Colposcopy of the Uterine Cervix
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Reference Sheet 1
MALE SEXUAL SYSTEM 8 7 8 OJ 7 .£l"00\.....• ;:; ::>0\~ <Il '"~IQ)I"->. ~cru::>s ~ 6 5 bladder penis prostate gland 4 scrotum seminal vesicle testicle urethra vas deferens FEMALE SEXUAL SYSTEM 2 1 8 " \ 5 ... - ... j 4 labia \ ""\ bladderFallopian"k. "'"f"";".'''¥'&.tube\'WIT / I cervixt r r' \ \ clitorisurethrauterus 7 \ ~~ ;~f4f~ ~:iJ 3 ovaryvagina / ~ 2 / \ \\"- 9 6 adapted from F.L.A.S.H. Reproductive System Reference Sheet 3: GLOSSARY Anus – The opening in the buttocks from which bowel movements come when a person goes to the bathroom. It is part of the digestive system; it gets rid of body wastes. Buttocks – The medical word for a person’s “bottom” or “rear end.” Cervix – The opening of the uterus into the vagina. Circumcision – An operation to remove the foreskin from the penis. Cowper’s Glands – Glands on either side of the urethra that make a discharge which lines the urethra when a man gets an erection, making it less acid-like to protect the sperm. Clitoris – The part of the female genitals that’s full of nerves and becomes erect. It has a glans and a shaft like the penis, but only its glans is on the out side of the body, and it’s much smaller. Discharge – Liquid. Urine and semen are kinds of discharge, but the word is usually used to describe either the normal wetness of the vagina or the abnormal wetness that may come from an infection in the penis or vagina. Duct – Tube, the fallopian tubes may be called oviducts, because they are the path for an ovum. -
Analysis of Conization Results in Patients
Published online: 2020-05-29 THIEME 266 Original Article Analysis of Conization Results in Patients undergoing Hysterectomy for Uterine Adenocarcinoma Análise dos resultados de conização nos pacientes submetidos a histerectomia por adenocarcinoma uterino Denise Gasparetti Drumond1 Isabel Cristina Gonçalves Leite1 Vivian de Oliveira Rodrigues1 Gabriel Duque Pannain1 Miralva Aurora Galvão Carvalho1 Renata Guimarães Rabelo do Amaral1 1 Department of Surgery, Universidade Federal de Juiz de Fora, Juiz de Address for correspondence Denise Gasparetti Drumond, MD, Fora, MG, Brazil Universidade Federal de Juiz de Fora, Juiz de Fora, MG, 36036-900, Brazil (e-mail: [email protected]). Rev Bras Ginecol Obstet 2020;42(5):266–271. Abstract Objective To observe if the histopathological result of a conization performed after cervical adenocarcinoma in situ diagnosis is compatible with the histopathological analysis of a subsequent hysterectomy. Methods The present descriptive and observational research consisted of the analysis of the medical records of 42 patients who were diagnosed with in situ adenocarcinoma postconization. The analysis consisted of whether there was compatibility between the histopathological reports of conization and hysterectomy and if there was an associa- tion between adenocarcinoma in situ and another neoplasia (squamous disease). Interpretation of any immunohistochemistry reports obtained was also performed. In addition, clinical and epidemiological data were also analyzed. Results A total of 42 conizations were performed, 33 (79%) were cold knife coniza- tions and 9 (21%) were loop electrosurgical excision procedures (LEEPs). Of the patients analyzed, 5 (10%) chose not to undergo subsequent hysterectomy to preserve fertility or were < 25 years old. Out of the 37 patients with adenocarcinoma in situ who underwent subsequent hysterectomy, 6 (16%) presented with residual disease. -
Ovarian Cancer and Cervical Cancer
What Every Woman Should Know About Gynecologic Cancer R. Kevin Reynolds, MD The George W. Morley Professor & Chief, Division of Gyn Oncology University of Michigan Ann Arbor, MI What is gynecologic cancer? Cancer is a disease where cells grow and spread without control. Gynecologic cancers begin in the female reproductive organs. The most common gynecologic cancers are endometrial cancer, ovarian cancer and cervical cancer. Less common gynecologic cancers involve vulva, Fallopian tube, uterine wall (sarcoma), vagina, and placenta (pregnancy tissue: molar pregnancy). Ovary Uterus Endometrium Cervix Vagina Vulva What causes endometrial cancer? Endometrial cancer is the most common gynecologic cancer: one out of every 40 women will develop endometrial cancer. It is caused by too much estrogen, a hormone normally present in women. The most common cause of the excess estrogen is being overweight: fat cells actually produce estrogen. Another cause of excess estrogen is medication such as tamoxifen (often prescribed for breast cancer treatment) or some forms of prescribed estrogen hormone therapy (unopposed estrogen). How is endometrial cancer detected? Almost all endometrial cancer is detected when a woman notices vaginal bleeding after her menopause or irregular bleeding before her menopause. If bleeding occurs, a woman should contact her doctor so that appropriate testing can be performed. This usually includes an endometrial biopsy, a brief, slightly crampy test, performed in the office. Fortunately, most endometrial cancers are detected before spread to other parts of the body occurs Is endometrial cancer treatable? Yes! Most women with endometrial cancer will undergo surgery including hysterectomy (removal of the uterus) in addition to removal of ovaries and lymph nodes. -
Updates in Uterine and Vulvar Cancer
Management of GYN Malignancies Junzo Chino MD Duke Cancer Center ASTRO Refresher 2015 Disclosures • None Learning Objectives • Review the diagnosis, workup, and management of: – Cervical Cancers – Uterine Cancers – Vulvar Cancers Cervical Cancer Cervical Cancer • 3rd most common malignancy in the World • 2nd most common malignancy in women • The Leading cause of cancer deaths in women for the developing world • In the US however… – 12th most common malignancy in women – Underserved populations disproportionately affected > 6 million lives saved by the Pap Test “Diagnosis of Uterine Cancer by the Vaginal Smear” Published Pap Test • Start screening within 3 years of onset of sexual activity, or at age 21 • Annual testing till age 30 • If no history of abnormal paps, risk factors, reduce screening to Q2-3 years. • Stop at 65-70 years • 5-7% of all pap tests are abnormal – Majority are ASCUS Pap-test Interpretation • ASCUS or LSIL –> reflex HPV -> If HPV + then Colposcopy, If – Repeat in 1 year • HSIL -> Colposcopy • Cannot diagnose cancer on Pap test alone CIN • CIN 1 – low grade dysplasia confined to the basal 1/3 of epithelium – HPV negative: repeat cytology at 12 months – HPV positive: Colposcopy • CIN 2-3 – 2/3 or greater of the epithelial thickness – Cold Knife Cone or LEEP • CIS – full thickness involvement. – Cold Knife Cone or LEEP Epidemiology • 12,900 women expected to be diagnosed in 2015 – 4,100 deaths due to disease • Median Age at diagnosis 48 years Cancer Statistics, ACS 2015 Risk Factors: Cervical Cancer • Early onset sexual activity • Multiple sexual partners • Hx of STDs • Multiple pregnancy • Immune suppression (s/p transplant, HIV) • Tobacco HPV • The human papilloma virus is a double stranded DNA virus • The most common oncogenic strains are 16, 18, 31, 33 and 45. -
Microbiome, Infection and Inflammation in Infertility
Chapter 8 Microbiome, Infection and Inflammation in Infertility Reza Peymani and Alan DeCherney Additional information is available at the end of the chapter http://dx.doi.org/10.5772/63090 Abstract The implantation mechanism and process are very complex and require a precise interac‐ tion between the embryo and endometrium. The failure to implant is thought to be due to implantation environment factors or embryonic factors. A suitable condition of the uterine cavity is essential for successful reproduction. Inflam‐ mation can be a part of the normal physiologic process during implantation; however, there are also pathologic sources of inflammation that can adversely affect the uterine cavity and endometrial receptivity. Chronic Endometritis is usually asymptomatic and is defined histologically by the pres‐ ence of plasma cells in an endometrial biopsy. It is mostly associated with the gonorrheal or chlamydial also non-sexually transmitted infections including E-coli, streptococcus, staphylococcus, enterococcus faecalis, mycoplasma, urea plasma and yeast. However, of‐ ten a causal organism can not be identified. Available evidence suggests that chronic subclinical endometritis is relatively common in women with symptomatic lower genital tract infections, including cervicitis and recur‐ rent bacterial vaginosis and may not be altogether rare even in asymptomatic infertile women. Mucopurulent cervicitis is highly associated with chlamydial and mycoplasma infections and both organisms, in turn, are associated with chronic endometritis, which likely plays a role in the pathogenesis of tubal factor infertility. There is also a growing interest in the Microbiome of the reproductive tract. The Vaginal and Uterine Microbiome have been partially characterized and shown to be related to ob‐ stetric outcomes. -
Chapter 28 *Lecture Powepoint
Chapter 28 *Lecture PowePoint The Female Reproductive System *See separate FlexArt PowerPoint slides for all figures and tables preinserted into PowerPoint without notes. Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Introduction • The female reproductive system is more complex than the male system because it serves more purposes – Produces and delivers gametes – Provides nutrition and safe harbor for fetal development – Gives birth – Nourishes infant • Female system is more cyclic, and the hormones are secreted in a more complex sequence than the relatively steady secretion in the male 28-2 Sexual Differentiation • The two sexes indistinguishable for first 8 to 10 weeks of development • Female reproductive tract develops from the paramesonephric ducts – Not because of the positive action of any hormone – Because of the absence of testosterone and müllerian-inhibiting factor (MIF) 28-3 Reproductive Anatomy • Expected Learning Outcomes – Describe the structure of the ovary – Trace the female reproductive tract and describe the gross anatomy and histology of each organ – Identify the ligaments that support the female reproductive organs – Describe the blood supply to the female reproductive tract – Identify the external genitalia of the female – Describe the structure of the nonlactating breast 28-4 Sexual Differentiation • Without testosterone: – Causes mesonephric ducts to degenerate – Genital tubercle becomes the glans clitoris – Urogenital folds become the labia minora – Labioscrotal folds -
Chapter 24 Primary Sex Organs = Gonads Produce Gametes Secrete Hormones That Control Reproduction Secondary Sex Organs = Accessory Structures
Anatomy Lecture Notes Chapter 24 primary sex organs = gonads produce gametes secrete hormones that control reproduction secondary sex organs = accessory structures Development and Differentiation A. gonads develop from mesoderm starting at week 5 gonadal ridges medial to kidneys germ cells migrate to gonadal ridges from yolk sac at week 7, if an XY embryo secretes SRY protein, the gonadal ridges begin developing into testes with seminiferous tubules the testes secrete androgens, which cause the mesonephric ducts to develop the testes secrete a hormone that causes the paramesonephric ducts to regress by week 8, in any fetus (XX or XY), if SRY protein has not been produced, the gondal ridges begin to develop into ovaries with ovarian follicles the lack of androgens causes the paramesonephric ducts to develop and the mesonephric ducts to regress B. accessory organs develop from embryonic duct systems mesonephric ducts / Wolffian ducts eventually become male accessory organs: epididymis, ductus deferens, ejaculatory duct paramesonephric ducts / Mullerian ducts eventually become female accessory organs: oviducts, uterus, superior vagina C. external genitalia are indeterminate until week 8 male female genital tubercle penis (glans, corpora cavernosa, clitoris (glans, corpora corpus spongiosum) cavernosa), vestibular bulb) urethral folds fuse to form penile urethra labia minora labioscrotal swellings fuse to form scrotum labia majora urogenital sinus urinary bladder, urethra, prostate, urinary bladder, urethra, seminal vesicles, bulbourethral inferior vagina, vestibular glands glands Strong/Fall 2008 Anatomy Lecture Notes Chapter 24 Male A. gonads = testes (singular = testis) located in scrotum 1. outer coverings a. tunica vaginalis =double layer of serous membrane that partially surrounds each testis; (figure 24.29) b. -
Echography of the Cervix and Uterus During the Proliferative and Secretory Phases of the Menstrual Cycle in Bonnet Monkeys (Macaca Radiata)
Journal of the American Association for Laboratory Animal Science Vol 53, No 1 Copyright 2014 January 2014 by the American Association for Laboratory Animal Science Pages 18–23 Echography of the Cervix and Uterus during the Proliferative and Secretory Phases of the Menstrual Cycle in Bonnet Monkeys (Macaca radiata) Uddhav K Chaudhari,1,* Siddnath M Metkari,2 Dhyananjay D Manjaramkar,2 Geetanjali Sachdeva,1 Rajendra Katkam,1 Atmaram H Bandivdekar,3 Abhishek Mahajan,4 Meenakshi H Thakur,4 and Sanjiv D Kholkute1 We undertook the present study to investigate the echographic characteristics of the uterus and cervix of female bonnet monkeys (Macaca radiata) during the proliferative and secretory phases of the menstrual cycle. The cervix was tortuous in shape and measured 2.74 ± 0.30 cm (mean ± SD) in width by 3.10 ± 0.32 cm in length. The cervical lumen contained 2 or 3 col- liculi, which projected from the cervical canal. The echogenicity of cervix varied during proliferative and secretory phases. The uterus was pyriform in shape (2.46 ± 0.28 cm × 1.45 ± 0.19 cm) and consisted of serosa, myometrium, and endometrium. The endometrium generated a triple-line pattern; the outer and central lines were hyperechogenic, whereas the inner line was hypoechogenic. The endometrium was significantly thicker during the secretory phase (0.69 ± 0.12 cm) than during the proliferative phase (0.43 ± 0.15 cm). Knowledge of the echogenic changes in the female reproductive organs of bonnet monkeys during a regular menstrual cycle may facilitate understanding of other physiologic and pathophysiologic changes. Ultrasound imaging is a noninvasive, atraumatic, and simple Materials and Methods method to assess various organs in humans and nonhuman pri- Animals and husbandry practices. -
2021 – the Following CPT Codes Are Approved for Billing Through Women’S Way
WHAT’S COVERED – 2021 Women’s Way CPT Code Medicare Part B Rate List Effective January 1, 2021 For questions, call the Women’s Way State Office 800-280-5512 or 701-328-2389 • CPT codes that are specifically not covered are 77061, 77062 and 87623 • Reimbursement for treatment services is not allowed. (See note on page 8). • CPT code 99201 has been removed from What’s Covered List • New CPT codes are in bold font. 2021 – The following CPT codes are approved for billing through Women’s Way. Description of Services CPT $ Rate Office Visits New patient; medically appropriate history/exam; straightforward decision making; 15-29 minutes 99202 72.19 New patient; medically appropriate history/exam; low level decision making; 30-44 minutes 99203 110.77 New patient; medically appropriate history/exam; moderate level decision making; 45-59 minutes 99204 165.36 New patient; medically appropriate history/exam; high level decision making; 60-74 minutes. 99205 218.21 Established patient; evaluation and management, may not require presence of physician; 99211 22.83 presenting problems are minimal Established patient; medically appropriate history/exam, straightforward decision making; 10-19 99212 55.88 minutes Established patient; medically appropriate history/exam, low level decision making; 20-29 minutes 99213 90.48 Established patient; medically appropriate history/exam, moderate level decision making; 30-39 99214 128.42 minutes Established patient; comprehensive history exam, high complex decision making; 40-54 minutes 99215 128.42 Initial comprehensive -
Identification of Progressive Cervical Squamous
Aus dem Institut für Cytopathologie der Heinrich-Heine Universität Düsseldorf Direktor: Universitätsprofessor Dr. med. A. Böcking IDENTIFICATION OF PROGRESSIVE CERVICAL SQUAMOUS INTRAEPITHELIAL LESIONS USING DNA-IMAGE-CYTOMETRY A STUDY ON DIAGNOSTIC VALIDITY AND RELIABILITY Dissertation zur Erlangung des Grades eines Doktors der Medizin Der Medizinischen Fakultät der Heinrich-Heine-Universität Düsseldorf vorgelegt von Vu Quoc Huy NGUYEN 2003 Als Inauguraldissertation gedruckt mit Genehmigung der Medizinischen Fakultät der Heinrich-Heine-Universität Düsseldorf gez.: Univ.-Prof. Dr. med. Dr. phil. Alfons Labisch, M.A. Dekan Referent: Univ.-Prof. Dr. med. A. Böcking Korreferent: Priv.-Doz. Dr. med. V. Küppers My wife, Phương Anh My children, Phương Thảo and Quốc Bảo TABLE OF CONTENTS 4 TABLE OF CONTENTS 1. INTRODUCTION .........................................................................................................6 1.1. Epidemiology of cervical cancer and its precursors .....................................6 1.1.1. Incidence of cervical cancer and its precursors....................................6 1.1.2. Causal factors of cervical cancer and precursors.................................7 1.1.3. Natural history of cervical intraepithelial lesions ..................................8 1.2. Diagnostic validity of methods used in the fight against cervical cancer and its precursors.............................................................................................10 1.2.1. Diagnostic validity of cytology and histology .....................................10 -
Comparative Accuracy of Anal and Cervical Cytology in Screening for Moderate to Severe Dysplasia by Magnification Guided Punch Biopsy: a Meta-Analysis
Comparative Accuracy of Anal and Cervical Cytology in Screening for Moderate to Severe Dysplasia by Magnification Guided Punch Biopsy: A Meta-Analysis Wm. Christopher Mathews*, Wollelaw Agmas, Edward Cachay Department of Medicine, University of California San Diego, San Diego, California, United States of America Abstract Background: The accuracy of screening for anal cancer precursors relative to screening for cervical cancer precursors has not been systematically examined. The aim of the current meta-analysis was to compare the relative accuracy of anal cytology to cervical cytology in discriminating between histopathologic high grade and lesser grades of dysplasia when the reference standard biopsy is obtained using colposcope magnification. Methods and Findings: The outcome metric of discrimination was the receiver operating characteristic (ROC) curve area. Random effects meta-analysis of eligible studies was performed with examination of sources of heterogeneity that included QUADAS criteria and selected covariates, in meta-regression models. Thirty three cervical and eleven anal screening studies were found to be eligible. The primary meta-analytic comparison suggested that anal cytologic screening is somewhat less discriminating than cervical cytologic screening (ROC area [95% confidence interval (C.I.)]: 0.834 [0.809–0.859] vs. 0.700 [0.664–0.735] for cervical and anal screening, respectively). This finding was robust when examined in meta-regression models of covariates differentially distributed by screening setting (anal, cervical). Conclusions: Anal cytologic screening is somewhat less discriminating than cervical cytologic screening. Heterogeneity of estimates within each screening setting suggests that other factors influence estimates of screening accuracy. Among these are sampling and interpretation errors involving both cytology and biopsy as well as operator skill and experience. -
Cervicography: an Intermediate Triage Test for the Evaluation O F Cervical Atypia Daron G
Cervicography: An Intermediate Triage Test for the Evaluation o f Cervical Atypia Daron G. Ferris, MD; Peter Payne, MD; Lawrence E. Frisch, MD Augusta and Athens, Georgia, and Areata, California Background. A substantial number of abnormal Papani pia. The histologic specimens confirmed evidence of colaou (Pap) smears are reported as demonstrating “cy cervical dysplasia for 166 women. Of these women, tologic atypia.” This finding may actually represent pre- cervicography detected 74.7% of those who had mild malignant cervical disease. Some of these patients may dysplasia, 87.5% of those who had moderate dysplasia, not be able to afford definitive colposcopic examina 75% of those who had severe dysplasia, and the one tions, and simply repeating cytologic testing may result patient who had cervical cancer. Most (93%) of the in missed treatable disease. The purpose of this study women with dysplasia that was undetected by cervicog was to evaluate the use of cervicography as an interme raphy had mild dysplasia. diate triage test for women with atypical cervical cytol ogy- Conclusions. Cervicography may be an effective inter Methods. Women with a recent smear demonstrating mediate triage test for the evaluation of young women otologic atypia were evaluated using colposcopy, bi with Pap smears demonstrating cytologic atypia. opsy, and cervicography. Key words. Cervix dysplasia; cervix neoplasms; cytolog- Results. Colposcopically directed cervical biopsies were ical techniques; cytology; cervicitis; photography. obtained from 224 of 685 women with cytologic aty ( / Fam Proa 1993; 37:463-468) Of the abnormal Papanicolaou (Pap) smears collected cytology smear.3 Benign cellular changes of infection, from young women, 56% are reported as demonstrating inflammation, repair, and atypia, once known collectively cytologic atypia, or, more specifically, atypical squamous as a class II Pap smear, are now reported as separate cells of undetermined significance (ASCUS).1 The reason entities.