Is There Any Reason of Irritating Vulvar Itching?
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Vaginal and Vulvar Cancer 10.1136/Ijgc-2020-ESGO.178
Int J Gynecol Cancer: first published as 10.1136/ijgc-2020-ESGO.177 on 4 December 2020. Downloaded from Abstracts 520 LONG TERM FOLLOW UP AFTER DIAGNOSIS OF Introduction/Background Since the introduction of the S2K GESTATIONAL TROPHOBLASTIC DISEASE AWMF guideline-based sentinel node biopsy technique in uni- focal vulvar cancer (diameter of <4 cm) and unsuspicious Pedro Corvelo Freitas, Beatriz Mira, António Guimarães, Ana Opinião, Hugo Nunes, Ana Francisca Jorge, Fátima Vaz, António Moreira. Instituto Português de Oncologia de Lisboa groin lymph nodes, the morbidity rate of patients has signifi- Francisco Gentil cantly decreased in Germany. The groin recurrence rate after IFL is vary from 0% to 5.8%, in contrast to 2.3% (95% CI, 10.1136/ijgc-2020-ESGO.176 0.6% to 5%) in unifocal vulvar cancer vs 3% (95% CI, 1% to 6%) in multifocal vulvar cancer after SLNB only, as sug- Introduction/Background The spectrum of Gestational tropho- gested in the GRoningen INternational Study on Sentinel blastic disease (GTD) ranges from pre-malignant conditions of node in Vulvar cancer (GROINSS-V-I) in 2008. Current guide- complete (CHM) and partial (PHM) hydatidiform moles to the lines suggest that in cases of metastasis of unilateral sentinel malignant invasive mole, choriocarcinoma (CC) and very rare lymph node (SLN) biopsy (B), groin node dissection, namely placental site trophoblastic tumour/epithelioid trophoblastic inguinofemoral lymphadenectomy (IFL), should be performed tumour (PSTT/ETT). Gestational trophoblastic neoplasia (GTN) bilaterally. However, a publication by Woelber et al. in Ger- are highly responsive to chemotherapy (CT) and with appropri- many and and Nica et al. -
Pembrolizumab in Vaginal and Vulvar Squamous Cell Carcinoma: a Case Series from a Phase II Basket Trial Jefrey A
www.nature.com/scientificreports OPEN Pembrolizumab in vaginal and vulvar squamous cell carcinoma: a case series from a phase II basket trial Jefrey A. How 1, Amir A. Jazaeri 1, Pamela T. Soliman1, Nicole D. Fleming1, Jing Gong2, Sarina A. Piha‑Paul2, Filip Janku 2, Bettzy Stephen 2 & Aung Naing 2* Vaginal and vulvar squamous cell carcinoma (SCC) are rare tumors that can be challenging to treat in the recurrent or metastatic setting. We present a case series of patients with vaginal or vulvar SCC who were treated with single‑agent pembrolizumab as part of a phase II basket clinical trial to evaluate efcacy and safety. Two cases of recurrent and metastatic vaginal SCC, with multiple prior lines of systemic chemotherapy and radiation, received pembrolizumab. One patient had signifcant reduction (81%) in target tumor lesions prior to treatment discontinuation at cycle 10 following confrmed progression of disease with new metastatic lesions (stable disease by irRECIST criteria). In contrast, the other patient with vaginal SCC discontinued treatment after cycle 3 due to disease progression. Both patients had PD‑L1 positive vaginal tumors and tolerated treatment well. One case of recurrent vulvar SCC with multiple surgical resections and prior progression on systemic carboplatin had a 30% reduction in her target tumor lesions following pembrolizumab treatment with a PD‑L1 positive tumor. Treatment was discontinued for grade 3 mucositis after cycle 5. Pembrolizumab may provide some clinical beneft to some patients with vaginal or vulvar SCC and is overall safe to utilize in this population. Future studies are needed to evaluate the efcacy of pembrolizumab in these rare tumor types and to identify predictive biomarkers of response. -
The Vulva Vaginal Diseases in Daily Practice Layout 1
Experimental & Clinical Article Gynecology; and Gynecologial Onncology The Vulva / Vaginal Diseases in Daily Practice Gamze S. ÇAĞLAR1, Elif D. ÖZDEMİR1, Sevim D. CENGİZ1, Handan DOĞAN2 Ankara, Turkey OBJECTIVE: To emphasize the neglected vulva/vaginal lesions and symptoms commonly encountered in daily practice. STUDY DESIGN: The data of 98 patients with vulva or vaginal biopsies were collected retrospectively. The histopathological diagnosis of 82(83.67%) vulvar and 16(16.32%) vaginal biopsy cases were eval- uated. RESULTS: The most common symptom was mass in 67% and 62% of cases in vulvar and vaginal re- gion, respectively. Among the vulvar lesions the most frequent histopathological diagnoses were condy- loma acuminatum (20.73%), hyperkeratotic papilloma (14.63%), non-spesific inflammatory changes (12.19%), fibroepithelial polyp (9.75%) and bartholin cyst (8.53%). On the other hand, the histopatolog- ical evaluation of the vaginal lesions revealed vaginal stromal polyp (25%) and gartner cyst (25%) as the most frequent lesions. CONCLUSIONS: The results of the study document lesions commonly not well known or disregarded by gynecologists. The literature is inconclusive about vulvavaginal diseases. Expanded data will help the clinicians in making correct diagnoses and patient managament. Key Words: Fibroepithelial polyp, Hyperkeratotic papilloma, Stromal polyp, Vaginal diseases, Vulvar diseases. Gynecol Obstet Reprod Med 2011;17:155-159 Introduction The clinicians should be aware of these physiological changes that will help in guiding the vulvar/vaginal symptoms Vulva is once called forgetten pelvic organ and related and disorders in daily clinical practice. There is limited data symptoms are usually considered as unimportant.1 The most about the most common reported histopathological diagnoses common compliants in women admitting to gynecology clin- and management in vulvavaginal diseases. -
Incidence and Cost of Anal, Penile, Vaginal and Vulvar Cancer in Denmark Jens Olsen1*, Tine Rikke Jørgensen2, Kristian Kofoed3 and Helle Kiellberg Larsen3
Olsen et al. BMC Public Health 2012, 12:1082 http://www.biomedcentral.com/1471-2458/12/1082 RESEARCH ARTICLE Open Access Incidence and cost of anal, penile, vaginal and vulvar cancer in Denmark Jens Olsen1*, Tine Rikke Jørgensen2, Kristian Kofoed3 and Helle Kiellberg Larsen3 Abstract Background: Besides being a causative agent for genital warts and cervical cancer, human papillomavirus (HPV) contributes to 40-85% of cases of anal, penile, vaginal and vulvar cancer and precancerous lesions. HPV types 16 & 18 in particular contribute to 74-93% of these cases. Overall the number of new cases of these four cancers may be relatively high implying notable health care cost to society. The aim of this study was to estimate the incidence and the health care sector costs of anal, penile, vaginal and vulvar cancer. Methods: New anogenital cancer patients were identified from the Danish National Cancer Register using ICD-10 diagnosis codes. Resource use in the health care sector was estimated for the year prior to diagnosis, and for the first, second and third years after diagnosis. Hospital resource use was defined in terms of registered hospital contacts, using DRG (Diagnosis Related Groups) and DAGS (Danish Outpatient Groups System) charges as cost estimates for inpatient and outpatient contacts, respectively. Health care consumption by cancer patients diagnosed in 2004–2007 was compared with that by an age- and sex-matched cohort without cancer. Hospital costs attributable to four anogenital cancers were estimated using regression analysis. Results: The annual incidence of anal cancer in Denmark is 1.9 per 100,000 persons. The corresponding incidence rates for penile, vaginal and vulvar cancer are 1.7, 0.9 and 3.6 per 100,000 males/females, respectively. -
Prioritization of Health Services
PRIORITIZATION OF HEALTH SERVICES A Report to the Governor and the 74th Oregon Legislative Assembly Oregon Health Services Commission Office for Oregon Health Policy and Research Department of Administrative Services 2007 TABLE OF CONTENTS List of Figures . iii Health Services Commission and Staff . .v Acknowledgments . .vii Executive Summary . ix CHAPTER ONE: A HISTORY OF HEALTH SERVICES PRIORITIZATION UNDER THE OREGON HEALTH PLAN Enabling Legislatiion . 3 Early Prioritization Efforts . 3 Gaining Waiver Approval . 5 Impact . 6 CHAPTER TWO: PRIORITIZATION OF HEALTH SERVICES FOR 2008-09 Charge to the Health Services Commission . .. 25 Biennial Review of the Prioritized List . 26 A New Prioritization Methodology . 26 Public Input . 36 Next Steps . 36 Interim Modifications to the Prioritized List . 37 Technical Changes . 38 Advancements in Medical Technology . .42 CHAPTER THREE: CLARIFICATIONS TO THE PRIORITIZED LIST OF HEALTH SERVICES Practice Guidelines . 47 Age-Related Macular Degeneration (AMD) . 47 Chronic Anal Fissure . 48 Comfort Care . 48 Complicated Hernias . 49 Diagnostic Services Not Appearing on the Prioritized List . 49 Non-Prenatal Genetic Testing . 49 Tuberculosis Blood Test . 51 Early Childhood Mental Health . 52 Adjustment Reactions In Early Childhood . 52 Attention Deficit and Hyperactivity Disorders in Early Childhood . 53 Disruptive Behavior Disorders In Early Childhood . 54 Mental Health Problems In Early Childhood Related To Neglect Or Abuse . 54 Mood Disorders in Early Childhood . 55 Erythropoietin . 55 Mastocytosis . 56 Obesity . 56 Bariatric Surgery . 56 Non-Surgical Management of Obesity . 58 PET Scans . 58 Prenatal Screening for Down Syndrome . 59 Prophylactic Breast Removal . 59 Psoriasis . 59 Reabilitative Therapies . 60 i TABLE OF CONTENTS (Cont’d) CHAPTER THREE: CLARIFICATIONS TO THE PRIORITIZED LIST OF HEALTH SERVICES (CONT’D) Practice Guidelines (Cont’d) Sinus Surgery . -
Pruritus Vulvae
628 BRITISH MEDICAL JOURNAL 17 MARCH 1973 may wronglly lead to the diagnosis of primary hyperaldo- 13 Mitchell, J. D., Baxter, T. J., Blair-West, J. R., and McCredie, D. A., Archives of Disease in Childhood, 1970, 45, 376. steronism and even to the excision of the wrong endocrine 14 Voute, P. A., Meer, J. van der, and Staugaard-Kloosterziel, W., Acta Endocrinologica, 1971, 67, 197. Br Med J: first published as 10.1136/bmj.1.5854.628 on 17 March 1973. Downloaded from gland. 15 Hudson, J. B., Chobanian, A. V., and Relman, A. S., New England The opposite clinical syndrome-primary lack of renin or J'ournal of Medicine, 1957, 257, 529. 16 Jacobs, D. R., and Posner, J. B., Metabolism, 1964, 13, 522. hyporeninism-has also been recognized recently. In this 17 Vagnucci, A. H., Journal of Clinical Endocrinology and Metabolism, 1969, disease primary lack of renin (and hence of its active pro- 29, 279. 18 Perez, G., Siegel, L., and Schreiner, G. E., Annals of Internal Medicine, duct angiotension II) apparently leads to selective deficiency 1972, 76, 757. of aldosterone associated with normal cortisol production. 19 Ferrara, E., Werk, E., Hanenson, I., Privirera, P., and Kenyon, C., Clinical Research, 1970, 18, 602. The literature contains reference to some 20 cases of isolated 20 Schambelan, M., Stockigt, J. R., and Biglieri, E. G., New England J ournal of Medicine, 1972, 287, 573. analdosteronism, the first a report by J. B. Hudson and his 21 Weidman, P., et Clinical Research, 1972, 20, 249. colleagues15 in 1957. Only recently however has the primary al., deficiency been recognized as renin lack in at least some of these patients. -
Vaginal Cancer, Risk Factors, and Prevention Risk Factors for Vaginal
cancer.org | 1.800.227.2345 Vaginal Cancer, Risk Factors, and Prevention Risk Factors A risk factor is anything that affects your chance of getting a disease such as cancer. Learn more about the risk factors for vaginal cancer. ● Risk Factors for Vaginal Cancer ● What Causes Vaginal Cancer? Prevention There's no way to completely prevent cancer. But there are things you can do that might help lower your risk. Learn more here. ● Can Vaginal Cancer Be Prevented? Risk Factors for Vaginal Cancer A risk factor is anything that affects your chance of getting a disease such as cancer. Different cancers have different risk factors. Some risk factors, like smoking, can be changed. Others, like a person’s age or family history, can’t be changed. But having a risk factor, or even many, does not mean that you will get the disease. And 1 ____________________________________________________________________________________American Cancer Society cancer.org | 1.800.227.2345 some people who get the disease may not have any known risk factors. Scientists have found that certain risk factors make a woman more likely to develop vaginal cancer. But many women with vaginal cancer don’t have any clear risk factors. And even if a woman with vaginal cancer has one or more risk factors, it’s impossible to know for sure how much that risk factor contributed to causing the cancer. Age Squamous cell cancer of the vagina occurs mainly in older women. It can happen at any age, but few cases are found in women younger than 40. Almost half of cases occur in women who are 70 years old or older. -
Vulvar Cancer Early Detection, Diagnosis, and Staging Detection and Diagnosis
cancer.org | 1.800.227.2345 Vulvar Cancer Early Detection, Diagnosis, and Staging Detection and Diagnosis Finding cancer early -- when it's small and before it has spread -- often allows for more treatment options. Some early cancers may have signs and symptoms that can be noticed, but that's not always the case. ● Can Vulvar Cancer Be Found Early? ● Signs and Symptoms of Vulvar Cancers and Pre-Cancers ● Tests for Vulvar Cancer Stages and Outlook (Prognosis) After a cancer diagnosis, staging provides important information about the extent of cancer in the body and anticipated response to treatment. ● Vulvar Cancer Stages ● Survival Rates for Vulvar Cancer Questions to Ask About Vulvar Cancer Here are some questions you can ask your cancer care team to help you better understand your cancer diagnosis and treatment options. ● Questions to Ask Your Doctor About Vulvar Cancer 1 ____________________________________________________________________________________American Cancer Society cancer.org | 1.800.227.2345 Can Vulvar Cancer Be Found Early? Having pelvic exams and knowing any signs and symptoms of vulvar cancer greatly improve the chances of early detection and successful treatment. If you have any of the problems discussed in Signs and Symptoms of Vulvar Cancers and Pre-Cancers, you should see a doctor. If the doctor finds anything abnormal during a pelvic examination, you may need more tests to figure out what is wrong. This may mean referral to a gynecologist (specialist in problems of the female genital system). Knowing what to look for can sometimes help with early detection, but it is even better not to wait until you notice symptoms. -
NCCN Guidelines for Penile Cancer from Version 1.2019 Include
NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Penile Cancer Version 2.2019 — May 13, 2019 NCCN.org Continue Version 2.2019, 05/13/19 © 2019 National Comprehensive Cancer Network® (NCCN®), All rights reserved. The NCCN Guidelines® and this illustration may not be reproduced in any form without the express written permission of NCCN. NCCN Guidelines Index NCCN Guidelines Version 2.2019 Table of Contents Penile Cancer Discussion *Thomas W. Flaig, MD †/Chair Harry W. Herr, MD ϖ Sumanta K. Pal, MD † University of Colorado Cancer Center Memorial Sloan Kettering Cancer Center City of Hope National Medical Center *Philippe E. Spiess, MD, MS ϖ/Vice Chair Christopher Hoimes, MD † Anthony Patterson, MD ϖ Moffitt Cancer Center Case Comprehensive Cancer Center/ St. Jude Children’s Research Hospital/ University Hospitals Seidman Cancer Center The University of Tennessee Neeraj Agarwal, MD ‡ † and Cleveland Clinic Taussig Cancer Institute Health Science Center Huntsman Cancer Institute at the University of Utah Brant A. Inman, MD, MSc ϖ Elizabeth R. Plimack, MD, MS † Duke Cancer Institute Fox Chase Cancer Center Rick Bangs, MBA Patient Advocate Masahito Jimbo, MD, PhD, MPH Þ Kamal S. Pohar, MD ϖ University of Michigan Rogel Cancer Center The Ohio State University Comprehensive Stephen A. Boorjian, MD ϖ Cancer Center - James Cancer Hospital Mayo Clinic Cancer Center A. Karim Kader, MD, PhD ϖ and Solove Research Institute UC San Diego Moores Cancer Center Mark K. Buyyounouski, MD, MS § Michael P. Porter, MD, MS ϖ Stanford Cancer Institute Subodh M. Lele, MD ≠ Fred Hutchinson Cancer Research Center/ Fred & Pamela Buffett Cancer Center Sam Chang, MD ¶ Seattle Cancer Care Alliance Vanderbilt-Ingram Cancer Center Joshua J. -
Prognostic Significance of HPV and P16 Status in Men Diagnosed with Penile Cancer: a Systematic Review and Meta-Analysis
Published OnlineFirst July 9, 2018; DOI: 10.1158/1055-9965.EPI-18-0322 Review Cancer Epidemiology, Biomarkers Prognostic Significance of HPV and p16 Status in & Prevention Men Diagnosed with Penile Cancer: A Systematic Review and Meta-analysis Freja Lærke Sand1, Christina Louise Rasmussen1, Marie Hoffmann Frederiksen2, Klaus Kaae Andersen2, and Susanne K. Kjaer1,3 Abstract It has been shown that human papillomavirus (HPV) of DSS, we included 649 men with penile cancer tested for and p16 status has prognostic value in some HPV-associ- HPV (27% were HPV-positive) and 404 men tested for p16 ated cancers. However, studies examining survival in men expression (47% were p16-positive). The pooled HRHPV of with penile cancer according to HPV or p16 status are often DSS was 0.61 [95% confidence interval (CI), 0.38–0.98], inconclusive, mainly because of small study populations. andthepooledHRp16 of DSS was 0.45 (95% CI, 0.30– The aim of this systematic review and meta-analysis was to 0.69). In conclusion, men with HPV or p16-positive penile examine the association between HPV DNA and p16 status cancer have a significantly more favorable DSS compared and survival in men diagnosed with penile cancer. Multi- with men with HPV or p16-negative penile cancer. These ple electronic databases were searched. Twenty studies findings point to the possible clinical value of HPV and were ultimately included and study-specific and pooled p16 testing when planning the most optimal management HRs of overall survival and disease-specific survival (DSS) and follow-up strategy. Cancer Epidemiol Biomarkers Prev; 27(10); 1– were calculated using a fixed effects model. -
The Older Woman with Vulvar Itching and Burning Disclosures Old Adage
Disclosures The Older Woman with Vulvar Mark Spitzer, MD Itching and Burning Merck: Advisory Board, Speakers Bureau Mark Spitzer, MD QiagenQiagen:: Speakers Bureau Medical Director SABK: Stock ownership Center for Colposcopy Elsevier: Book Editor Lake Success, NY Old Adage Does this story sound familiar? A 62 year old woman complaining of vulvovaginal itching and without a discharge self treatstreats with OTC miconazole.miconazole. If the only tool in your tool Two weeks later the itching has improved slightly but now chest is a hammer, pretty she is burning. She sees her doctor who records in the chart that she is soon everyyggthing begins to complaining of itching/burning and tells her that she has a look like a nail. yeast infection and gives her teraconazole cream. The cream is cooling while she is using it but the burning persists If the only diagnoses you are aware of She calls her doctor but speaks only to the receptionist. She that cause vulvar symptoms are Candida, tells the receptionist that her yeast infection is not better yet. The doctor (who is busy), never gets on the phone but Trichomonas, BV and atrophy those are instructs the receptionist to call in another prescription for teraconazole but also for thrthreeee doses of oral fluconazole the only diagnoses you will make. and to tell the patient that it is a tough infection. A month later the patient is still not feeling well. She is using cold compresses on her vulva to help her sleep at night. She makes an appointment. The doctor tests for BV. -
Diagnosing and Managing Vulvar Disease
Diagnosing and Managing Vulvar Disease John J. Willems, M.D. FRCSC, FACOG Chairman, Department of Obstetrics & Gynecology Scripps Clinic La Jolla, California Objectives: IdentifyIdentify thethe majormajor formsforms ofof vulvarvulvar pathologypathology DescribeDescribe thethe appropriateappropriate setupsetup forfor vulvarvulvar biopsybiopsy DescribeDescribe thethe mostmost appropriateappropriate managementmanagement forfor commonlycommonly seenseen vulvarvulvar conditionsconditions Faculty Disclosure Unlabeled Product Company Nature of Affiliation Usage Warner Chilcott Speakers Bureau None ClassificationClassification ofof VulvarVulvar DiseaseDisease byby ClinicalClinical CharacteristicCharacteristic • Red lesions • White lesions • Dark lesions •Ulcers • Small tumors • Large tumors RedRed LesionsLesions • Candida •Tinea • Reactive vulvitis • Seborrheic dermatitis • Psoriasis • Vulvar vestibulitis • Paget’s disease Candidal vulvitis Superficial grayish-white film is often present Thick film of candida gives pseudo-ulcerative appearance. Acute vulvitis from coital trauma Contact irritation from synthetic fabrics Nomenclature SubtypesSubtypes ofof VulvodyniaVulvodynia:: VulvarVulvar VestibulitisVestibulitis SyndromeSyndrome (VVS)(VVS) alsoalso knownknown asas:: • Vestibulodynia • localized vulvar dysesthesia DysestheticDysesthetic VulvodyniaVulvodynia alsoalso knownknown asas:: • “essential” vulvodynia • generalized vulvar dysesthesia Dysesthesia Unpleasant,Unpleasant, abnormalabnormal sensationsensation examplesexamples include:include: