Breast cancer – information, symptoms and treatments
What is Breast Cancer?
The term breast cancer refers to a malignant tumor that has developed from cells in the breast. The breast is composed of two main types of tissues: glandular tissues and stromal (supporting) tissues. Glandular tissues house the milk-producing glands (lobules) and the ducts (the milk passages) while stromal tissues include fatty and fibrous connective tissues of the breast. The breast is also made up of lymphatic tissue-immune system tissue that removes cellular fluids and waste….
Symptoms of Breast Cancer
Early breast cancer usually does not cause pain. In fact, when it first develops, breast cancer may cause no symptoms at all…
But as the cancer grows, it can cause these changes:
1. A lump or thickening in the breast or armpit.
2. A change in the size or shape of the breast.
3. Discharge from the nipple.
4. A change in the color or texture of the skin of the breast or areola (such as dimpling, puckering, or scaliness)…
Treatment of a Breast Cancer in India
Mastectomy in India Mastectomy is the surgical removal of a breast. Surgery is presently the most common treatment for breast cancer. Following mastectomy, immediate or delayed breast reconstruction is possible in many instances..
Axillary Node Dissection in India
Axillary node dissection, the surgical removal of the axillary (armpit) lymph nodes, is usually performed on patients with invasive cancers. A radical mastectomy, modified radical mastectomy, or lumpectomy operation often includes axillary node dissection (this involves a separate incision for lumpectomy patients). After surgery, the axillary lymph nodes are examined under a microscope to determine whether the cancer has spread past the breast and to evaluate treatment options….
Sentinel Lymph Node Biopsy in India
Sentinel lymph node biopsy is a new procedure that involves removing only one to three sentinel lymph nodes (the first nodes in the lymphatic chain). To perform sentinel node biopsy, a radioactive tracer and/or blue dye is injected into a region of a tumor. The dye is then carried to the sentinel node (the lymph node most likely to be cancerous if the disease has spread from its original origin)…..
Lumpectomy in India
Lumpectomy is the surgical removal of a cancerous lump (or tumor) in the breast, along with a small margin of the surrounding normal breast tissue. Lumpectomy may also be called wide excision biopsy, breast conserving therapy or quadrantectomy (this latter term is used when up to one fourth of the breast is removed)….
Chemotherapy in India
it is important to note that the majority of the side effects associated with chemotherapy are temporary and only occur during or immediately after treatment. In the vast majority of cases, the benefits of treating cancer with chemotherapy far outweighs the risks or inconveniences of any side effects. Chemotherapy is only one possible treatment for breast cancer and may be used in addition to surgery or other treatments. Patients should discuss all aspects of chemotherapy and breast cancer treatment with their physician or cancer treatment team…
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Genetic Causes Of Melanoma
Early signs of melanoma are changes to the shape or color of existing moles. The mole may itch, ulcerate or bleed. Metastatic melanoma may cause general symptoms like loss of appetite, nausea, vomiting and fatigue. Metastasis as the first symptom of melanoma is possible; however, fortunately less than a fifth of melanomas diagnosed early become metastatic.
Familial melanoma is genetically heterogeneous, and loci for familial melanoma have been identified on the chromosome arms 1p, 9p and 12q. Multiple genetic events have been related to the pathogenesis of melanoma. The multiple tumor suppressor 1 (CDKN2A/MTS1) gene encodes p16INK4a — a low-molecular weight protein inhibitor of cyclin-dependent protein kinases (CDKs) — which has been localised to the p21 region of human chromosome 9.
Today, melanomas are diagnosed only after they become visible on the skin. In the future, however, physicians will hopefully be able detect melanomas based on a patient’s genotype, not just his or her phenotype. Recent genetic advances promise to help doctors to identify people with high-risk genotypes and to determine which of a person’s lesions have the greatest chance of becoming cancerous.
A number of rare mutations, which often run in families, are known to greatly increase one’s susceptibility to melanoma. One class of mutations affects the gene CDKN2A. An alternative reading frame mutation in this gene leads to the destabilization of p53, a transcription factor involved in apoptosis and in fifty percent of human cancers.
Another mutation in the same gene results in a non-functional inhibitor of CDK4, a cyclin-dependent kinase that promotes cell division. Mutations that cause the skin condition Xeroderma Pigmentosum (XP) also seriously predispose one to melanoma. Scattered throughout the genome, these mutations reduce a cell’s ability to repair DNA. Both CDKN2A and XP mutations are highly penetrant.
Other mutations confer lower risk but are more prevalent in the population. People with mutations in the MC1R gene, for example, are two to four times more likely to develop melanoma than those with two wild-type copies of the gene. MC1R mutations are very common; in fact, all people with red hair have a mutated copy of the gene.
Two-gene models of melanoma risk have already been created, and in the future, researchers hope to create genome-scale models that will allow them to predict a patient’s risk of developing melanoma based on his or her genotype. In addition to identifying high-risk patients, researchers also want to identify high-risk lesions within a given patient.
Many new technologies, such as optical coherence tomography (OCT), are being developed to accomplish this. OCT allows pathologists to view 3-D reconstructions of the skin and offers more resolution than past techniques could provide. In vivo confocal microscopy and fluorescently tagged antibodies are also proving to be valuable diagnostic tools. Mutation of the MDM2 SNP309 gene is associated with increased risk of melanoma in younger women.
Most of the treatments require multiple visits to the doctor. Laser and electrocautery treatments are not always effective because they only reach the outermost layers of the skin, while moles penetrate very deep into the dermal tissue, often beyond the reach of these treatments. Surgery, the other option doctors commonly offer, involves cutting out the mole. The resulting wound requires stitches, which will in turn leave a scar.
NeviCurative is a powerful all natural topical treatment proven to eliminate and defeat moles or nevi. Recent clinical trials have established the ability of the active constituents in NeviCurative to effectively eradicate skin moles and impair the growth of human melanoma cells. NeviCurative has therefore been shown to eliminate even the most stubborn moles, regardless of their location on the body, even when other treatments have failed.
NeviCurative is well-known for its antioxidant properties. It is comprised of certified organic medicinal plant extracts, which have demonstrated their ability to eradicate melanomas and skin tumors in laboratory tests. These extracts have a remarkable array of pharmacological and biochemical properties, which are highly effective in eradicating moles.
The pharmacological strength of NeviCurative provides effective elimination of moles without scarring, tissue damage, or recurrence. The treatment is painless and delivers profound results in the elimination of moles, returning skin tissue back to its original state. To learn more, please go to http://www.bcured.net.
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