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Cervical tumor Cervical intraepithelial neoplasia(CIN) Introduction A group of precancerous lesion closely associated with the cervical cancer,which reflect the continuous process of the development of the cervical cancer. 1.CIN caused by virus infection rarely develop cervical cancer 2.CIN caused by multifactors may develop cervical cancer. 3.TBS diagnosing system by NCI (1).atypical squamous cells,ABC. (2).low-grade squamous intraepithelial lesion,LSIL. (3).high-grade squamous intraepithelial lesion ,HSIL. LSIL means CIN I,rarely develop cervical cancer. HSIL menas CIN II and III,may develop cervical cancer. Etiology HPV(human papillomaviruses) infection Epidemiologic risk factors for CIN: 1,multiple sexual partners 2,high-risk sexual partner 3,early onset of sexual activity(<16) 4,a history of STDs(especially, HPV infection) 5,cigarette smoking 6,immunodeficiency 7,long-tem oral contraceptive pill use Cervical Histological Specialty (i).primal squamo-columnar junction (ii).physiologic squamo-columnar junction (iii).transformation zone (iv).squamous metaplasia (v).squamous epithelization Pathology Cervical intraepithelial neoplasia(CIN) degree I: ie,mild dysplasia, heterotype cells occupy lower 1/3 layer degree II: ie,moderate dysplasia, heterotype cells occupy the lower 2/3 layer degree III: ie,severe dysplasia and carcinoma in situ, heterotype cells occupy whole layer Clinical findings Usually no symptoms or signs Early detection is extremely important Diagnosis Repeated cervical ctyology --TCT Colposcopic examination Biopsy—the most reliable method to make diagnosis 诊断:CIN I级 诊断:CIN I级 诊断:CIN II级 诊断:CIN II级 诊断:宫颈原位癌 诊断:宫颈原位癌 Treatment CINI:Cryotherapy can be used in small,limited lesions, with an effective rate of 95%.For lesions involving vagina or glands ,laser ablation is used with an effective rate of 93%. CINII:Cryotherapy(94% effective rate),laser ablation(92% effective rate) or cone excision can be used according to the range of lesion CINIII:Hysterectomy is recommended. Cone excision is used in young patients when infertility is desired. Cervical cancer Introduction The most common gynecologic cancers Usually occurs between 35~39 and 60~64.The average age at diagnosis of patients with cervical cancer is 52.2 years old. Etiology i.early marriage,early sexual activity and delivery, deranged sexual activity,poor economy and multipara ii.the women who has sexual activity with highrisk man iii.virus infection through sexual activity,such as herpes simplex virus II type,human papilloma virus and cytomegalovirus Histological genesis and development Most cervical cancer occurs on the transformation zone. Unmature metaplastic squamous cells metabolize actively,and may develop cervical cancer under the stimuLation of some factor Pathology I .squamous carcinoma: account for 80%~85% of cervical cancer (1)macro examination: There is no obvious difference among CIN,microscopic invasive cancer and early stage of invasive cancer (a).exogenic cancer:the most common type (b).endogenous cancer (c).ulcer type cancer (d).cervical canal type cancer (2)microscopic examination (a).microscopic invasive cancer: tear-drop or serrate cancer cell group growing through basal membrane (b).invasive cervical cancer: invasiveness of stroma is beyond the microscopic invasive cancer,and according to the cellular differentiation it is divided into 3 degrees: degree I:cornified large cell type,mitosis<2/HP degree II:uncornified large cell type,mitosis 2~4/HP degree III:small cell type,mitosis>4/HP 2 .adenocarcinoma :account for 15% of cervical Ca. (1).macro examination: originate from cervical canal, invade canal wall and paracervical tissue,protrude the external OS,focus appearance,cervical appearance (2).microscopic examination (a).mucous adenocarcinoma: origination,polyp protruding in gland cavity,stratified epithelium, nuclear atypia and mitosis is obvious (b).malignant cervical adenoma: also called microdeviation adenocarcinoma,tumor cell,gland,tumor epiderm, deeply invasion (c).squamoadenocarcinoma:origination,resulting from, close combination,transformation Metastatic path i. direct spreading: the most common way,exogenic type,cervical canal type ii. lymphatic metastasis: tumor embolus in lymphatic space,the first group of LN,the second group of LN iii. blood metastasis: extremely less Clinical stage:adopting FIGO(2000) stage Stage I cancer focus is located in the cervix Ia invasiveness can only be seen under microscope ,the depth of stroma invading≤5mm,width ≤ 7mm Ia1 the depth of stroma invading ≤ 3mm,,width≤7mm Ia2 the depth of stroma invading >3mm, ≤5mm ,width ≤ 7mm Ib clinically seen cancer focus is located in the cervix, superficial invasive cancer can be seen,preclinical focus range is beyond the stage Ia Ib1 clinical cancer volume ≤ 4cm Ib2 clinical cancer volume>4cm Stage II cancer focus is beyond cervix but not reach pelvic wall,involving vagina but not reach the low 1/3 IIa cancer chiefly spread to vagina, no obvious paracervical infiltration IIb cancer chiefly spread to paracervical tissue , Stage III cancer focus reach low 1/3 of vagina and /or pelvic wall, there may be hydronephrosis or unfunctional kidney IIIa chiefly spread to vagina and reach low 1/3 IIIb chiefly spread to paracervical tissue and reach pelvic wall or there is hydronephrosis or unfunctional kidney Stage IV the cancer spread beyond the true pelvis or infiltrate the mucosa of rectum or bladder IVa infiltrating the mucosa of rectum or bladder IVb spreading beyond the true pelvis Clinical manifestation symptoms:at early stage,cervical canal cancer (i).vaginal bleeding: young patients manifest contacting bleeding, senile patient, exogenic cancer,endogenous cancer (ii).vaginal discharge: white or bloody discharge,purulent or ricewater-like discharge (iii).symptoms of late stage cancer: depending upon the infiltrating range,in severe case,at end stage Clinical manifestation body signs (i).at CIN,microinvasive and early invasive cancer (ii).with the further development of invasive cancer there will be i).exogenic type, ii)endogenous type, iii)late stage, iv)neighbor infiltration Diagnosis i.cervical smear for cytologic examination ii.iodine test iii.nitrogen molecular laser tumor intrinsic fluorescence iv.colposcopy v.biopsy of cervix and cervical canal:the most reliable method to make diagnosis vi.cervical conization Differential diagnosis cervical erosion, cervical polyp, cervical TB, cervical papilloma endometriosis Management (i).surgical treatment:indication Ia~Ⅱb early stage Ia1: total hysterectomy, If ovary is normal, ovary should be reserved. Ia2-Ⅱb (early stage) : radical hysterectomy with pelvic lymphadenectomy, If ovary is normal, ovary should be reserved. (ii).radiotherapy: intracavity irradiation , extrinsic irradiation Indication: Ⅱb late stage, III, IV; can not endure operation Management (iii).comprehensive treatment of operation and radiotherapy: Preoperation radiation:locally advanced cervical cancer Postoperation radiation:If there is lymph nodes , or parametrail involvement (iv).chemotherapy: Indication: late stage or recurrent cervical cancer, Prognosis 1. 2. 3. 4. associated with clinical stage, pathologic type and treating method. chief cause of death at late stage Uremia Hemorrhage Infection Cachexia Prophylaxis I popularization of cancer prevention knowledge, sugesting late marriage,less birth and sexual health education II.the screening and mass treatment of cervical cancer should be made regularly III.treating moderate and severe cervical erosion actively,CIN should be diagnosis and treated early to stop the development of cervical cancer Follow up The first follow up is in 1 month after discharge,then once a time every 2~3 month within 1 year.in the second year once a time every 3~6 month.during 3~5 years after discharge once a time each year,The contents of the follow up include clinical examination,regular chest X-ray and blood RT