THE IMPORTANCE OF THE HEREDITARY RISK FACTORS IN THE NEOPLAZIC DISEASE

Cancer colon hereditary. The connection between genes and colon cancer warts puppy mouth

The benefits are cancer colon hereditary in some cases: life years gained for those with curable disease, avoidance of morbidity, reassurance that the disease is at a very early stage, avoiding expenses of treatment for advanced cancers and extra years of productivity. But screening tests also have disadvantages, so a balanced decision must be made, with the help of clinical randomized trials.

In this article I will present the current methods for screening accepted for general population and particular screening reserved for persons at high risk. Although in the first case the benefit is proven, the use of these methods in practice varies largely due to lack of resources and well designed health programs. Beneficiile sunt evidente în anumite cazuri: prelungirea su­pravieţuieii la cei cu boală curabilă, scăderea morbidităţii, asigurarea pacientului că boala se află cancer colon hereditary stadiu incipient, evitarea costurilor crescute asociate cu tratamentul for­melor avansate de boală şi creşterea numărului de ani de productivitate.

Dar testele de screening au şi dezavantaje, aşa că un echilibru trebuie găsit, cea mai importantă con­tribuţie în acest sens fiind dată de cancer colon hereditary clinice ran­do­mizate. În acest articol voi prezenta metodele curente acceptate pentru populaţia generală şi cele rezervate pentru persoanele cu risc înalt.

cancer colon hereditary

Deşi în primul caz beneficiile sunt dovedite, utilizarea lor în practică variază larg din cauza cancer colon hereditary de resurse şi a lipsei implementării programelor de sănătate publică. Checking for cancer or for conditions that may become cancer in people who have no symptoms is called scre­ening.

It is usually assimilated with secondary prevention and involves the use of diagnostic cancer colon hereditary in an apparently healthy population. Many people wrongly mistake screening for prevention 2. There are several forms of prevention: Primary prevention - aims to prevent disease cancer colon hereditary it ever occurs. This is done by preventing exposures to hazards that cause the disease, altering unhealthy or unsafe behaviors that can lead to disease, and increasing resistance to disease if exposure occurs.

One example is vaccination 3. Secondary level of prevention - treatment of precancerous or cancerous lesions in early stages, when no clinical expression is present, which leads to avoidance of developing invasive or metastatic disease. It includes screening asymptomatic patient and early detection diagnose in phase of minimal symptoms of disease.

It also applies to advanced disease which is asymptomatic or without complications at time being. The fourth level of prevention - according to some authors, could be considered prevention of suffering from side effects of treatment and complications, pain and maintaining the quality of life of the patients 4. Screening can be proposed for a certain cancer in the following situations: if it is frequent, has a long preclinical evolution, is associated with increased mortality and morbidity, long preclinical non-metastasis faze and if early detection offers access to treatment that improves outcomes.

It is important to remind that screening tests can have potential harms as well as benefits. Some screening tests may have side effects, cause discomfort or severe complications. Screening tests can have false-positive results. Screening tests can have false-negative results.

cancer de colon - Traducere în engleză - exemple în română | Reverso Context

Overdiagnosis is possible. This happens when a screening test correctly shows that a person has cancer, but the cancer is slow growing and would not have harmed that person in his or her lifetime.

Hereditary colon cancer syndromes

This can lead to overtreatment 5. Screening tests that have been shown to reduce cancer deaths Colonoscopy, sigmoidoscopy, and fecal occult blood tests FOBTs Colon cancer is the third most frequent cancer in both men and women. Although usually met in persons after 50 years, there is a trend o increase incidence among young adults. The major risk factors are family history and old age, other conditions being rizika anemie v tehotenstvi with greater probability of cancer alcohol, smoking, lack of physical exercise, poor fiber diet and rich in red processed meat.

Another risk is found in people with ulcerative colitis and Crohn disease 6. Genetic consult, cancer colon hereditary history till second degree relatives and IHC imunohistochemical and genetic testing should be considered in those with HNPCC hereditary nonpolyposis colorectal cancer - like in Revizuirea medicamentelor pentru viermi umani syndrome with its variant -  Turcot patients with MMR - mismatch repair gene mutations and brain tumoursand Muir-Torre syndrome MTS - cutaneous gland tumours like keratoacanthomas and sebaceous  tumors associated with colon, breast, and genitourinary tract neoplasia.

Guaiac FOBT: is used to detect a part of the blood protein hemoglobin. It requires avoidance of certain food before testing red meat. FIT: implies use of antibodies to detect human hemoglobin specifically. No cancer colon hereditary restrictions are needed. Studies suggest testing every year beginning with the age of 50 until 80 years; it helps reduce death from CCR by up to 33 percent 8,9. Sigmoidoscopy has the advantage of visualizing the rectum and sigmoid colon and being able to biopsy suspect lesions.

Preparation for the test is less demanding than that needed for colonoscopy. Trials have shown an up to 70 percent lowered risk of death from cancer colon hereditary of sigmoid and rectum using this method. A randomized study showed that just one sigmoidoscopy done between 55 and 64 years old can offer an important reduction in CCR incidence and mortality.

cancer colon hereditary

The usual recommendation is for the test to be done every 5 years in conjunction with FOBT every 3 years Colonoscopy examines the whole colon and rectum.

A form of sedation is recommended for patient comfort. A more complex cleaning of the colon is needed before the investigation.

cancer colon hereditary

It has the advantage of biopsy, too. Death from CCR is reduced by about 70 percent. The usual recommendation of testing is at 10 years, as long as other tests are negative Double-contrast barium enema : less sensitive than colonoscopy for detecting small polyps and cancers; has an utility for those who cannot undergo colonoscopy.

New screening tests are under investigation: stool DNA testing trials showed a high rate of false positivesvirtual colonoscopy and capsule endoscopy; they should not yet be used for screening. Cancer colon hereditary had two arms: one used low dose helical CT and the other, standard chest X ray.

On average over the three rounds of screening exams, The results showed that using the CT screening t­here is a 15 to 20 percent lower risk of dying from lung can­cer when compared with chest X ray. The adenocarcinomas and squamous types were the most frequently detected, while small cell lung cancer, known for its agresivity, was infrequently found on either CT or chest X ray Mammography This screening test for breast cancer has been shown to reduce mortality from the disease in women aged 40 to 74, especially in those aged 50 or older.

To date, no differences are between classic film mammography and the digital one. Women with breast implants should continue to have mammograms. A special technique called implant displacement views may be used. Modern mammograms cancer colon hereditary a very small amount of radiation.

Usually, the risk of exposing to radiation is surpassed by the negi genitali of the test, but total dose of radiation after several tests must be kept in notice.

Prevenirea cancerului prin intermediul unor programe de screening

This test has the advantage of the possibility of being installed in mobile facilities. A new technique - 3D mammography tomosynthesis - has not been compared with 2D mammography in randomized studies, and cannot yet be recommended for screening purpose.

cancer colon hereditary

Pap test and Human Papilloma Virus HPV testing These tests reduce the incidence of cervical cancer because they allow abnormal cells to be identified and treated before they transform into cancer.

They also help reduce death from un medicament parazitar pentru întreaga familie disease.

cancer colon hereditary

It is generally recommended to begin at the age of 21 or 3 years after becoming sexually active and to end at the age of 65, as long as recent results have been normal. There are 12 high-risk HPV types, most cancers cancer colon hereditary linked to subtypes 16 and Although the infection is very common, vaccin papillomavirus enceinte most cases the immune system will suppress it in 1 to 2 years; but if the infections persists, the cellular changes can evolve to precancerous lesions, which finally turn into cancer.

The process can take from 10 to 20 years.

Genetic Counseling and Colorectal Cancer Risk hpv cause herpes

Results cancer colon hereditary Pap cancer colon hereditary are reported using the Bethesda System. If results show severe cancer colon hereditary, further tests apariția papiloamelor pe pleoape needed like colposcopy. A newer version of Pap test liquid based one offers the advantage of simultaneous testing for HPV from same specimen. It also reduces the possibility of unsatisfactory specimen and is considered similar to cytology based test in terms of detecting cellular abnormalities.

Women with certain risk factors may need to have more frequent screening or to continue screening beyond the age of These risk factors include being infected with the human immunodeficiency virus HIVbeing immunosuppressed, having been exposed to diethylstilbestrol before birth, and having been treated for a precancerous cervical lesion or cervical cancer. Women who have had a hysterectomy surgery to remove the uterus and cervix do not need to have cervical screening, unless the hysterectomy was done to treat a precancerous cervical lesion or cervical cancer.

For women aged 30 and older, Pap and HPV co-testing is less likely to miss an abnormality than Pap testing alone. A good option in this case, sustained by clinical trials, is to lengthen the screening interval to 5 years, still allowing the detection and treatment in time.

The ATHENA trial, which included 47, women, showed that HPV testing performed better than Pap testing at identifying women at risk of developing high risk cervical cell abnormalities. Other studies also confirm this hypothesis. The risk to develop cervical cancer after negative HPV test is extremely low.

cancer colon hereditary

The testing alone is regarded as a future direction in screening for cervical cancer, and is expected to be implemented soon in practice guidelines 15,16, Also, vaccines for HPV are giving good results and should be encouraged before becoming sexually active Other screening tests - can be used in certain high risk situations, in selected patients PSA test The test is often done in association with a digital rectal exam, and it was thought to be able to detect cancer at an early stage.

Expert groups no longer recommend routine testing for most men because trials have shown little to no effect on prostate cancer death and the screening can lead to overdiagnosis and overtreatment If a woman or her doctor notices a lump, un­usual discharge or other modification in the breast, it is important to have additional tests.

De ce testul Harmony? Testarea Harmony este un test screening, consultul genetic inainte si dupa obtinerea rezultatelor fiind obligatoriu.

The best moment for breast exam is 5 days after the end of the period. Other methods under evaluation are ultrasonographyCT scansPET scansscintimammographyelastographythermographyductal lavageand others which need to prove their benefit in trials.

The use of mammography is limited to advanced age, as there are evidence suggesting that BRCA carriers are more susceptible to breast cancer induction by X-ray damage It has not been shown to reduce deaths from cancer. Skin exams Regular examination of skin done by doctor or high risk skin cancer patient patients has not been proven to reduce the risk of dying by skin cancer and may lead to overtreatment.

Cauzele genetice ale infertilitatii feminine:

However, people should be aware of changes in their skin, such as the apparition of a new lesion or change in a existing one, and report it to cancer colon hereditary doctor. Alpha-fetoprotein blood test The test is used in selected, high-risk cases mostly patients with hepatitis B and C, heavy alcohol consumption, cirrhosis, exposure to aflatoxinsalong with liver ultrasound to try to find liver cancer in early stage. CA test The test is often done in association with transvaginal ultrasound, and has been tested to be included in screening especially for women with high risk of the disease.

It has not been shown to be an effective screening test. Its best use remains evaluating the recurrence in women previously diagnosed with the cancerous disease Although many methods of screening have been tested and several are still under evaluation, the ideal test for certain cancer sites is still waited for.

A great enthusiasm was seen initially with the apparition of tumor markers like PSA, CEA, CACA regarding their use in screening - unfortunately not confirmed by clinical trials.

The desiderate for an ideal tumor marker for every site, available for testing on blood samples of healthy persons, still remains an idea not yet feasible. Also, more precise, with low-radiation dose and accessible imagistic studies, that allow detection of cancer or its precursors in early stage, are urgently needed. That is why, using medically proven forms of primary prevention like education and vaccines and secondary prevention screeningin well organized national health strategies, along with investigating new accessible methods for testing, should be our major interest and concern.

Vreau mai multe informatii

Maximising benefit and minimising harm of screening. BMJ Clinical research ed. Miron L. Terapia cancerului: opţiuni bazate pe dovezi, Editura Institutul European, Iaşi American Cancer Society.

Genetic Counseling and Colorectal Cancer Risk papilomatosis genital tratamiento Prevenirea cancerului prin intermediul unor programe de screening Familial cancer causes. Lefter1, V.

Atlanta: American Cancer Society; Preventive Services Task Force. Screening for colorectal cancer: U. Preventive Services Task Force recommendation statement. Annals of  Internal Medicine ; 9 Diagnostic accuracy of faecal occult blood tests used in screening for colorectal cancer: A systematic review.

Journal of Medical Screening ; 14 3 Noninvasive testing for colorectal cancer: A review. American Journal of Gastroenterology ; 6 Once-only flexible sigmoidoscopy screening in prevention of colorectal cancer: a multicentre randomised controlled trial.

Open in a separate window Hypopharynx cancer usually occurs in the second half of life, between 50—79 years, more frequent in males.

Lancet ; Ransohoff DF. How much does colonoscopy reduce colon cancer mortality? Exit Disclaimer Annals of Internal Medicine Online June 29, Effects of mammography screening under different screening schedules: model estimates of potential benefits and harms.

LABORATOARELE GENETIC CENTER | Regina Maria

Annals of Internal Medicine ; 10 Diagnostic performance of digital versus film mammography for breast-cancer screening. New England Journal of Medicine ; 17 Cervical cancer risk for women undergoing concurrent testing for human papillomavirus and cervical cytology: A population-based study in routine clinical practice. Lancet Oncology ; 12 7 Moyer VA, on behalf of the U. Screening for Cervical Cancer: U. Annals of Internal Medicine ; 12 American Cancer Society, American Society for Colposcopy and Cervical Pathology, and American Society for Clinical Pathology screening guidelines for the prevention and early detection of cervical cancer.

Ablin RJ. The great prostate mistake ; Updated 9 March. Morris, Joi L. Amherst, N. Pijpe, A.