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Cancer of the cervix is the most common female genital cancer in developing countries every year about 500,000 women , acquire the disease and 75% are from frame developing countries. About 300,000 women also die from the disease annually and of these 75% are from developing countries Finland which has an advanced population based screening program has one of the lowest rates in the world. 4-6 % of female genital cancers. 40-50 years old Risk factors and aetiology Coitus at at young young age: age: <16 Coitus <16years yearsold oldincreased increasedrisk riskby by50% 50% Number of sexual sexual partners: 66 sexual Number of sexual partners partners or or more more increase increaserisk riskby by 14.2 folds. 14.2 folds. Smoking Smoking Smoking 1212 years increase thethe riskrisk by by 12.7 folds. Smokingfor> for> years increase 12.7 folds. Male related related risk risk factors: factors: Male number the partners previous relationships numberofof the partners previoussexual sexual relationshipsisisrelevant relevant. . cervical risk if if partners has penile cancer cervicalcancer cancer riskincreased increased partners has penile cancer (circumcision) (circumcision) Previous Previouswife wifewith withcervical cervicalcancer. cancer. Previous CIN CIN Previous Poor uptake of of screening program. program. Poor uptake Long term term use of the Long the contraceptive contraceptive pill pill increase the risk risk due to increasing increasing exposure to seminal fluids. fluids. Barrier method decrease the Barrier method the risk risk (condan) (condan) Immuno suppresion suppresion risk riskincreased increasedwith withimmuno immunosuppressed suppressedrenal renal Immuno transplant in HIV HIVpositive positivewomen. women. transplant patients and in HPV (Human (Humanpapilloma papillomavirus virus) infection ) infectionmainly mainly 16,18 HPV 16,18 thethe main aetiological is infection with subtypes of of HPV main aetiological is infection with subtypes HPV(16,18) (16,18) Low socioecomic socioecomic class class of Low HPV 16,18 Smoking Cervical cell Male factors Infhibation of CX cellp53 tumour suppression gyne Protection against tumour development lifted Cancer develops Multiparous. Low socioeconomic class. Poor hygiene. Prostitutes. Low incidence in Muslims and Jews. Cervical dysplasia. (Cervical intraepithelial neoplasia) CIN III / CARCINOMA IN SITU THE LESION PROCEEDS THE INVASION BY 10-12 YEARS Early symptoms - None. - Thin, watery, blood tinged vaginal discharge frequently goes unrecognized by the patient. - Abnormal vaginal bleeding Intermenstrual Postcoital Perimenopausal Postmenopausal - Blood stained foul vaginal discharge. Late symptoms - Pain, leg oedema. Urinary and symptoms dysuria haematuria rectal bleeding constipation haemorrhoids - Uraemia rectal Squamous cell carcinoma- 90%. Adenocarcinoma- 10%. Exophytic: is like cauliflower filling up the vaginal vualt. Endophytic: it appears as hard mass with a good deal of induration. Ulcerative: an ulcer in the cervix. 1- History. Many women are a symptomatic . Presented with abnormal routine cx smear Complain of abnormal vaginal bleeding I M bleeding post coital bleeding perimenopausal bleeding postmenopausal bleeding blood stain vaginal discharge 2- Examination: Mainly vaginal examination using cuscu’s speculem nothing is found in early stage . Mass ,ulcerating fungating in the cervix P/V P/R is very helful. Cytology Histology calposcopy o o o o o o o o o o o Review her history. General examination: Anaemia. Lymphadenopathy-Supraclavicular LN. Renal area. Liver or any palpable mass. Oedema. Laboratory tests: CBC, LFT, RFT, Urine analysis. Tumour markers. Chest X- ray, abdominal X- ray, IVU. CAT, MRI, if necessary. Ultrasound. Lymphography, if necessary. Best to follow FIGO system. Examination under anaesthesia. Bimanual palpation. P/V, P/R. Cervical biopsy, uterine biopsy. Cystoscopy, Proctoscopy, if necessary. Once cancer cervix is found (diagnosed), more tests will be done to find out if the cancer cells have spread to other parts of the body. This testing is called staging. TO PLAN TREATMENT, A DOCTOR NEEDS TO KNOW THE STAGE OF THE DISEASE. Direct Lymphatic Dissemination (late) - A- primary node: parametrial. Paracervical. Vesicovaginal. Rectovaginal. Hypogastric. Obturator and external iliac - parametrial spread causes obstruction of the ureters, many deaths occur due to uraemia. - Obstruction to the cervical canal results in pyometria. Uteruq. Vagina. Parametrium. Bladder and rectum. B-Secondary nodes: Common iliac Sacral Vaginal Paraaortic Inguinal. Cervical ectropion. Cervical tuberculosis. Cervical syphilis, Schistosomiasis, and Choriocarcinoma are rare causes. Surgical. Radiotherapy. Radiotherapy & Surgery. Radiotherapy and Chemotherapy followed by Surgery. Palliative treatment. Fitness of the patients Age of the patients Stage of disease. Type of lesion Experience and the resources avalible. The classic surgical procedure is the wertheim’s hystrectomy for stage Ib,IIa, and some cases of IIb in young and fat patient Total abdominal hystrectomy including the parametrium. Pelvic lymphadenectomy 3 cm vaginal cuff The original operation conserved the ovaries ,since squamouss cell carcinoma does not spread dirctly to the ovaries. Oophorectomy should be performed in cases of adenocarcinoma as there is 5-10% of ovarian metastosis It allows presentation of the ovaries (radiotherapy will destroythem). There is better chance of preserving sexual function. (vaginal stonosis occur in up 85% of irradiates. Psychological feeling of removing the disease from the body . More accute staging and prognsis Haemorrhage: primary or secondary. Injury to the bladder, uerters. Bladder dysfunction. Fistula. Lymphocele. Shortening of the vagina. INDICATIONS OF P/O XRT FOLLOWING WERTHEIM’S HYSTERECTOMY (STAGE I , IIa): Positive pelvic lymph nodes. Tumour close to resection margins and/or parametrial extension. Stage IIb and III Radical Radiotherapy External irradiation (Teletherapy). Intracavitary radiation (Brachytherapy). In some cases of stage IIa or b radio and chemotherapy to be given then followed by simple hysterectomy ------- For stage IV – individualized therapy. Some suitable for palliative XRT ( usually intracavitary Caesium). Some suitable for extensive surgery. Some suitable for chemotherapy. Good nursing care. Analgesia-must be used in sufficient amount to ----- pain (Codein sulfate, Pethidine, Morphine, Diamorphine). Antiemetic if necessary. IV drip, entral, and parentral feeding. Urinary Catheterization. Other measures for symptom relief. Depends on: Age of the patient. Fitness of the patient. Stage of the disease. Type of the tumour. Adequacy of treatment. THE OVERALL 5 YEARS SURVIVAL FOLLOWING THERAPY: Stage I -------80% Stage II-------50-60% Stage III-------30-40% Stage IV-------4% 1. Local recurrence: Radiation – if not used. Pelvic exenturation. 2. Distant disease Chemotherapy. On completion of treatment all patients are given a vaginal dilator to use until vaginal mucosa healed, this prevents vaginal stenosis. Premenopausal patients commenced on HRT: post hysterectomy-Extraderm skin patches 50 meg twice weekly. No hysterectomy- Cycloprogyn 1mg daily. The patient to be seen 1/12 post-treatment. 3 monthly for 2 years. 4 monthly for 3rd year. 6 monthly until 5years. Then yearly all her life. Patients with stage I and II disease treated with radical radiotherapy will be assessed by EUA approximately 3 months after completing treatment. Cancer of the cervix is still quite common, reduction in incidence depends on the quality of the screening program. The aetiology appears to be multifactorial the prime oncogenic agent is probably [HPV16,18]. Clinical presentation is with inermenstrul,postcoital, postmenospausal bleeding or following abnormal cytology. Tumour spreads locally to involve the uterus bladder , vagina, parametrium, ureters, rectum and bone. Spread also to the internal and external iliac , obdurater and common iliac nodes then to para- aortic nodes. Blood borne metastasis spread to liver, lung and bone occur . Microinvasion squamous tumour carry a good prognosis allowing conservative treatment initially if required. Early invasive squamous cell disease (stage Ib,IIa and in some cases of IIb) may be treated by either a wertheimes hysterectomy or radiotherapy as first line treatment. Advanced stage (IIb, III,IV) treated by radio or chemotherapy. Glandular tumours (adenocarcinomas) are not detectable by screening are associated with skip lesions and require radical surgery.