotherapy, and rarely, radiation therapy.
Surgery. Surgery is the removal of the tumor and surrounding tissue during an operation. It poses little risk to the fetus and is considered the safest cancer treatment option during pregnancy. In some instances, more extensive surgery can be done to avoid having to use chemotherapy or radiation therapy.
Chemotherapy. Chemotherapy is the use of drugs to kill cancer cells, usually by stopping the cancer cells' ability to grow and divide. Chemotherapy can harm the fetus, particularly if it is given during the first trimester of pregnancy when the fetus' organs are still developing. Chemotherapy during the first trimester may cause birth defects or even the loss of the unborn baby. During the second and third trimesters, some types of chemotherapy may be given without necessarily harming the fetus. The placenta acts as a barrier between the mother and the fetus, and some drugs cannot pass through the barrier, or they pass through only minimally. If the planned chemotherapy includes a drug that is not safe during any stage of pregnancy, the doctor can sometimes substitute another drug. Although chemotherapy in the later stages of pregnancy may not directly harm the fetus, it may cause side effects—such as malnutrition and anemia, meaning a low read blood cell count—for the mother that may indirectly harm the fetus. In addition, chemotherapy given during the second and third trimesters often causes early labor and low birth weight, both of which may lead to further health concerns for the mother and the baby. The baby may struggle to gain weight and fight infections, and the mother may have trouble breastfeeding.?
Radiation therapy. Radiation therapy is the use of high-energy x-rays or other particles to kill cancer cells. Because radiation therapy can harm the fetus, particularly during the first trimester, doctors generally avoid using this treatment. Even in the second and third trimesters, the use of radiation therapy is rare, and it depends on the dose of radiation and the area of the body being treated. 
Breastfeeding
Although cancer cells cannot pass to the infant through breast milk, doctors advise women who are being treated for cancer not to breastfeed. Chemotherapy can be especially dangerous because the drugs may be transferred to the infant through the breast milk, causing harm. Similarly, radioactive components that are taken internally, such as radioactive iodine used in treating thyroid cancer, also cross into breast milk and can harm the infant.
How pregnancy affects chance of recovery from cancer
The prognosis (chance of recovery) for a pregnant woman with cancer is often the same, compared with other women of the same age with the same type and stage of cancer. However, if a woman's diagnosis is delayed during pregnancy, the extent of the cancer at the time of diagnosis may be greater, resulting in a worse overall prognosis. In addition, pregnancy sometimes affects the behavior of some cancers. For example, there is some evidence to suggest that the hormonal changes of pregnancy may stimulate the growth of malignant melanoma.
Pregnancy after cancer treatment
As more young people are surviving cancer, more women are considering whether they should have a baby after having cancer. In general, pregnancy after cancer treatment is considered safe for both the mother and the baby, and pregnancy does not appear to increase the chances of cancer recurring (coming back). However, because some cancers do recur, women are usually advised to wait a number of years after completing cancer treatment until the risk of recurrence has decreased. The amount of time a patient may be advised to wait before trying to become pregnant depends on the type and stage of cancer, the type of treatment the patient received, and the patient's preferences.
Sometimes, cancer treatments can damage specific areas of the body, such as the heart or lungs. Before becoming pregnant, your doctor may need to evaluate these organs to be sure that the pregnancy will be safe.
Unfortunately, some cancer treatments also cause infertility, making it difficult or impossible for some women to have children. All women of childbearing age who are interested in having children in the future should talk with their doctor about treatment-related infertility risks and fertility preservation strategies before beginning treatment. 

Read ASCO's guideline on fertility preservation and cancer treatment to learn about options to preserve fertility before cancer treatment.