Thursday, November 12, 2015

Signs and symptoms of liver cancer often do not show up until the later stages of the disease, but sometimes they may show up sooner. If you go to your doctor when you first notice symptoms, your cancer might be diagnosed earlier, when treatment is most likely to be helpful. Some of the most common symptoms of liver cancer are:


                                         





    #Weight loss (without trying)

    #Loss of appetite

    #Feeling very full after a small meal

    #Nausea or vomiting

    #An enlarged liver, felt as a mass under the ribs on the right side

    #An enlarged spleen, felt as a mass under the ribs on the left side

    #Pain in the abdomen or near the right shoulder blade

    #Swelling or fluid build-up in the abdomen

    #Itching

    #Yellowing of the skin and eyes (jaundice)

Some other symptoms can include fever, enlarged veins on the belly that can be seen through the skin, and abnormal bruising or bleeding.

People who have chronic hepatitis or cirrhosis may feel worse than usual or just have changes in lab test results, such as alpha-fetoprotein (AFP) levels.

Some liver tumors make hormones that act on organs other than the liver. These hormones may cause:

    #High blood calcium levels (hypercalcemia), which can cause nausea, confusion, constipation, weakness, or muscle problems

    #Low blood sugar levels (hypoglycemia), which can cause fatigue or fainting

    #Breast enlargement (gynecomastia) and/or shrinkage of the testicles in men

    #High counts of red blood cells (erythrocytosis) which can cause someone to look red and flushed
    High cholesterol levels

Many of the signs and symptoms of liver cancer can also be caused by other conditions, including other liver problems. Still, if you have any of these problems, it's important to see your doctor right away so the cause can be found and treated, if needed.

Source By.....http://www.cancer.org/cancer/livercancer/detailedguide/liver-cancer-signs-symptoms

Wednesday, November 11, 2015

 

causes eye cancer


The exact cause of most eye cancers is not known. But scientists have found that the disease is linked with some other conditions, which are described in the section “What are the risk factors for eye cancer?” A great deal of research is being done to learn more about the causes.

Scientists are learning how certain changes in the DNA inside cells can cause the cells to become cancerous. DNA is the chemical in each of our cells that makes up our genes, the instructions for how our cells function. We usually look like our parents because they are the source of our DNA. But DNA can also influence our risk for developing certain diseases, such as some kinds of cancer.

Some genes control when our cells grow, divide into new cells, and die. Genes that help cells grow, divide, or stay alive are called oncogenes. Genes that slow down cell division or cause cells to die at the right time are called tumor suppressor genes. Cancers can be caused by DNA changes that turn on oncogenes or turn off tumor suppressor genes.

Some people with cancer have DNA changes they inherited from a parent that increase their risk for the disease. For example, some people inherit a change (mutation) in the BAP1 tumor suppressor gene, which increases their risk of eye melanoma and some other cancers. When the BAP1 gene is mutated, it doesn’t work normally, which can allow cells with this change to grow out of control.

Most DNA changes linked to cancer are acquired during life rather than inherited before birth. For example, recent research has shown that about 4 out of 5 eye melanomas have changes in either of 2 related genes, GNA11 or GNAQ, which appear to be oncogenes. Other, as of yet unknown, gene changes are probably needed for these cancers to develop as well.

Scientists are studying these and other DNA changes to learn more about them and how they might lead to eye cancer. But it is still not exactly clear what causes these changes to occur in some people and not others.

Signs and symptoms of eye lymphoma


The possible signs and symptoms of eye lymphomas include:

    #Blurred vision or loss of vision
    #Seeing floaters (spots or squiggles drifting in the field of vision)
    #Redness or swelling in the eye
    Sensitivity to light
    #Eye pain (uncommon)

Intraocular lymphoma most often affects both eyes, but it can cause more symptoms in one eye than in the other.

Most of these symptoms are more likely to be caused by other, less serious conditions. For example, floaters can occur as a normal part of the aging process. Still, if you have any of these symptoms, it’s important to see a doctor right away so the cause can be found and treated, if needed.

Many of the exams and tests mentioned below are described in more detail in the section “How is melanoma of the eye diagnosed?”

Eye exam


The doctor will ask about any symptoms you are having and may check your vision and eye movements. During the eye exam, the doctor will use an ophthalmoscope (an instrument with a light and a small magnifying lens) to get a good look inside the eye. If lymphoma is present, the doctor may see that the vitreous (the jelly-like substance that fills most of the inside of the eye) is cloudy.

Imaging tests


Imaging tests use sound waves, x-rays, or magnets to create pictures of the inside of your body.

Ultrasound: Ultrasound is usually done to determine the size, shape, and location of the mass (tumor), especially if the back of the eye can’t be seen during the eye exam.

Magnetic resonance imaging (MRI) scan: An MRI of the head is often done not only to see the eye better, but also to look for lymphoma in the brain or meninges (the thin layers of tissue that cover the brain and spinal cord), which are common sites of spread of this cancer.

Computed tomography (CT) scan: CT scans are used less often than MRI scans for eye lymphoma because they do not provide as much detail.

Positron emission tomography (PET) scan: If a lymphoma has been found, a PET scan can help give the doctor a better idea of whether it has spread to lymph nodes or other parts of the body. A PET scan can also be useful if your doctor thinks the cancer might have spread but doesn’t know where.

For this test, a form of radioactive sugar (known as fluorodeoxyglucose or FDG) is injected into a vein (IV). (The amount of radioactivity is very low and will pass out of the body over the next day or so.) Because cancer cells in the body are growing rapidly, they absorb more of the radioactive sugar. After about an hour, you are moved onto a table in the PET scanner. You lie on the table for about 30 minutes while a special camera creates a picture of areas of radioactivity in the body. The picture is not as detailed as a CT or MRI scan, but it can provide helpful information about whether abnormal areas seen on these tests are likely to be cancer.

Many centers have special machines that can do both a PET and CT scan at the same time (PET/CT scan). This lets the doctor compare areas of higher radioactivity on the PET scan with the more detailed appearance of that area on the CT scan.

For more information on imaging tests, see our document Imaging (Radiology) Tests.

Biopsy


Symptoms and the results of exams and tests might suggest you have intraocular lymphoma, but a biopsy is usually needed to confirm the diagnosis. To biopsy the eye, an ophthalmologist most often does a procedure called a vitrectomy. You may be sedated and get local anesthesia (numbing medicine) or you may get general anesthesia (which puts you in a deep sleep).

The doctor takes a sample of the vitreous gel from inside the eye by inserting very small instruments into the eye, cutting the vitreous, and then sucking some of it out. The cells in the biopsy sample are then sent to a lab to be looked at under a microscope and tested by other special techniques. For more information on the lab tests done on suspected lymphoma specimens, see our document Non-Hodgkin Lymphoma.

Lumbar puncture (spinal tap)


This test is used to look for lymphoma cells in the fluid that surrounds the brain and spinal cord (called cerebrospinal fluid or CSF). It is done in cases of known or suspected eye lymphomas because these cancers often affect the brain or spinal cord.

For this test, you lie on your side with your knees up near your chest. The doctor first numbs an area in the lower part of the back near the spine. A small, hollow needle is then placed between the bones of the spine to withdraw some of the fluid.

The fluid is then examined under a microscope for lymphoma cells. Other tests may be done on the fluid as well.



Source By.........http://www.cancer.org/cancer/eyecancer/detailedguide/eye-cancer-lymphoma-diagnosis

Tuesday, November 10, 2015




Do we know what causes kidney cancer?
Although many risk factors can increase the chance of developing renal cell cancer (RCC), it is not yet clear how some of these risk factors cause kidney cells to become cancerous.

 Changes (mutations) in genes


Researchers are starting to understand how certain changes in the DNA inside normal kidney cells can cause them to become cancerous. DNA is the chemical that makes up our genes − the instructions for how our cells function. We usually look like our parents because they are the source of our DNA. However, DNA affects more than how we look.

Some genes control when our cells grow, divide into new cells, and die. Certain genes that help cells grow, divide, and stay alive are called oncogenes. Others that slow down cell division, or cause cells to die at the right time, are called tumor suppressor genes. Cancers can be caused by DNA changes that turn on oncogenes or turn off tumor suppressor genes.

Inherited gene mutations


Certain inherited DNA changes can lead to conditions running in some families that increase the risk of kidney cancer. These syndromes, which cause a small portion of all kidney cancers, were described in the section “What are the risk factors for kidney cancer?”

For example, VHL, the gene that causes von Hippel-Lindau (VHL) disease, is a tumor suppressor gene. It normally helps keep cells from growing out of control. Mutations (changes) in this gene can be inherited from parents. When the VHL gene is mutated, it is no longer able to suppress abnormal growth, and kidney cancer is more likely to develop. The genes linked to hereditary leiomyoma and renal cell carcinoma (the FH gene), Birt-Hogg-Dube syndrome (the FLCN gene), and familial renal cancer (the SDHB and SDHD genes) are also tumor suppressor genes, and inherited changes in these genes also lead to an increased risk of kidney cancer.

People with hereditary papillary renal cell carcinoma have inherited changes in the MET oncogene that cause it to be turned on all the time. This can lead to uncontrolled cell growth and makes the person more likely to develop papillary RCC.

Acquired gene mutations


Most DNA mutations related to kidney cancer, however, occur during a person’s life rather than having been inherited. These acquired changes in oncogenes and/or tumor suppressor genes may result from factors such as exposure to cancer-causing chemicals (like those found in tobacco smoke), but often what causes these changes is not known. Many gene changes are probably just random events that sometimes happen inside a cell, without having an outside cause.

Most people with sporadic (non-inherited) clear cell RCC have changes in the VHL gene in their tumor cells that have caused it to stop working properly. These changes are acquired during life rather than being inherited.

Other gene changes may also cause renal cell carcinomas. Researchers continue to look for these changes.

Progress has been made in understanding how tobacco increases the risk for developing kidney cancer. Your lungs absorb many of the cancer-causing chemicals in tobacco smoke into the bloodstream. Because your kidneys filter this blood, many of these chemicals become concentrated in the kidneys. Several of these chemicals are known to damage kidney cell DNA in ways that can cause the cells to become cancerous.

Obesity, another risk factor for this cancer, alters the balance of some of the body’s hormones. Researchers are now learning how certain hormones help control the growth (both normal and abnormal) of many different tissues in the body, including the kidneys.

Signs and symptoms of kidney cancer


Early kidney cancers do not usually cause any signs or symptoms, but larger ones might. Some possible signs and symptoms of kidney cancer include:

   # Blood in the urine (hematuria)
   # Low back pain on one side (not caused by injury)
   # A mass (lump) on the side or lower back
   # Fatigue (tiredness)
   # Loss of appetite
   # Weight loss not caused by dieting
   # Fever that is not caused by an infection and that doesn’t go away
   # Anemia (low red blood cell counts)

These signs and symptoms can be caused by kidney cancer (or another type of cancer), but more often they are caused by other, benign, diseases. For example, blood in the urine is most often caused by a bladder or urinary tract infection or a kidney stone. Still, if you have any of these symptoms, see a doctor so that the cause can be found and treated, if needed.


Source By..http://www.cancer.org/cancer/kidneycancer/detailedguide/kidney-cancer-adult-what-causes

Monday, November 9, 2015

What is colorectal cancer?


Colorectal cancer is a term used for cancer that starts in the colon or the rectum. These cancers can also be referred to separately as colon cancer or rectal cancer, depending on where they start. Colon cancer and rectal cancer have many features in common. They are discussed together in this document except for the section about treatment, where they are discussed separately.

The normal digestive system


The colon and rectum are parts of the digestive system, which is also called the gastrointestinal (GI) system (see illustration). The first part of the digestive system (the stomach and small intestine) processes food for energy while the last part (the colon and rectum) absorbs fluid to form solid waste (fecal matter or stool) that then passes from the body. To understand colorectal cancer, it helps to know something about the normal structure of the digestive system and how it works.

After food is chewed and swallowed, it travels through the esophagus to the stomach. There it is partly broken down and then sent to the small intestine, also known as the small bowel. It is called small because it is narrower than the large intestine (colon and rectum), but actually the small intestine is the longest segment of the digestive system ─ about 20 feet. The small intestine continues breaking down the food and absorbs most of the nutrients.

The small intestine joins the large intestine (or large bowel) in the right lower abdomen. Most of the large intestine is made up of the colon, a muscular tube about 5 feet long. The colon absorbs water and salt from the food matter and serves as a storage place for waste matter.

The colon has 4 sections:

    The first section is called the ascending colon. It starts with a small pouch (the cecum) where the small bowel attaches to the colon and extends upward on the right side of the abdomen. The cecum is also where the appendix attaches to the colon.

    The second section is called the transverse colon since it goes across the body from the right to the left side in the upper abdomen.

    The third section, called the descending colon, continues downward on the left side.
    The fourth and last section is known as the sigmoid colon because of its "S" or "sigmoid" shape.

The waste matter that is left after going through the colon is called feces or stool. It goes into the rectum, the final 6 inches of the digestive system, where it is stored until it passes out of the body through the anus.









The wall of the colon and rectum is made up of several layers (see the illustration in the staging section). Colorectal cancer starts in the innermost layer and can grow through some or all of the other layers. Knowing a little about these layers is important, because the stage (extent of spread) of a colorectal cancer depends to a great degree on how deeply it grows into these layers. For more detailed information, please see the section “How is colorectal cancer staged?"

Abnormal growths in the colon or rectum


Most colorectal cancers develop slowly over several years. Before a cancer develops, a growth of tissue or tumor usually begins as a non-cancerous polyp on the inner lining of the colon or rectum. A tumor is abnormal tissue and can be benign (not cancer) or malignant (cancer). A polyp is a benign, non-cancerous tumor. Some polyps can change into cancer but not all do. The chance of changing into a cancer depends on the kind of polyp. The 2 main types of polyps are:

    Adenomatous polyps (adenomas) are polyps that can change into cancer. Because of this, adenomas are called a pre-cancerous condition.
    Hyperplastic polyps and inflammatory polyps, in general, are not pre-cancerous. But some doctors think that some hyperplastic polyps can become pre-cancerous or might be a sign of having a greater risk of developing adenomas and cancer, particularly when these polyps grow in the ascending colon.

Another kind of pre-cancerous condition is called dysplasia. Dysplasia is an area in the lining of the colon or rectum where the cells look abnormal (but not like true cancer cells) when viewed under a microscope. These cells can change into cancer over time. Dysplasia is usually seen in people who have had diseases such as ulcerative colitis or Crohn's disease for many years. Both ulcerative colitis and Crohn's disease cause chronic inflammation of the colon.

Start and spread of colorectal cancer


If cancer forms in a polyp, it can eventually begin to grow into the wall of the colon or rectum. When cancer cells are in the wall, they can then grow into blood vessels or lymph vessels. Lymph vessels are thin, tiny channels that carry away waste and fluid. They first drain into nearby lymph nodes, which are bean-shaped structures containing immune cells that help fight against infections. Once cancer cells spread into blood or lymph vessels, they can travel to nearby lymph nodes or to distant parts of the body, such as the liver. When cancer spreads to distant parts of the body it is called metastasis.

Types of cancer in the colon and rectum


Several types of cancer can start in the colon or rectum.

Adenocarcinomas: More than 95% of colorectal cancers are a type of cancer known as adenocarcinomas. These cancers start in cells that form glands that make mucus to lubricate the inside of the colon and rectum. When doctors talk about colorectal cancer, this is almost always what they are referring to.

Other, less common types of tumors may also start in the colon and rectum. These include:

Carcinoid tumors: These tumors start from specialized hormone-producing cells in the intestine. They are discussed in our document Gastrointestinal Carcinoid Tumors.

Gastrointestinal stromal tumors (GISTs): These tumors start from specialized cells in the wall of the colon called the interstitial cells of Cajal. Some are benign (non-cancerous); others are malignant (cancerous). These tumors can be found anywhere in the digestive tract, but they are unusual in the colon. They are discussed in our document Gastrointestinal Stromal Tumors (GIST).

Lymphomas: These are cancers of immune system cells that typically start in lymph nodes, but they may also start in the colon, rectum, or other organs. Information on lymphomas of the digestive system is included in our document Non-Hodgkin Lymphoma.

Sarcomas: These tumors can start in blood vessels as well as in muscle and connective tissue in the wall of the colon and rectum. Sarcomas of the colon or rectum are rare. They are discussed in our document Sarcoma - Adult Soft Tissue Cancer.

The remainder of this document focuses only on adenocarcinoma of the colon and rectum.

Signs and symptoms of colorectal cancer


Colorectal cancer may cause one or more of the symptoms below. If you have any of the following you should see your doctor:
    #1.A change in bowel habits, such as diarrhea, constipation, or narrowing of the stool, that lasts for more than a few days
    #2.A feeling that you need to have a bowel movement that is not relieved by doing so
    Rectal bleeding
    #3.Blood in the stool which may make it look dark
    #4.Cramping or abdominal (belly) pain
    #5Weakness and fatigue
    #6.Unintended weight loss

Colorectal cancers can bleed. While sometimes the blood can be seen or cause the stool to become darker, often the stool looks normal. The blood loss can build up over time, though, and lead to low red blood cell counts (anemia). Sometimes the first sign of colorectal cancer is a blood test showing a low red blood cell count.

Most of these problems are more often caused by conditions other than colorectal cancer, such as infection, hemorrhoids, irritable bowel syndrome, or inflammatory bowel disease. Still, if you have any of these problems, it's important to see your doctor right away so the cause can be found and treated, if needed.


Source  By....http://www.cancer.org/cancer/colonandrectumcancer/detailedguide/colorectal-cancer-risk-factors

Sunday, November 8, 2015



Signs  and symptoms

 Widespread use of screening mammograms has increased the number of breast cancers found before they cause any symptoms. Still, some breast cancers are not found by mammogram, either because the test was not done or because, even under ideal conditions, mammograms do not find every breast cancer.

The most common symptom of breast cancer is a new lump or mass. A painless, hard mass that has irregular edges is more likely to be cancerous, but breast cancers can be tender, soft, or rounded. They can even be painful. For this reason, it is important to have any new breast mass or lump or breast change checked by a health care professional experienced in diagnosing breast diseases.


 Women who detect any of the following signs or symptoms should tell their doctor (NHS, UK):


    *  A lump in a breast
    * A pain in the armpits or breast that does not seem to be related to the woman's menstrual period
    * Pitting or redness of the skin of the breast; like the skin of an orange
    * A rash around (or on) one of the nipples
    *  A swelling (lump) in one of the armpits
    * An area of thickened tissue in a breast
    * One of the nipples has a discharge; sometimes it may contain blood
    *The nipple changes in appearance; it may become sunken or inverted
    *The size or the shape of the breast changes
    * The nipple-skin or breast-skin may have started to peel, scale or flake.


     
Sometimes a breast cancer can spread to lymph nodes under the arm or around the collar bone and cause a lump or swelling there, even before the original tumor in the breast tissue is large enough to be felt. Swollen lymph nodes should also be reported to your doctor.

Although any of these symptoms can be caused by things other than breast cancer, if you have them, they should be reported to your doctor so that he or she can find the cause.

How is breast cancer treated?

 

This information represents the views of the doctors and nurses serving on the American Cancer Society's Cancer Information Database Editorial Board. These views are based on their interpretation of studies published in medical journals, as well as their own professional experience.
This treatment information is not official policy of the Society and is not intended as medical advice to replace the expertise and judgment of your cancer care team. It is intended to help you and your family make informed decisions, together with your doctor.
Your doctor may have reasons for suggesting a treatment plan different from these general treatment options. Don't hesitate to ask him or her questions about your treatment options.
General types of treatment for breast cancer

The main types of treatment for breast cancer are:

    *Surgery
    *Radiation therapy
    *Chemotherapy
    *Hormone therapy
    *Targeted therapy
    *Bone-directed therapy

Treatments can be classified into broad groups, based on how they work and when they are used.

Local versus systemic therapy


Local therapy is intended to treat a tumor at the site without affecting the rest of the body. Surgery and radiation therapy are examples of local therapies.

Systemic therapy refers to drugs which can be given by mouth or directly into the bloodstream to reach cancer cells anywhere in the body. Chemotherapy, hormone therapy, and targeted therapy are systemic therapies.

Adjuvant and neoadjuvant therapy


Patients who have no detectable cancer after surgery are often given additional treatment to help keep the cancer from coming back. This is known as adjuvant therapy. Doctors believe that even in the early stages of breast cancer, cancer cells may break away from the primary breast tumor and begin to spread. These cells can't be felt on a physical exam or seen on x-rays or other imaging tests, and they cause no symptoms. But they can go on to become new tumors in nearby tissues, other organs, and bones. The goal of adjuvant therapy is to kill these hidden cells. Both systemic therapy (like chemotherapy, hormone therapy, and targeted therapy) and radiation can be used as adjuvant therapy.

Most, but not all, patients benefit from adjuvant therapy. How much you might benefit depends on the stage and characteristics of the cancer and what type of surgery you had. Generally speaking, if the tumor is larger or the cancer has spread to lymph nodes, it is more likely to have spread through the bloodstream, and you are more likely to see a benefit. But there are other features, some of which have been previously discussed, that may determine if a patient should get adjuvant therapy. Recommendations about adjuvant therapy are discussed in the sections on these treatments and in the section on treatment by stage.

Some patients are given treatment, such as chemotherapy or hormone therapy, before surgery. The goal of this treatment is to shrink the tumor in the hope it will allow a less extensive operation to be done. This is called neoadjuvant therapy. Neoadjuvant therapy also lowers the chance of the cancer coming back later. Many patients who get neoadjuvant therapy will not need adjuvant therapy, or will not need as much.

The next few sections offer general information about the types of treatments used for breast cancer. This is followed by a discussion of the typical treatment options based on the stage of the cancer (including non-invasive and invasive breast cancers), plus a small section on breast cancer treatment during pregnancy.


Source By.....http://www.cancer.org/cancer/breastcancer/detailedguide/breast-cancer-treating-general-info
http://www.medicalnewstoday.com/articles/37136.php

Saturday, November 7, 2015

What is pancreatic cancer?

 To understand pancreatic cancer, it helps to know about the pancreas and what it does.

The normal pancreas

The pancreas is an organ located behind the stomach. It is shaped a little bit like a fish with a wide head, a tapering body, and a narrow, pointed tail. In adults it is about 6 inches long but less than 2 inches wide. The head of the pancreas is on the right side of the abdomen (belly), behind where the stomach meets the duodenum (the first part of the small intestine). The body of the pancreas is behind the stomach, and the tail of the pancreas is on the left side of the abdomen next to the spleen.

The pancreas contains 2 different types of glands: exocrine and endocrine.

The exocrine glands make pancreatic “juice,” which is released into the intestines. This juice contains enzymes that help you digest the food you eat. Without these, some of the food would just pass through your intestines without being absorbed. The enzymes are released into tiny tubes called ducts. These tiny ducts merge to form larger ducts, which empty into the pancreatic duct. The pancreatic duct merges with the common bile duct (the duct that carries bile from the liver), and empties the pancreatic juice into the duodenum (the first part of the small intestine) at the ampulla of Vater. More than 95% of the cells in the pancreas are in the exocrine glands and ducts.

A small percentage of the cells in the pancreas are endocrine cells. These cells are in small clusters called islets (or islets of Langerhans). The islets make important hormones, such as insulin and glucagon, and release them directly into the blood. Insulin reduces the amount of sugar in the blood, while glucagon increases it.

Benign and precancerous growths in the pancreas


Not all growths in the pancreas are cancer. Some growths are simply benign (not cancer), while others might become cancer over time if left untreated (known as precancers). Because people are getting imaging tests such as CT scans more often than in the past (for a number of reasons), these types of pancreatic growths are now being found more often.

Serous cystic neoplasms (SCNs) (also known as serous cystadenomas) are tumors that have sacs (cysts) filled with watery fluid. SCNs are almost always benign, and most don’t need to be treated unless they grow large or cause symptoms.

Mucinous cystic neoplasms (MCNs) (also known as mucinous cystadenomas) are slow-growing tumors that have cysts filled with a jelly-like substance called mucin. These tumors usually start in the body or tail of the pancreas. While they are not cancer, some of them can progress to cancer over time if not treated. Whether these tumors need to be removed or can just be followed closely over time depends on several factors, such as their size, rate of growth, how they look on imaging tests, and if they are causing symptoms.

Intraductal papillary mucinous neoplasms (IPMNs) are benign tumors that grow in the pancreatic ducts. Like MCNs, these tumors make mucin, and they can sometimes become cancer over time if not treated. Some IPMNs can just be followed closely over time, but as with MCNs, some might need to be removed with surgery if they have concerning features.

Pancreatic cancers


The exocrine cells and endocrine cells of the pancreas form different types of tumors. It’s very important to distinguish between exocrine and endocrine cancers of the pancreas. They have distinct risk factors and causes, have different signs and symptoms, are diagnosed using different tests, are treated in different ways, and have different outlooks.

Exocrine tumors


Exocrine tumors are by far the most common type of pancreas cancer. When someone says that they have pancreatic cancer, they usually mean an exocrine pancreatic cancer.

Pancreatic adenocarcinoma: An adenocarcinoma is a cancer that starts in gland cells. About 95% of cancers of the exocrine pancreas are adenocarcinomas. These cancers usually begin in the ducts of the pancreas. But sometimes they develop from the cells that make the pancreatic enzymes, in which case they are called acinar cell carcinomas.

Less common types of cancers: Other cancers of the exocrine pancreas include adenosquamous carcinomas, squamous cell carcinomas, signet ring cell carcinomas, undifferentiated carcinomas, and undifferentiated carcinomas with giant cells. These types are distinguished from one another based on how they look under the microscope.

Solid pseudopapillary neoplasms (SPNs): These are rare, slow-growing tumors that almost always occur in young women. Even though these tumors tend to grow slowly, they can sometimes spread to other parts of the body, so they are best treated with surgery. The outlook for people with these tumors is usually very good.

Ampullary cancer (carcinoma of the ampulla of Vater): This cancer starts in the ampulla of Vater, which is where the bile duct and pancreatic duct come together and empty into the small intestine. Ampullary cancers aren’t technically pancreatic cancers, but they are included in this document because their treatments are very similar.

Ampullary cancers often block the bile duct while they are still small and have not spread far. This blockage causes bile to build up in the body, which leads to yellowing of the skin and eyes (jaundice) and can turn urine dark. Because of this, these cancers are usually found at an earlier stage than most pancreatic cancers, and they usually have a better prognosis (outlook) than typical pancreatic cancers.
Endocrine tumors

Tumors of the endocrine pancreas are uncommon, making up less than 4% of all pancreatic cancers. As a group, they are sometimes known as pancreatic neuroendocrine tumors (NETs) or islet cell tumors.

Pancreatic NETs can be benign or malignant (cancer). Benign and malignant tumors can look alike under a microscope, so it isn’t always clear whether or not a pancreatic NET is cancer. Sometimes the diagnosis only becomes clear when the tumor spreads outside of the pancreas.

There are many types of pancreatic NETs.

Functioning tumors: About half of pancreatic NETs make hormones that are released into the blood and cause symptoms. These are called functioning tumors. Each one is named for the type of hormone-making cell it starts in.

    Gastrinomas come from cells that make gastrin. About half of gastrinomas are cancers.
    Insulinomas come from cells that make insulin. Most insulinomas are benign (not cancers).
    Glucagonomas come from cells that make glucagon. Most glucagonomas are cancers.
    Somatostatinomas come from cells that make somatostatin. Most somatostatinomas are cancers.
    VIPomas come from cells that make vasoactive intestinal peptide (VIP). Most VIPomas are cancers.
    PPomas come from cells that make pancreatic polypeptide. Most PPomas are cancers.

The most common types of functioning NETs are gastrinomas and insulinomas. The other types occur very rarely.

Non-functioning tumors: These tumors don’t make enough excess hormones to cause symptoms. They are more likely to be cancer than functioning tumors. Because they don’t make excess hormones that cause symptoms, they can often grow quite large before they are found.

Carcinoid tumors: These are another type of NET that rarely can start in the pancreas, although they are much more common in other parts of the digestive system. These tumors often make serotonin (also called 5-HT) or its precursor, 5-HTP.

The treatment and outlook for pancreatic NETs depend on the specific tumor type and the stage (extent) of the tumor, but the outlook is generally better than that of pancreatic exocrine cancers.

Signs and symptoms of pancreatic cancer


The symptoms of exocrine and endocrine pancreatic cancers are often different, so they are described separately.

Having one or more of the symptoms below does not mean you have pancreatic cancer. In fact, many of these symptoms are more likely to be caused by other conditions. Still, if you have any of these symptoms, it’s important to have them checked by a doctor so that the cause can be found and treated, if needed.

Signs and symptoms of exocrine pancreatic cancer


Early pancreatic cancers often do not cause any signs or symptoms. By the time they do cause symptoms, they have often already grown through the pancreas or spread beyond it.

Jaundice and related symptoms


Jaundice is yellowing of the eyes and skin. Most people with pancreatic cancer (and virtually all people with ampullary cancer) will have jaundice as one of their first symptoms.

Jaundice is caused by the buildup of bilirubin, a dark yellow-brown substance made in the liver. Normally, the liver excretes bilirubin as part of a liquid called bile. Bile goes through the common bile duct into the intestines, eventually leaving the body in the stool. When the common bile duct becomes blocked, bile can’t reach the intestines, and the level of bilirubin in the body builds up.

Cancers that start in the head of the pancreas are near the common bile duct. These cancers can press on the duct and cause jaundice while they are still fairly small, which may allow these tumors to be found at an early stage. But cancers that start in the body or tail of the pancreas don’t press on the duct until they have spread through the pancreas. By this time, the cancer has often spread beyond the pancreas as well.

When pancreatic cancer spreads, it often goes to the liver. This can also lead to jaundice.

Dark urine: Sometimes, the first sign of jaundice is darkening of the urine from bilirubin. As bilirubin levels in the blood increase, the urine becomes brown in color.

Light-colored stools: If the bile duct is blocked, bile (and bilirubin) can’t get through to the bowel. When this happens, a person might notice their stools becoming lighter in color.

Itchy skin: When bilirubin builds up in the skin, it can start to itch as well as turning yellow.

Pancreatic cancer is not the most common cause of jaundice. Other causes, such as gallstones, hepatitis, and other liver diseases, are much more common.

Abdominal or back pain


Pain in the abdomen (belly) or back is common in pancreatic cancer. Cancers that start in the body or tail of the pancreas can grow fairly large and start to press on other nearby organs, causing pain. The cancer may also spread to the nerves surrounding the pancreas, which often causes back pain. Of course, pain in the abdomen or back is fairly common and is most often caused by something other than pancreatic cancer.

Weight loss and poor appetite


Unintended weight loss is very common in people with pancreatic cancer. These people often have little or no appetite.

Digestive problems


Pale, greasy stools: If cancer blocks the release of the pancreatic juice into the intestine, a person might not be able to digest fatty foods. The undigested fat can cause stools to be unusually pale, bulky, greasy, and to float in the toilet.

Nausea and vomiting: If the cancer presses on the far end of the stomach it can partly block it, making it hard for food to get through. This can cause nausea, vomiting, and pain that tend to be worse after eating.

Gallbladder enlargement

If the cancer blocks the bile duct, bile can build up in the gallbladder, which then becomes enlarged. This can sometimes be felt by a doctor (as a large lump under the right ribcage) during a physical exam. It can also be detected by imaging tests.

Blood clots

Sometimes, the first clue that someone has pancreatic cancer is the development of a blood clot in a large vein, often in the leg. This is called a deep venous thrombosis or DVT. Symptoms can include pain, swelling, redness, and warmth in the affected leg. Sometimes a piece of the clot can break off and travel to the lungs, which might make it hard to breathe or cause chest pain. A blood clot in the lungs is called a pulmonary embolism or PE.

Still, having a blood clot does not usually mean that you have cancer. Most blood clots are caused by other things.

Fatty tissue abnormalities

Some people with pancreatic cancer develop an uneven texture of the fatty tissue underneath the skin. This is caused by the release of the pancreatic enzymes that digest fat.
Diabetes

Rarely, pancreatic cancers cause diabetes (high blood sugar) because they destroy the insulin-making cells. Symptoms can include feeling thirsty and hungry, and having to urinate often. More often, there are small changes in blood sugar levels that don’t cause symptoms of diabetes but can still be detected with blood tests.



Source By....http://www.cancer.org/cancer/pancreaticcancer/detailedguide/pancreatic-cancer-what-is-pancreatic-cancer

Friday, November 6, 2015

What is bone cancer?

Normal bone tissue

Bone is the supporting framework of your body. Most bones are hollow. The outer part of bones is a network of fibrous tissue called matrix onto which calcium salts are laid down.


The hard outer layer of bones is made of compact (cortical) bone, which covers the lighter spongy (trabecular) bone inside. The outside of the bone is covered with a layer of fibrous tissue called periosteum. Some bones are hollow and have a space called the medullary cavity which contains the soft tissue called bone marrow (discussed below). The tissue lining the medullary cavity is called endosteum. At each end of the bone is a zone of a softer form of bone-like tissue called cartilage.

Cartilage is softer than bone but more firm than most tissues. It is made of a fibrous tissue matrix mixed with a gel-like substance that does not contain much calcium.

Most bones start out as cartilage. The body then lays calcium down onto the cartilage to form bone. After the bone is formed, some cartilage may remain at the ends to act as a cushion between bones. This cartilage, along with ligaments and some other tissues connect bones to form a joint. In adults, cartilage is mainly found at the end of some bones as part of a joint. It is also seen at the place in the chest where the ribs meet the sternum (breastbone) and in parts of the face. The trachea (windpipe), larynx (voice box), and the outer part of the ear are other structures that contain cartilage.

Bone itself is very hard and strong. Some bone is able to support as much as 12,000 pounds per square inch. It takes as much as 1,200 to 1,800 pounds of pressure to break the femur (thigh bone). The bone itself contains 2 kinds of cells. The osteoblast is the cell that lays down new bone, and the osteoclast is the cell that dissolves old bone. Bone often looks as if it doesn’t change much, but the truth is that it is very active. Throughout our bodies, new bone is always forming while old bone is dissolving.

In some bones the marrow is only fatty tissue. The marrow in other bones is a mixture of fat cells and blood-forming cells. The blood-forming cells produce red blood cells, white blood cells, and blood platelets. Other cells in the marrow include plasma cells, fibroblasts, and reticuloendothelial cells.

Cells from any of these tissues can develop into a cancer.

Signs and symptoms of bone cancer

Pain

Pain in the affected bone is the most common complaint of patients with bone cancer. At first, the pain is not constant. It may be worse at night or when the bone is used (for example, leg pain when walking). As the cancer grows, the pain will be there all the time. The pain increases with activity and the person might limp if a leg is involved.

Swelling


Swelling in the area of the pain may not occur until weeks later. It might be possible to feel a lump or mass depending on the location of the tumor.

Cancers in the bones of the neck can cause a lump in the back of the throat that can lead to trouble swallowing or make it hard to breathe.

Fractures


Bone cancer can weaken the bone it develops in, but most of the time the bones do not fracture (break). People with a fracture next to or through a bone cancer usually describe sudden severe pain in a limb that had been sore for a few months.

Other symptoms


Cancer in the bones of the spine can press on nerves, leading to numbness and tingling or even weakness.

Cancer can cause weight loss and fatigue. If the cancer spreads to internal organs it may cause other symptoms, too. For example, if the cancer spreads to the lung, you may have trouble breathing.

Any of these symptoms are more often due to conditions other than cancer, such as injuries or arthritis. Still, if these problems go on for a long time without a known reason, you should see your doctor.

How is bone cancer treated?

This information represents the views of the doctors and nurses serving on the American Cancer Society’s Cancer Information Database Editorial Board. These views are based on their interpretation of studies published in medical journals, as well as their own professional experience.
The treatment information in this document is not official policy of the Society and is not intended as medical advice to replace the expertise and judgment of your cancer care team. It is intended to help you and your family make informed decisions, together with your doctor.
Your doctor may have reasons for suggesting a treatment plan different from these general treatment options. Don’t hesitate to ask him or her questions about your treatment options.


Depending on the type and stage of your cancer, you may need more than one type of treatment. Doctors on your cancer treatment team may include:
    An orthopedic surgeon: a doctor who uses surgery to treat bone and joint problems
    An orthopedic oncologist: an orthopedic surgeon that specializes in treating cancer of the bones and joints.
    A radiation oncologist: a doctor who uses radiation to treat cancer
    A medical oncologist: a doctor who uses chemotherapy and other medicines to treat cancer.

Many other specialists may be involved in your care as well, including nurse practitioners, nurses, psychologists, social workers, rehabilitation specialists, and other health professionals.

The main types of treatment for bone cancer are:
    *Surgery
    *Radiation
    *Chemotherapy
    *Targeted therapy

Often, more than one type of treatment is used. For information about some of the most common approaches used based on the extent of the disease, see the section “Treating specific bone cancers.”

It is important to discuss all of your treatment options, including their goals and possible side effects, with your doctors to help make the decision that best fits your needs. It’s also very important to ask questions if there is anything you’re not sure about. You can find some good questions to ask in the section.

             
Source By...   http://www.cancer.org/cancer/bonecancer/detailedguide/bone-cancer-what-is-bone-cancer