Showing posts with label Diagnosis. Show all posts
Showing posts with label Diagnosis. Show all posts

Brain Cancer: Diagnosis and Prevention

The very first diagnostic step is a neurological examination to check eye movement and vision, hearing, sensation, reflexes, balance and coordination, thinking and memory. After neurological examination is over expert may suggest imaging studies and laboratory test for further information about the tumor and its location. Diagnostic tests are often used after treatment to monitor the outcome and recurrence of tumors. Diagnosis for brain cancer may include computerized tomography scan known as CT or CT scan, magnetic resonance imaging or MRI, bone scan and lumbar puncture.
CT scan stands for Computerized Tomography: A CT scan directs x-rays from multiple angles to a specific body part like various cross sections of tissues and bony structures. This can help identify the tumor's location and can sometimes help to determine the tumor type. Additionally it can also detect swelling, bleeding or other conditions associated with the tumor. Magnetic resonance imaging combines computer technology, a magnetic field and radio waves to produce a two dimensional image of the patients anatomy. This process is radiation free and the radio waves are harmless. Positron emission tomography scans create color coded pictures of brain activity by measuring low dose radioactive levels. The PET scan measures the consumption rate of sugar substance in different parts of brain. This can be helpful in detecting recurrent tumor growth. Plain x-ray films of the head may be used to determine the condition of the head and the effect of the tumor on bony structures.
Brain cancer prevention can help person to prevent or reduce the seriousness of the disease they are affected with. There are certain steps that help to prevent the disease like exploring his or her family history and find out what diseases run in the family. If one finds any signs of the disease an immediate visit to the doctor is warranted. Avoiding things causing this serious disease like smoking, drinking alcohol and cell phones as cell phones give off radioactive waves which attack brain cells. Get a regularly health diet because healthier living promotes longer happier lives, read those books that guide you about how this serious disease is caused and what kind of symptoms they have in common. Make sure that our environment is clean as it is very beneficial to our overall health.
Brain cancer originates in the brain is called primary brain tumor. It occurs at any age. But most probably it happens in childhood and can lead to adult. It can spread and destroy nearby parts of brain. There are many instances where effects of brain cancer have spread to the brain from others parts of the body like breast cancer, liver cancer, lung cancer and so on. Brain cancer often occurs within the same family members, inheritance is also a responsible cause of brain cancer.
Treatment of brain cancer depends on the diagnosis. Brain cancer treatments involve combination of surgery, radiation and chemotherapy. Some tumors require several different surgical procedures, and some can be treated with radiation therapy. But the initial treatment of a brain tumor may include steroid medications to reduce growth and inflammation of brain tissue. Anticonvulsant medications may help to prevent or control illness. Drugs used in cancer chemotherapy specifically attack cells that promote division. These drugs are useful because cancer cells spend more of their time dividing and reproducing than normal cells do.-By: Mark Lee

Pleural Mesothelioma - Symptoms, Diagnosis and Treatment

Pleural Mesothelioma is the most common type of mesothelioma which is characterized by the formation of cancerous tumors in pleura which is the protective lining of lung surrounding the chest cavity and diaphragm.
Pleural Mesothelioma Causes
Like other types of mesothelioma, pleural mesothelioma is also connected to asbestos exposure. Once asbestos fibers enter the body through inhalation they lodged on pleura and start changing its nature after passing one or two decades. These changes occur in the form of irritation and inflammation which results in the formation and proliferation of cancerous cells. Such developments lead to pleural thickening which further aggravates the condition by building fluid in chest cavity. Fluid building in pleural cavity put pressure on lungs and makes it difficult to breathe easily. At this stage patient feels that something is going wrong in its chest region which is creating problem in normal breathing and causing persistent pain and cough for him.
Pleural Mesothelioma Symptoms
Various symptoms of pleural mesothelioma include:
* Persistent Cough
* Persistent Pain in Chest
* Lump Formation in Chest Area
* Hemoptysis (coughing up blood)
* Dyspnea (Shortness of breath)
* Dysphagia (Difficulty in swallowing)
* Weight Loss
* Fatigue and Fever
Pleural Mesothelioma Diagnosis
In order to diagnose pleural mesothelioma imaging techniques including X-rays, MRI and CT scan are applied along with taking patients' medical history and current health state into account. All these measures helps in diagnosing the presence of cancerous cells inside the body and level of damage already occurred to pleural lining. If necessary then biopsy can also be recommended to take out the sample of fluid building around pleura through minor surgical process. This sample is then tested into laboratory in order to trace the presence of cancerous cells inside pleural cavity.
Pleural Mesothelioma Treatment
Like other types of mesothelioma it is also treated by applying one or combination of given treatment methods:
1- Radiotherapy (using radiations to destroy cancer cells)
2- Chemotherapy (injecting chemicals directly to affected part of pleura)
3- Surgery (cutting out the damaged portion completely)
The selection of treatment method depends upon the health condition of the patient and level of damage occurred to his body. Early diagnosis makes it easier to treat mesothelioma. So if anyone is feeling above mentioned symptoms then don't take it easy and take an appointment with your physician to find out the actual cause of this internal body disturbance.
Pleural Mesothelioma

Bone Cancer - Causes, Symptoms, Diagnosis, Treatment and Prognosis

Bone cancer is rare and accounts for less than 1% of all new tumors. Not all bone tumors are fatal in fact benign (non cancerous) abnormalities are more common than malignant ones. Most are secondary and have been spread from another site. Primary bone cancer which starts in the bone is quite rare constituting less than one per cent of all malignant tumors. They are more common in males, especially in children and adolescents. The most common type of primary cancer is osteosarcoma. This type of carcinoma usually affects young adults. It can affect any bone, but the arms, legs and pelvis are more commonly affected. Other less common forms of primary bone cancer include Ewing sarcoma, malignant fibrous histiocytoma and chondrosarcoma.
Primary Bone Cancer
The causes of primary bone tumours are not known; however, adults who have Pagets disease (a bone disease) may have an increased risk.
Secondary bone cancer
Secondary bone cancer is the most common bone cancer. It is a carcinoma that starts somewhere else in the body and spreads (metastasises) to the bone. The most common cancers that spread to the bone originate in the breast, prostate, lung, kidney and thyroid.
Reticulum cell sarcoma of the bone
A cancerous tumor of the bone marrow presenting in more males than females.
Leukaemia
Cancer of the blood, which starts in the bone marrow
Symptoms of bore cancer
Symptoms tend to develop slowly and depend on the type, location, and size of the tumor. The signs and symptoms of bone carcinoma include: painful bones and joints, swelling of bones and joints, problems with movement, susceptibility to fractures. Less common symptoms include: unexplained weight loss, tiredness, fever and sweating.
Remember this conditionr is very rare so if you have any of these symptoms it is likely to be caused by another condition. Always see your doctor if you have for a diagnosis.
Causes
Although bone cancer does not have a clearly defined cause, researchers have identified several factors that increase the likelihood of developing these tumors. A small number of bone cancers are due to heredity.
Diagnosis
Bone cancer can present itself in any of the bones of the body, but it is diagnosed most often in the long bones of the arms and legs.
Diagnosing bone cancer involves a number of tests, including: X-rays and bone scans to show the exact location and size of the cancer (these are always done prior to biopsy), bone biopsy where a small sample of the cancer is removed from the bone and examined in the laboratory for the presence of malignant cells, Magnetic Resonance Imaging (MRI) scan similar to a CT scan but uses magnetism instead of x-rays to build three-dimensional pictures of your body.
Treatment
The treatment and prognosis depends upon multiple factors including the type and extent of the cancer, the patient's age and overall health status. Tumors may be treated with surgery, radiation therapy, chemotherapy, or a combination of these.
Primary bone cancers:
The tumor, surrounding bone tissue and nearby lymph nodes are surgically removed. In severe cases, the affected limb may need to be amputated, but this is rare. Treatment may also include radiotherapy (x-rays to target and kill the cancer cells) and chemotherapy (anti-cancer drugs). These may be given before surgery, to shrink the cancer and/or afterward to destroy any remaining cancer cells.
Secondary bone cancer:
Treatment depends on the treatment for the original tumor, but usually includes chemotherapy, radiotherapy or hormone therapy. Surgery may be needed to strengthen the affected bone.
Prognosis
Overall, the chance of recovery (prognosis) for bone cancers has improved significantly since the development of modern chemotherapy. The chance of recovery will depend on a variety of influences; if the cancer has spread, the type of cancer, the size of the tumour, location, the person's general health and other individual factors.
If the tumor is very small and localized, the five-year survival rate is close to 90 percent. If the cancer has begun to spread, however, survival becomes more difficult. The five-year survival rate is only about 60 percent, and the prognosis is poor once the cancer spreads.
Bone cancer in cats and dogs
Bone carcinoma in dogs and cats can be a challenging disorder. Osteosarcoma is by far the most common bone tumour if dogs, usually striking the leg bones of larger breeds. Chemotherapy significantly prolongs the survival of animals with osteosarcoma when used in conjunction with surgery. For dogs Cisplatin alone or in combination with doxorubicin markedly improves survival time to a median of 8-10 months with the percentage of dogs alive after11 months at 50%.
Feline Osteosarcoma unlike its canine counterpart it has a much lower rate of metastasis and longer term survival can be expected with complete excision. Median survival for cats with osteosarcoma is approximately 2 years with many cats outreaching that.

Diagnosing Celiac Disease and Gluten Sensitivity

Celiac disease, also known as gluten sensitive enteropathy is very common but frequently missed. It is an autoimmune disease of intestinal damage due to gluten in people who are genetically predisposed. Classic Celiac disease is diagnosed by abnormal blood tests and an abnormal
appearing intestine on biopsy and symptoms that resolve with a gluten free diet.
Several blood tests exist for Celiac disease. They have varying degrees of accuracy. Some are more sensitive, meaning they will be positive in milder forms of the disease but are not specific, meaning a positive test may not indicate Celiac disease. Others are felt to be very specific, meaning that when they are positive, it is almost certain you have the disease.
The most specific tests are tests for Celiac disease endomysial antibodies (EMA) and
tissue transglutaminase antibody (tTG) tests. These two tests are IgA based tests and can be negative if you are deficient in the immunoglobin IgA, which occurs in 10-20% of people with Celiac. When either EMA or tTG are positive Celiac disease is very likely and usually the intestine biopsy is positive. Recent studies indicate that the tTG may only be positive in 40% of true Celiacs when mild degrees of intestine damage are present on biopsy. Seronegative Celiac, meaning the blood tests are negative but the biopsy is positive, may occur in up to 20% of Celiacs.
Antibodies for gliadin (AGA), the toxic fraction of gluten are considered very sensitive but not specific for Celiac disease. Newer assays for AGA antibodies for gluten that has undergone a chemical change
called deamidation appear to be more specific for Celiac disease (Gliadin II,
Inova) than the older gliadin tests. They also may be as or more accurate than EMA and tTG
antibody tests but are not yet widely available.
The most distressing problem for people with lesser forms of gluten intolerance who have blood tests and/or biopsies that are normal or borderline yet respond to a gluten free diet is either not being taken seriously or knowing for sure if they are sensitive to gluten. For these individuals stool
antibody testing for antigliadin and tTG have been helpful. Such stool testing has been performed in research labs and published in a few studies but are only recently available through the commercial lab, Enterolab. Founded by a former Baylor research gastroenterologist, Dr Ken Fine, the tests are available to people online without a doctors order but are not generally covered by insurance. Dr. Fine, who patented the test, has yet to publish the results of his findings in a peer reviewed journal so his tests are not widely accepted. However, his unpublished data and the clinical experience of some of us who have used his test have
indicated the tests are very sensitive for signs of gluten sensitivity. He reports that they are 100% sensitive for Celiac disease and highly sensitive
for gluten sensitivity of lesser degrees. In the presence of symptoms, that reverse on a gluten-free diet,
abnormal stool antibody levels can be found in most people before blood tests or biopsies become
abnormal.
Small intestine biopsies during upper gastrointestinal endoscopy
are considered the "gold standard" for the diagnosis of Celiac disease.
However, recent studies have demonstrated that some people with gluten sensitivity, especially relatives of Celiacs
with little or no symptoms, have changes from gluten injury to the intestine that can not be seen with normal microscope examination. They can only be seen with special stains not routinely done or with a research electron microscope. The special stains are known as immunohistochemistry stains. They stain specialized white
blood cells called lymphocytes in the intestinal lining tips or villi. When these lymphocytes are increased it is known as intraepithelial lymphocytosis or increased IELs and it is the earliest sign
of gluten induced injury or irritation. Electron microscopy also reveals very early ultrastructural changes in some individuals when blood tests and standard biopsy examination are normal. When people who have these changes are
offered the option of a gluten-free diet they usually responded favorably. In contrast, those who continue to eat gluten often later developed classic Celiac disease.
What these studies suggest is that a "normal small intestine biopsy" may exclude
Celiac disease as defined by strict criteria but it is not a gold standard for detecting gluten sensitivity. This fact is appreciated by many individuals who have respond to a gluten-free diet they start
based on their symptoms, family history, suggestive blood test or stool antibody
test(s).
Another source of confusion is in the genetics of Celiac and gluten sensitivity.
Testing for specific blood type patterns on white blood cells known as HLA
DQ2 and DQ8 is increasingly being employed to determine if a person carries either of the two gene
pattern present in 95-98% of Celiacs and predisposing them to the development of Celiac disease. Some use the absence of these two patterns
as a way of excluding the possibility of Celiac disease and the need for testing or
gluten-free diet. However, there are rare reports of documented Celiac disease in people who are DQ2 and
DQ8 negative. Moreover, recent studies indicate other DQ
patterns may be associated with gluten sensitivity though unlikely to
predispose to classic Celiac disease.
Testing for all the DQ patterns is advocated by Dr. Fine, based on his
experience with stool antibody test results. He reports that other DQ types are
associated with elevated levels of gliadin and tTG in the stool and symptoms that respond to a gluten-free diet.
According to his unpublished data, all the DQ types except DQ4 are associated with
a risk of intolerance to gluten. Therefore, testing for all the DQ types allows a person to
determine if they carry one of the two high risk gene types for Celiac disease or
any of the other "minor DQ" genes Fine has found associated with gluten sensitivity.
Enterolab's stool testing for gliadin antibodies and tissue
transglutaminase antibodies, though not widely accepted, have gained favor in the lay
public's opinion as an option for determining sensitivity to gluten either despite negative blood tests and/or biopsies or in place of the more invasive tests. Most doctors still recommend the accepted blood tests and small
bowel biopsy for confirmation of Celiac. Though the reports in the lay community
are overwhelmingly positive they have not been subjected to peer review in
the medical community pending Dr. Fine publishing his data or other researchers reproducing his results.
However, doctors open to
the broader problem of gluten
sensitivity are reporting these tests helpful in many patients suspected of gluten
intolerance. Especially when someone has symptoms consistent with gluten sensitivity but has negative or inconclusive blood tests and/or biopsies these tests may be very helpful though some are not certain
how to interpret the tests. The national Celiac organizations are uncertain about how to
comment on their application without published research though a recent article
in the British Medical Journal did show stool tests highly specific for Celiac. Dr.
Fine has publicly commented that his unpublished data demonstrates those with
abnormal stool tests indicating gluten sensitivity
overwhelmingly respond favorably to a gluten free diet with improvement of
symptoms and general quality of life.
Another problem is that there are not universally agreed upon definitions for gluten sensitivity or intolerance. This becomes especially difficult for those who do not meet strict criteria for Celiac disease yet may have abnormal tests and/or symptoms that respond to a gluten-free diet. Those individuals become confused when they try to find information but do not have a formal diagnosis of Celiac disease. Consensus in the medical community on definitions and more research in this area is greatly needed.
The few doctors who appreciate the spectrum of gluten
intolerance or sensitivity are outnumbered by the medical majority that continue to
insist on strict criteria for diagnosis for Celiac disease before recommending a
gluten-free diet. Doctors either unfamiliar with the limitations of the tests as documented by Celiac research or who insist on the
strict criteria for Celiac being the only indication for recommending a gluten free
diet unfortunately may confuse or frustrate gluten sensitive individuals. Some of these people then seek answers on the internet or from alternative practitioners. Many have their diagnosis missed, challenged, dismissed, or are misinformed. As a result they fail to benefit from the health