Please enable JavaScript.
Coggle requires JavaScript to display documents.
Srgery - Coggle Diagram
Srgery
-
- Properties that allow metastasis
- General Description: To metastasize successfully, cancer cells have to detach from their original location, invade a blood or lymphatic vessel, travel in the circulation to a distant site and establish a new cellular colony. At every one of these steps, they must escape many controls that, in effect, keep normal cells in place.
- Specific Cancer Cell Abilities: Cancer cells have the following abilities that allow metastases:
- Defective cell adhesion: Malignant cells lack adhesion proteins that bind the cells to each other, following tissues. They are, therefore, free to detach and migrate.
- Tumour angiogenesis: Allows proximity of malignant cells to the newly formed capillaries and so enhances easy access to the circulation.
- Production of proteolytic enzymes: That digest the basement membrane allowing invasive, and digest capillary and lymphatic wall to allow them access to the lumen.
- They escape apoptosis: When they reach some tissue different from their origin.
-
- Local spread: First into the tissues of the same organ, then into neighbouring organs.
- Lymphatic spread: Malignant cells very frequently invade the endothelium of the lymphatic capillaries and then either grow inside the lymphatic vessels (permeation) or are carried as emboli to the draining lymph nodes (embolization). The cells may then be carried to the afferent lymphatics to the next group of lymph nodes. Obstruction of lymph nodes may lead to oedema in the drainage area and also in reversal of lymph flow.
- Blood-borne spread: Malignant cells can also invade walls of thin capillaries, and, thence, tumour emboli are carried to distant organs leading to micro metastases, which may remain silent for a long time or grow leading to gross distant deposits, in the lung, liver, bones, and brain.
- Additional Note: Fortunately, even when cancer cells do get into the circulation, the formation of secondary tumours is not inevitable. Probably fewer than one in 10,000 of the cancer cells that reach the circulation survive to establish a new tumour at a distant site. Blood circulation explains much about why various metastatic cancers spread preferentially to certain tissues. Circulating tumour cells usually get trapped in the first vascular bed (a network of capillaries) that they encounter ("downstream" of their origin). The first vascular bed encountered by blood leaving most organs is in the lungs. Only the gastrointestinal tract sends its blood to the liver first through the portal vein. Accordingly, the lungs are the most common site of metastasis, followed by the liver. The latter is the commonest site of deposits from the gut.
- Transcoelomic spread: Malignant cells travel along cavities. An example is the spread of carcinoma of the stomach, through the peritoneal cavity, down to the ovaries.
- Stepwise versus explosion concept of metastasis
- Formerly, it was thought that malignant dissemination takes place at two steps, the first is lymphatic, and the second is blood-borne.
- This concept is no longer acceptable, and we now know that even at the earliest stage tumour cells invade both the lymphatics and the blood vessels simultaneously.
- In other words, as the tumour spreads it not just explodes in all directions. Regional lymph node involvement is no longer regarded as a stage in the progression of the disease but as an involvement that widespread dissemination has occurred.
-
Staging is an expression of the extent of malignancy and, hence, reflects the likely prognosis. The most widely used staging system is the TM in which the three components of the disease are assessed. These are
• Extent of primary tumour (T), i.e., its size, and mobility.
• Presence or absence, and extent of lymph node involvement (N).
-
-
-
-
تمام، فهمت. سأقوم بتنظيم محتوى آخر صفحتين فقط التي أرفقتها (الخاصة بـ "Treatment") في شكل خريطة ذهنية (Mind Map) باللغة الإنجليزية، مع الحفاظ على كل كلمة موجودة في النص الأصلي.
-
-
Main Branch 1: Diagnosis
- Early detection of asymptomatic cases (screening)
- Some people may have a higher risk of developing certain malignant tumours. In this case it is sensible to follow certain screening programs to detect the neoplasm as early as possible. Common examples are:
- Annual soft tissue mammography for females who have a higher chance of developing breast cancer. These include patients who already had carcinoma of the breast on one side, the incidentally relatives of patients with breast carcinoma, or patients who had excision of benign dysplastic lesions.
- Annual colonoscopy for patients with ulcerative colitis who have a high risk of developing colorectal cancer. These are patients with pancolitis of more than ten-year duration.
- Annual prostate specific antigen (PSA) for men above fifty.
- Diagnosis of symptomatic cases
- The aim is to diagnose the disease and to determine its extent (stage). In addition to thorough clinical assessment, the following diagnostic aids are commonly used:
- Radiological: Various radiological techniques including contrast studies, ultrasound, CT (Fig. 10.7) and MRI are utilized for diagnosis.
- Endoscopy: This is very useful for diagnosis of most lesions of the respiratory, gastrointestinal and urinary systems. Bronchoscope, gastroscope (EGS) incorporates an U/S probe into the endoscope. Excellent cut display of the depth of tumour invasion can be achieved of the cancers of the esophagus, stomach, pancreas and rectum.
- Tissue biopsy, tru-cut needle, endoscopic or operative biopsies obtain a piece of tissue from which sections are made for histological examination. Diagnosis of malignancy depends on cellular morphology as well as architectural disruption. The latter is the specific feature of malignancy. Histopathological findings are the most dependable.
- Cytology: The loss of cellular adhesion that is characteristic of malignancy allows easy retrieval of cells either by a fine needle aspiration or by a brush from surface lesions. Fine needle aspiration cytology is commonly used for diagnosis of the thyroid, breast, liver or prostate. Ultrasound or CT guidance of the needle allows accurate sampling of the suspicious area. Diagnosis depends on cellular morphology only, as the only cells and not tissues under the microscope. The test, therefore, requires an expert cytologist.
- Tumour markers are substances that are produced by cancer or by other cells of the body in response to cancer. Most tumour markers are made by normal cells as well as by cancer cells. However, they are produced in much higher levels in cancerous conditions. These substances can be found in the blood, urine, stool, tumour tissue, or other tissues or body fluids of some patients with cancer. Most tumour markers are proteins. However, with recent advances of gene expression and changes to DNA have also begun to be used as tumour markers.
- Tumour markers may to diagnose some types of cancer, monitor the effect of treatment, and detect a recurrence. Although an elevated level of a tumour marker may suggest the presence of cancer, this alone is not enough to diagnose it. Therefore, tumour markers are usually used in with other tests, such as imaging and biopsy, to diagnose cancer. Fig. 10.8 illustrates some of the common tumour markers.
- Isotopic scanning as positron emission tomography (PET): Utilizes a fluorine tagged tracer as flouro-desoxy-glucose for a functional scan detecting tumours with high glucose metabolism. It is sensitive for the detection of small metastases. Anatomical sites of such metastases can be more accurately determined if combined with a CT scan (PET-CT). Together with laparoscopy, both are the only two means available, so far, for the detection of peritoneal nodules or small liver metastases.
-