Vaginal cancer is a rare malignancy representing 1-2% of gynecologic cancers. Most cases are metastatic from cervical or endometrial cancer. Risk factors include HPV infection and prior pelvic radiation. Symptoms include abnormal bleeding and discharge. Diagnosis involves biopsy of any suspicious lesions. Treatment typically involves radiation therapy, with surgery reserved for early stage or recurrent disease. Prognosis depends on stage, with 5-year survival rates of 70-80% for stage I but dropping to 0% for stage IV disease. Recurrence rates after radiation range from 10-45% depending on stage.
Vaginal cancer is a rare type of cancer most common in women 60 and older.
Women are more likely to develop vaginal cancer if they have the human papillomavirus (HPV) or if your birth mother took diethylstilbestol (DES) when she was pregnant.
There are several types of vaginal cancer:
Squamous cell carcinoma
About 70 of every 100 cases of vaginal cancer are squamous cell carcinomas. These cancers begin in the squamous cells that make up the epithelial lining of the vagina. These cancers are more common in the upper area of the vagina near the cervix. Squamous cell cancers of the vagina often develop slowly. First, some of the normal cells of the vagina get pre-cancerous changes. Then some of the pre-cancer cells turn into cancer cells. This process can take many years.
The medical term most often used for this pre-cancerous condition is vaginal intraepithelial neoplasia (VAIN). "Intraepithelial" means that the abnormal cells are only found in the surface layer of the vaginal skin (epithelium). There are 3 types of VAIN: VAIN1, VAIN2, and VAIN3, with 3 indicating furthest progression toward a true cancer. VAIN is more common in women who have had their uterus removed (hysterectomy) and in those who were previously treated for cervical cancer or pre-cancer.
In the past, the term dysplasia was used instead of VAIN. This term is used much less now. When talking about dysplasia, there is also a range of increasing progress toward cancer - first, mild dysplasia; next, moderate dysplasia; and then severe dysplasia.
Adenocarcinoma
Cancer that begins in gland cells is called adenocarcinoma. About 15 of every 100 cases of vaginal cancer are adenocarcinomas. The usual type of vaginal adenocarcinoma typically develops in women older than 50. One certain type, called clear cell adenocarcinoma, occurs more often in young women who were exposed to diethylstilbestrol (DES) in utero (when they were in their mother’s womb). (See the section called "What are the risk factors for vaginal cancer?" for more information on DES and clear cell carcinoma.)
Melanoma
Melanomas develop from pigment-producing cells that give skin its color. These cancers usually are found on sun-exposed areas of the skin but can form on the vagina or other internal organs. About 9 of every 100 cases of vaginal cancer are melanomas. Melanoma tends to affect the lower or outer portion of the vagina. The tumors vary greatly in size, color, and growth pattern. More information about melanoma can be found in our document called Melanoma Skin Cancer.
Sarcoma
A sarcoma is a cancer that begins in the cells of bones, muscles, or connective tissue. Up to 4 of every 100 cases of vaginal cancer are sarcomas. These cancers form deep in the wall of the vagina, not on its surface. There are several types of vaginal sarcomas. Rhabdomyosarcoma is the most common type of vaginal sarcoma. It is most often found in children and is rare in adults. A sarcoma called leiomyosarcoma is seen more often in adults.
Vaginal cancer is a rare type of cancer most common in women 60 and older.
Women are more likely to develop vaginal cancer if they have the human papillomavirus (HPV) or if your birth mother took diethylstilbestol (DES) when she was pregnant.
There are several types of vaginal cancer:
Squamous cell carcinoma
About 70 of every 100 cases of vaginal cancer are squamous cell carcinomas. These cancers begin in the squamous cells that make up the epithelial lining of the vagina. These cancers are more common in the upper area of the vagina near the cervix. Squamous cell cancers of the vagina often develop slowly. First, some of the normal cells of the vagina get pre-cancerous changes. Then some of the pre-cancer cells turn into cancer cells. This process can take many years.
The medical term most often used for this pre-cancerous condition is vaginal intraepithelial neoplasia (VAIN). "Intraepithelial" means that the abnormal cells are only found in the surface layer of the vaginal skin (epithelium). There are 3 types of VAIN: VAIN1, VAIN2, and VAIN3, with 3 indicating furthest progression toward a true cancer. VAIN is more common in women who have had their uterus removed (hysterectomy) and in those who were previously treated for cervical cancer or pre-cancer.
In the past, the term dysplasia was used instead of VAIN. This term is used much less now. When talking about dysplasia, there is also a range of increasing progress toward cancer - first, mild dysplasia; next, moderate dysplasia; and then severe dysplasia.
Adenocarcinoma
Cancer that begins in gland cells is called adenocarcinoma. About 15 of every 100 cases of vaginal cancer are adenocarcinomas. The usual type of vaginal adenocarcinoma typically develops in women older than 50. One certain type, called clear cell adenocarcinoma, occurs more often in young women who were exposed to diethylstilbestrol (DES) in utero (when they were in their mother’s womb). (See the section called "What are the risk factors for vaginal cancer?" for more information on DES and clear cell carcinoma.)
Melanoma
Melanomas develop from pigment-producing cells that give skin its color. These cancers usually are found on sun-exposed areas of the skin but can form on the vagina or other internal organs. About 9 of every 100 cases of vaginal cancer are melanomas. Melanoma tends to affect the lower or outer portion of the vagina. The tumors vary greatly in size, color, and growth pattern. More information about melanoma can be found in our document called Melanoma Skin Cancer.
Sarcoma
A sarcoma is a cancer that begins in the cells of bones, muscles, or connective tissue. Up to 4 of every 100 cases of vaginal cancer are sarcomas. These cancers form deep in the wall of the vagina, not on its surface. There are several types of vaginal sarcomas. Rhabdomyosarcoma is the most common type of vaginal sarcoma. It is most often found in children and is rare in adults. A sarcoma called leiomyosarcoma is seen more often in adults.
endometrial cancer
endometrial carcinoma
gynaecological oncology
uterine cancer
uterus
post menopausal bleeding
endometrial neoplasms
gynaecology
cancer
Presentation at Chittaranjan Seva Sadan, Kolkata where Dr Dasgupta was invited as faculty in the CME organized by Medical Education and research Committee, Bengal Obstetrics and Gynaecological Society
this lecture for undergraduates, GP & gynecologists
it includes full simple explanation of CIN (cervical intraepithelial neoplasia)
how to do screening for cervical cancer
methods of screening that include pap smear and HPV testing
it also includes the diagnostic method for the cervical cancer by taking biopsy directed by colposcopy
colposcopy and its rule
how to deal with CIN different grades
follow up after CIN treatment
endometrial cancer
endometrial carcinoma
gynaecological oncology
uterine cancer
uterus
post menopausal bleeding
endometrial neoplasms
gynaecology
cancer
Presentation at Chittaranjan Seva Sadan, Kolkata where Dr Dasgupta was invited as faculty in the CME organized by Medical Education and research Committee, Bengal Obstetrics and Gynaecological Society
this lecture for undergraduates, GP & gynecologists
it includes full simple explanation of CIN (cervical intraepithelial neoplasia)
how to do screening for cervical cancer
methods of screening that include pap smear and HPV testing
it also includes the diagnostic method for the cervical cancer by taking biopsy directed by colposcopy
colposcopy and its rule
how to deal with CIN different grades
follow up after CIN treatment
Ca ovary staging(AJCC 8th Edition& FIGO 2014) and classificationDr.Bhavin Vadodariya
Pathological classification of ovary in details.
Principles of Staging in Ca Ovary.
Staging according to AJCC 8th edition & Figo 2014.
Summary of changes in 8th Edition AJCC
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
263778731218 Abortion Clinic /Pills In Harare ,sisternakatoto
263778731218 Abortion Clinic /Pills In Harare ,ABORTION WOMEN’S CLINIC +27730423979 IN women clinic we believe that every woman should be able to make choices in her pregnancy. Our job is to provide compassionate care, safety,affordable and confidential services. That’s why we have won the trust from all generations of women all over the world. we use non surgical method(Abortion pills) to terminate…Dr.LISA +27730423979women Clinic is committed to providing the highest quality of obstetrical and gynecological care to women of all ages. Our dedicated staff aim to treat each patient and her health concerns with compassion and respect.Our dedicated group ABORTION WOMEN’S CLINIC +27730423979 IN women clinic we believe that every woman should be able to make choices in her pregnancy. Our job is to provide compassionate care, safety,affordable and confidential services. That’s why we have won the trust from all generations of women all over the world. we use non surgical method(Abortion pills) to terminate…Dr.LISA +27730423979women Clinic is committed to providing the highest quality of obstetrical and gynecological care to women of all ages. Our dedicated staff aim to treat each patient and her health concerns with compassion and respect.Our dedicated group of receptionists, nurses, and physicians have worked together as a teamof receptionists, nurses, and physicians have worked together as a team wwww.lisywomensclinic.co.za/
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists
Carcinoma vagina
1. Vaginal CancerVaginal Cancer
Dr Nabeel YahiyaDr Nabeel Yahiya
Junior resident in RadiotherapyJunior resident in Radiotherapy
Kottayam Medical CollegeKottayam Medical College
2. Vaginal CancerVaginal Cancer
Rare tumor representing only 1-2% of all gynecologicRare tumor representing only 1-2% of all gynecologic
malignanciesmalignancies
80-90% are metastatic80-90% are metastatic
cervix or endometrium.cervix or endometrium.
Metastatic cancer from the vulva, ovaries, choriocarcinoma,Metastatic cancer from the vulva, ovaries, choriocarcinoma,
rectosigmoid, and bladder, renal cell carcinoma, rectosigmoid, and bladder, renal cell carcinoma, melanomamelanoma,,
and breast cancer are less commonand breast cancer are less common
Mean age of patients with primary vaginal cancer is 60-65Mean age of patients with primary vaginal cancer is 60-65
yearsyears
3. IntroductionIntroduction
The vagina is a muscular dilatable tubular structureThe vagina is a muscular dilatable tubular structure
averaging 7.5 cm in length that extends from the cervix toaveraging 7.5 cm in length that extends from the cervix to
the vulvathe vulva
10. Vaginal Cancer: PredisposingVaginal Cancer: Predisposing
FactorsFactors
HPV infectionHPV infection
Low socioeconomic statusLow socioeconomic status
History of genital wartsHistory of genital warts
Vaginal discharge or irritationVaginal discharge or irritation
Previously abnormal Pap smearPreviously abnormal Pap smear
Early hysterectomyEarly hysterectomy
Previous pelvic radiation (?)Previous pelvic radiation (?)
In-utero exposure to DESIn-utero exposure to DES
11. Vaginal Cancer precursorsVaginal Cancer precursors
Hallmark of VAINHallmark of VAIN
– cytologic atypia-Pleomorphisim, irreg nuclear contourscytologic atypia-Pleomorphisim, irreg nuclear contours
and chromatin clumpingand chromatin clumping
– Abnormal maturationAbnormal maturation
– nuclear enlargementnuclear enlargement
10-30% progress to Vaginal Ca10-30% progress to Vaginal Ca
12. Vaginal Cancer precursorsVaginal Cancer precursors
VAIN 1-
Proliferation of basal layer
Koilocytotic atypia
Enlarged pleomorphic nuclei
vacuolated cytoplasm
13. Vaginal Cancer precursorsVaginal Cancer precursors
VAIN 2-
Proliferation of basal layer,crowding
and loss of polarity
Koilocytotic atypia
Enlarged pleomorphic nuclei
vacuolated cytoplasm
14. Vaginal Cancer precursorsVaginal Cancer precursors
VAIN 3
Increased proliferation of abnormal basal
and parabasal cells replacing full
thickness of epithelium
15. Vaginal Cancer precursorsVaginal Cancer precursors
VAIN 3VAIN 3
– usually occurs in upper third of vagina and isusually occurs in upper third of vagina and is
multifocal and diffuse in half the cases.multifocal and diffuse in half the cases.
– 1/3 of patients have a hx/o CIN1/3 of patients have a hx/o CIN
– CIN coexists w/ VAIN in 10-20% of ptsCIN coexists w/ VAIN in 10-20% of pts
– Colposcopic findings are similar to those of CINColposcopic findings are similar to those of CIN
(aceto white epithelium with punctations and(aceto white epithelium with punctations and
mosaic patterns)mosaic patterns)
16. Vaginal Cancer precursorsVaginal Cancer precursors
Treatment Options for VAINTreatment Options for VAIN
– Excisional Bx for small lesionsExcisional Bx for small lesions
– Partial VaginectomyPartial Vaginectomy
– Laser VaporizationLaser Vaporization
– Electro coagulationElectro coagulation
– Intravaginal 5FU creamIntravaginal 5FU cream
– RTRT
17. PathologyPathology
Invasive squamous cell carcinoma is found in 75% to 95% ofInvasive squamous cell carcinoma is found in 75% to 95% of
primary vaginal carcinomasprimary vaginal carcinomas
The majority of these lesions tend to be nonkeratinizing andThe majority of these lesions tend to be nonkeratinizing and
moderately differentiated.moderately differentiated.
The well-differentiated lesions may demonstrateThe well-differentiated lesions may demonstrate
keratinization, manifested by squamous pearls andkeratinization, manifested by squamous pearls and
intracellular bridgesintracellular bridges
Grossly, these tumors may manifest as nodular, ulcerated,Grossly, these tumors may manifest as nodular, ulcerated,
indurated, exophytic, or endophytic lesionsindurated, exophytic, or endophytic lesions
19. Histologically, keratinizing, nonkeratinizing, basaloid, warty,Histologically, keratinizing, nonkeratinizing, basaloid, warty,
and verrucous variants have been describedand verrucous variants have been described
20. Vaginal Adenosis and AdenocarcinomaVaginal Adenosis and Adenocarcinoma
Adenocarcinoma is found in 5% to 10% of all vaginalAdenocarcinoma is found in 5% to 10% of all vaginal
cancerscancers
The non–clear cell adenocarcinoma frequently arises in theThe non–clear cell adenocarcinoma frequently arises in the
submucosa.submucosa.
When a biopsy of a vaginal lesion reveals adenocarcinoma,When a biopsy of a vaginal lesion reveals adenocarcinoma,
it is important to look for a primary lesion, such asit is important to look for a primary lesion, such as
endometrial cancer, elsewhereendometrial cancer, elsewhere
21. Vaginal adenosis defines the abnormal presence ofVaginal adenosis defines the abnormal presence of
glandular epithelium in the vagina, which is normally devoidglandular epithelium in the vagina, which is normally devoid
of glandular elementsof glandular elements
The glandular epithelial cells may line glands in theThe glandular epithelial cells may line glands in the
submucosa or cover or replace surface squamous cells andsubmucosa or cover or replace surface squamous cells and
are usually located near the surface epitheliumare usually located near the surface epithelium
adenosis is the most common histological abnormality inadenosis is the most common histological abnormality in
women exposed to DES in utero, it is not strictly confined towomen exposed to DES in utero, it is not strictly confined to
this populationthis population
The classic gross appearance of adenosis is red, velvety,The classic gross appearance of adenosis is red, velvety,
grapelike clusters in the vaginagrapelike clusters in the vagina
22. A large cystic focus of adenosis is seen underneath the stratified squamousA large cystic focus of adenosis is seen underneath the stratified squamous
epithelium of the vaginal surfaceepithelium of the vaginal surface
23. Adenosis is associated with 97% of vaginal clear cell cancerAdenosis is associated with 97% of vaginal clear cell cancer
DES-associated CCA has a predilection for the upper third ofDES-associated CCA has a predilection for the upper third of
the vagina and the ectocervixthe vagina and the ectocervix
The most common histologic pattern is tubulocystic followedThe most common histologic pattern is tubulocystic followed
by a solid pattern.by a solid pattern.
The most common cells noted are the clear cell, hobnail cell,The most common cells noted are the clear cell, hobnail cell,
and endometrioid celland endometrioid cell
24. melanomamelanoma
Malignant melanoma of the vagina represents approximatelyMalignant melanoma of the vagina represents approximately
5% of all vaginal neoplasms and approximately 0.7% of all5% of all vaginal neoplasms and approximately 0.7% of all
melanomasmelanomas
Clinically, these tumors present as pigmented masses,Clinically, these tumors present as pigmented masses,
plaques or ulcerative lesions, most frequently on the distalplaques or ulcerative lesions, most frequently on the distal
one-third of the anterior vaginal wall.one-third of the anterior vaginal wall.
However, they may present in a nonpigmented manner.However, they may present in a nonpigmented manner.
Melanomas may display aggressive biological behavior withMelanomas may display aggressive biological behavior with
early and rapid local and systemic failureearly and rapid local and systemic failure
26. The most common of these isThe most common of these is
the embryonalthe embryonal
rhabdomyosarcoma (sarcomarhabdomyosarcoma (sarcoma
botryoides)botryoides)
a highly malignant tumor thata highly malignant tumor that
occurs in the vagina duringoccurs in the vagina during
infancy and early childhoodinfancy and early childhood
(mean age 3 years).(mean age 3 years).
This sarcoma has theThis sarcoma has the
characteristic grosscharacteristic gross
appearance of grape-likeappearance of grape-like
masses that are exophytic andmasses that are exophytic and
can protrude from the vagina.can protrude from the vagina.
27. Lymphomas and small cell carcinomas may also arise in theLymphomas and small cell carcinomas may also arise in the
vagina.vagina.
Small cell carcinomas behave in an aggressive manner,Small cell carcinomas behave in an aggressive manner,
similar to small cell carcinomas arising in other parts of thesimilar to small cell carcinomas arising in other parts of the
bodybody
28.
29. Natural History and Patterns ofNatural History and Patterns of
SpreadSpread
Lesions usually found in the upper vagina on the posteriorLesions usually found in the upper vagina on the posterior
wallwall
50% of Vag Ca ulcerative50% of Vag Ca ulcerative
30% are exophytic30% are exophytic
20%are annular and constricting20%are annular and constricting
Vaginal primary tumors may spread along mucosa to cervixVaginal primary tumors may spread along mucosa to cervix
or vulvaor vulva
Direct extension to bladder, parametria, paracolpos, rectum,Direct extension to bladder, parametria, paracolpos, rectum,
cardinal ligaments, uterosacral ligamentscardinal ligaments, uterosacral ligaments
30. Natural History and Patterns ofNatural History and Patterns of
SpreadSpread
Any of the nodal groups may be involved regardless of theAny of the nodal groups may be involved regardless of the
location of the tumorlocation of the tumor
Inguinal nodes most often involved if lesion is in the lower 1/3Inguinal nodes most often involved if lesion is in the lower 1/3
of the vaginaof the vagina
Clinically apparent inguinal node mets seen in 5-20% ofClinically apparent inguinal node mets seen in 5-20% of
patientspatients
Incidence of pelvic nodes varies with stage and location ofIncidence of pelvic nodes varies with stage and location of
the tumorthe tumor
31. Clinical PresentationClinical Presentation
Abnormal vaginal bleedingAbnormal vaginal bleeding
– 50-75% of patients with primary tumors50-75% of patients with primary tumors
DischargeDischarge
DysuriaDysuria
PainPain
32. Diagnostic Work-upDiagnostic Work-up
Complete history and physicalComplete history and physical
Speculum examination and palpation of the vaginaSpeculum examination and palpation of the vagina
Bimanual pelvic and rectovaginal examinationBimanual pelvic and rectovaginal examination
Pap smear, colposcopy, directed biopsiesPap smear, colposcopy, directed biopsies
34. Axial T1-weighted magnetic resonance images of a patient with stage IIAxial T1-weighted magnetic resonance images of a patient with stage II
squamous cell cancer of the vagina located in the left vaginal fornix withsquamous cell cancer of the vagina located in the left vaginal fornix with
involvement of the left parametriainvolvement of the left parametria
37. 5 Year Survival5 Year Survival
0
10
20
30
40
50
60
70
80
Stage I Stage I I Stage I I I Stage I V
38. Natural History and Patterns ofNatural History and Patterns of
FailureFailure
Stage IStage I
– 10-20% pelvic recurrence, 10-20% distant10-20% pelvic recurrence, 10-20% distant
Stage IIStage II
– 35% pelvic recurrence, 22% distant35% pelvic recurrence, 22% distant
Stage IIIStage III
– 25-45% pelvic recurrence, 23% distant25-45% pelvic recurrence, 23% distant
Stage IVStage IV
– 58% pelvic recurrence, 30% distant58% pelvic recurrence, 30% distant
39. primary vaginal carcinomas treated with definitive RT, theprimary vaginal carcinomas treated with definitive RT, the
10-year actuarial disease-free survival (DFS)10-year actuarial disease-free survival (DFS)
94% for stage 094% for stage 0
75% for stage I75% for stage I
55% for stage II55% for stage II
32% for stage III32% for stage III
0% for those with stage IV.0% for those with stage IV.
40. ManagementManagement
Radiation therapy is the preferred treatmentRadiation therapy is the preferred treatment
for most carcinomas of the vaginafor most carcinomas of the vagina
Surgical therapySurgical therapy
– Early stage lesionEarly stage lesion
– Irradiation failuresIrradiation failures
– Non-epithelial tumorsNon-epithelial tumors
– Stage I Clear cell adenocarcinomas in youngStage I Clear cell adenocarcinomas in young
womenwomen
41. ManagementManagement
SurgerySurgery
– Wide local excision reserved for carcinoma insitu or smallWide local excision reserved for carcinoma insitu or small
superficially invasive lesions that r well demarcatedsuperficially invasive lesions that r well demarcated
– Stage I tumors of the middle or upper third of vaginaStage I tumors of the middle or upper third of vagina
treated with radical hysterovaginectomy and PLNDtreated with radical hysterovaginectomy and PLND
– Stage I tumors of the lower third of vagina which mayStage I tumors of the lower third of vagina which may
encroach on the vulva treated with radicalencroach on the vulva treated with radical
vulvovaginectomy and bilat. groin node dissectionvulvovaginectomy and bilat. groin node dissection
– Pelvic exenteration possible for more invasive lesionsPelvic exenteration possible for more invasive lesions
42. ManagementManagement
Stage IStage I
– Usually managed with RTUsually managed with RT
– Superficial lesions (<5mm) may be treated with vaginalSuperficial lesions (<5mm) may be treated with vaginal
cylinder covering the entire vaginacylinder covering the entire vagina
– Thicker lesions may be treated with vaginal cylinder +Thicker lesions may be treated with vaginal cylinder +
single plane implantsingle plane implant
– EBRT reserved for aggressive lesions (infiltrating orEBRT reserved for aggressive lesions (infiltrating or
poorly differentiated)poorly differentiated)
43. RT…RT…
Selected patients with superficial tumors brachytherapySelected patients with superficial tumors brachytherapy
alone by vaginal cylinders.alone by vaginal cylinders.
60-70Gy 0.5 cm surface LDR60-70Gy 0.5 cm surface LDR
Additional 20-30Gy to tumor aloneAdditional 20-30Gy to tumor alone
HDR, 21-25Gy in 3-5 fractionsHDR, 21-25Gy in 3-5 fractions
Additional 21-25Gy to tumorAdditional 21-25Gy to tumor
44. RT..RT..
Combination of ICA and IBT in lesions thicker than 5mmCombination of ICA and IBT in lesions thicker than 5mm
Vaginal cylinder delivers 45Gy LDR or 21-25Gy by HDR 0.5Vaginal cylinder delivers 45Gy LDR or 21-25Gy by HDR 0.5
cm vaginal mucosacm vaginal mucosa
Additional therapy with interstitial BT to tumor volumeAdditional therapy with interstitial BT to tumor volume
25-35Gy LDR25-35Gy LDR
45. Stage 1 RT..Stage 1 RT..
Combination of EBRT n BT for more aggressive stage 1 withCombination of EBRT n BT for more aggressive stage 1 with
greater infiltration and poor differentiationgreater infiltration and poor differentiation
Recent trend towards combinationRecent trend towards combination
Possible under estimation of submucosal disease or nodalPossible under estimation of submucosal disease or nodal
statusstatus
46. Stage 2Stage 2
Radiation is the primary optionRadiation is the primary option
EBRT + BTEBRT + BT
EBRT 45-50.4GyEBRT 45-50.4Gy
Boost to tumor volume with BT to total dose of 75-80GyBoost to tumor volume with BT to total dose of 75-80Gy
47. Stage 3 n 4Stage 3 n 4
EBRT + BTEBRT + BT
IMRTIMRT
48. Role of Chemotherapy and RadiationRole of Chemotherapy and Radiation
The control rate in the pelvis for stages III and IV patients isThe control rate in the pelvis for stages III and IV patients is
relatively lowrelatively low
about 70% to 80% of the patients have persistent disease orabout 70% to 80% of the patients have persistent disease or
recurrent disease in the pelvis, in spite of high doses ofrecurrent disease in the pelvis, in spite of high doses of
external beam RT and brachytherapyexternal beam RT and brachytherapy
Failure in distant sites does occur in about 25% to 30% ofFailure in distant sites does occur in about 25% to 30% of
the patients with locally advanced tumorsthe patients with locally advanced tumors
49. Therefore, there is a need for better approaches to theTherefore, there is a need for better approaches to the
management of advanced disease such as the use ofmanagement of advanced disease such as the use of
concomitant chemoradiotherapyconcomitant chemoradiotherapy
Agents such as 5-FU, mitomycin-C, and cisplatin haveAgents such as 5-FU, mitomycin-C, and cisplatin have
shown promise when combined with RTshown promise when combined with RT
Advanced cervical cancer has improvement in locoregionalAdvanced cervical cancer has improvement in locoregional
control, overall survival, and disease-free survival forcontrol, overall survival, and disease-free survival for
patients receiving cisplatin-based chemotherapypatients receiving cisplatin-based chemotherapy
concurrently with RTconcurrently with RT
This was interpolated in to therapy of vaginal cancer.This was interpolated in to therapy of vaginal cancer.
50. Radiation Therapy TechniquesRadiation Therapy Techniques
EBRT delivered through AP:PA portals or using 4 field “boxEBRT delivered through AP:PA portals or using 4 field “box
technique”technique”
It should ensure coverage of vagina common illiac, externalIt should ensure coverage of vagina common illiac, external
illiac, hypogastric, and obturator nodeilliac, hypogastric, and obturator node
51. Field bordersField borders
Upper border L5-S1 or L4-L5( if positive lymph nodes)Upper border L5-S1 or L4-L5( if positive lymph nodes)
( some authors 2cm above lower border of SI joint)( some authors 2cm above lower border of SI joint)
Inferior border at introitus to ensure coverage of entireInferior border at introitus to ensure coverage of entire
vagina or 4 cm distal to most caudal aspect of vaginal tumorvagina or 4 cm distal to most caudal aspect of vaginal tumor
Lateral border 1.5-2cm lateral to pelvic brimLateral border 1.5-2cm lateral to pelvic brim
Anterior- anterior to pubic symphysisAnterior- anterior to pubic symphysis
Posterior- posterior to junction of S2/S3 interspacePosterior- posterior to junction of S2/S3 interspace
52.
53. Inguinal nodes should be electively covered (4500-5000cGy)Inguinal nodes should be electively covered (4500-5000cGy)
for tumors of the lower 1/3 of vaginafor tumors of the lower 1/3 of vagina
Additional 1500cGy (4-5cm depth) delivered for palpableAdditional 1500cGy (4-5cm depth) delivered for palpable
inguinal nodesinguinal nodes
54. Radiation Therapy TechniquesRadiation Therapy Techniques
Portal for pelvic RT and
elective groin coverage
Portal for groin coverage
with palpable inguinal
nodes
56. EBRT doseEBRT dose
45-50.4 Gy IN 25-28 fractions45-50.4 Gy IN 25-28 fractions
Boost depend on size n site of lesionBoost depend on size n site of lesion
Vaginal apex > 5mm EBRT OR IBT boostVaginal apex > 5mm EBRT OR IBT boost
< 5mm - ICA< 5mm - ICA
57. Mid and distal s treated with IBTMid and distal s treated with IBT
If extensive disease treated with EBRTIf extensive disease treated with EBRT
Total dose of 70-80GyTotal dose of 70-80Gy
59. LDR ICB was performed using a vaginal cylinder loaded withLDR ICB was performed using a vaginal cylinder loaded with
Cs-137Cs-137
Usually 2-3 Cs are placed along central tandemUsually 2-3 Cs are placed along central tandem
Vaginal colpostat alone can also be used for fornicial tumorsVaginal colpostat alone can also be used for fornicial tumors
60. HDR-ICB is typically performed using Ir-192HDR-ICB is typically performed using Ir-192
EBRT 45-50.4Gy followed by HDR 20-28Gy in 3-4 fractionsEBRT 45-50.4Gy followed by HDR 20-28Gy in 3-4 fractions
63. Interstitial brachytherapyInterstitial brachytherapy
ICB not suitable > 5mmICB not suitable > 5mm
Vaginal cylinder fails to deliver sufficient coverage toVaginal cylinder fails to deliver sufficient coverage to
paravaginal tissueparavaginal tissue
Boost after EBRTBoost after EBRT
64. IBT..IBT..
Routine preoperative assessment under anaesthesia toRoutine preoperative assessment under anaesthesia to
assess diseaseassess disease
If MRI is available it s superior to assess the thicknessIf MRI is available it s superior to assess the thickness
Patient is positioned in dorsal lithotomy positionPatient is positioned in dorsal lithotomy position
A speculam and digital examination allows assessment ofA speculam and digital examination allows assessment of
vaginal width, tumor size and location, amount and thicknessvaginal width, tumor size and location, amount and thickness
of residual parametrial or paravaginal diseaseof residual parametrial or paravaginal disease
65. IBT..IBT..
A sterile set up is used at time of insertionA sterile set up is used at time of insertion
A foley catheter is placed for bladder drainageA foley catheter is placed for bladder drainage
Radio opaque markers can be kept for tumor delineationRadio opaque markers can be kept for tumor delineation
66. Templates..Templates..
Template systems are available to secure the position ofTemplate systems are available to secure the position of
needles in the target volumesneedles in the target volumes
Syed- NebletteSyed- Neblette
Modified Syed- NebletteModified Syed- Neblette
Martinez-Universal Perineal ImplantMartinez-Universal Perineal Implant
67. IBT..IBT..
These system consist of a perineal template, a vaginalThese system consist of a perineal template, a vaginal
cylinder obturator, and hollow guides for loading radionuclidecylinder obturator, and hollow guides for loading radionuclide
sources.sources.
So through opening in the template needles can be insertedSo through opening in the template needles can be inserted
Goal is to cover GTV with 1-2 cm marginGoal is to cover GTV with 1-2 cm margin
68.
69.
70. IBT..IBT..
It s optimal to place needle under image guidanceIt s optimal to place needle under image guidance
Laparoscopic. CT, USG, MRILaparoscopic. CT, USG, MRI
TRUSTRUS
With MRI n CT 3D Image based brachytherapy can be doneWith MRI n CT 3D Image based brachytherapy can be done
Increasing tumor control and decreasing toxicityIncreasing tumor control and decreasing toxicity
71.
72. Anterior localization film of an interstitial implant used to treat a deeply invasive stageAnterior localization film of an interstitial implant used to treat a deeply invasive stage
I lesion. Isodose curves representing dose rates and the tumor volume have beenI lesion. Isodose curves representing dose rates and the tumor volume have been
superimposedsuperimposed
73. Lateral localization film of an interstitial implant showing its position relative to theLateral localization film of an interstitial implant showing its position relative to the
bladder and rectum. Isodose curves representing dose rates and the tumorbladder and rectum. Isodose curves representing dose rates and the tumor
volume have been superimposedvolume have been superimposed
76. IBTIBT
HDR is preferredHDR is preferred
Limiting exposure to care givers and ability to optimize doseLimiting exposure to care givers and ability to optimize dose
distribution by 3D image based planningdistribution by 3D image based planning
Permanent implant with Au-198 n I-125 reported in elderlyPermanent implant with Au-198 n I-125 reported in elderly
patientspatients
77. Management of rare histologiesManagement of rare histologies
Small Cell CarcinomaSmall Cell Carcinoma
Poor prognosis (85% die in first year)Poor prognosis (85% die in first year)
– Reasonable local control may be obtained with surgery orReasonable local control may be obtained with surgery or
irradiation followed by systemic chemoirradiation followed by systemic chemo
– EPEP
– Cyclophosphamide, Adriamycin, Vincristine (CAV) X 12Cyclophosphamide, Adriamycin, Vincristine (CAV) X 12
cycles (some prior to initiation of RT)cycles (some prior to initiation of RT)
– Doses of RT similar to SCCADoses of RT similar to SCCA
78. ManagementManagement
RhabdomyosarcomaRhabdomyosarcoma
– Generally treated with a combination of surgery, RT, andGenerally treated with a combination of surgery, RT, and
chemotherapychemotherapy
– Vincristine, Dactinomycin, Cyclophosphamide (VAC) X 1-Vincristine, Dactinomycin, Cyclophosphamide (VAC) X 1-
2 years effective adjuvant treatment for stage 1 dz2 years effective adjuvant treatment for stage 1 dz
– Local excision + interstitial/intracavitary RT + systemicLocal excision + interstitial/intracavitary RT + systemic
chemo has replaced radical pelvic surgery as therapy ofchemo has replaced radical pelvic surgery as therapy of
choicechoice
81. ManagementManagement
Malignant LymphomaMalignant Lymphoma
< 1% of extra nodal lymphoma< 1% of extra nodal lymphoma
– Cyclophosphamide, adriamycin, vincristine, prednisoneCyclophosphamide, adriamycin, vincristine, prednisone
(CHOP) X 6 cycles most often used(CHOP) X 6 cycles most often used
– Followed by RTFollowed by RT
82. Clear Cell Adenocarcinoma andClear Cell Adenocarcinoma and
DES ExposureDES Exposure
Incidence is between 0.14 to 1.4/1000 women exposed toIncidence is between 0.14 to 1.4/1000 women exposed to
DESDES
Median age at diagnosis 19 yearsMedian age at diagnosis 19 years
Lesions found mainly in the upper 1/3 of the anterior vaginalLesions found mainly in the upper 1/3 of the anterior vaginal
wallwall
90% of patients with early stage disease (I and II) at90% of patients with early stage disease (I and II) at
diagnosisdiagnosis
83. ManagementManagement
Clear Cell AdenocarcinomaClear Cell Adenocarcinoma
– Surgery for stage I lesions has advantage of ovarianSurgery for stage I lesions has advantage of ovarian
preservation and better vaginal function following skinpreservation and better vaginal function following skin
graftgraft
– Vaginectomy, radical hysterectomy PLND, paraaorticVaginectomy, radical hysterectomy PLND, paraaortic
LNBx (frozen section of distal margin)LNBx (frozen section of distal margin)
– Intracavitary or transvaginal radiation can be used forIntracavitary or transvaginal radiation can be used for
small lesionssmall lesions
– More extensive lesions: EBRTMore extensive lesions: EBRT
85. FAVORABLE FACTORS IN SURVIVAL OFFAVORABLE FACTORS IN SURVIVAL OF
PATIENTS WITH CLEAR CELLPATIENTS WITH CLEAR CELL
ADENOCARCINOMAADENOCARCINOMA
Low stageLow stage
Older ageOlder age
Tubulocystic PatternTubulocystic Pattern
Small tumor diameterSmall tumor diameter
Reduced depth of invasionReduced depth of invasion
Negative nodal metsNegative nodal mets
Positive ho/o DESPositive ho/o DES
86. MelanomaMelanoma
Wide local excisionWide local excision
Radical surgeryRadical surgery
RadiationRadiation
Overall survival s poor 5-20%Overall survival s poor 5-20%
87. SummarySummary
Superficial stage I lesions may be treated with RT or radicalSuperficial stage I lesions may be treated with RT or radical
hysterovaginectomyhysterovaginectomy
Stage II-IVA treated with WPRT and brachytherapyStage II-IVA treated with WPRT and brachytherapy
Role of chemotherapy in advanced SCCA presentlyRole of chemotherapy in advanced SCCA presently
unknownunknown
Pelvic failures and distant metastases occur in 1/2 of pts withPelvic failures and distant metastases occur in 1/2 of pts with
advanced dzadvanced dz
The lymphatics of the vagina envelop the mucosa and anastomose with lymphatic vessels in the muscularis. Those of the middle to upper vagina communicate superiorly with the lymphatics of the cervix and drain into the pelvic nodes of the obturator and internal and external iliac chains.
60% of invasive cancer biopsy specimens and in more than 80% of patients with in situ vaginal disease, hyperkeratosis, thickening, acanthosis, and inflammation.[9] These changes may progress to metaplastic and dysplastic changes.
These lesions require multimodality therapy with surgery, chemotherapy, and radiation therapy.
most common symptom of vaginal cancer is abnormal bleeding or discharge. Pain is usually a symptom of an advanced tumor. Urinary frequency is also reported occasionally, particularly in the case of anterior wall tumors, whereas constipation or tenesmus may be
reported when the tumors involve the posterior vaginal wall. In general, the longer the delay in diagnosis, the worse the prognosis and the more difficult the therapy.
It should be noted that these numbers are specific to squamous cell lesions. In clear cell adenoca, lung and supraclavicular nodal mets represent ~35% of recurrences in young women.
Rt must be individualized in the treatment of vaginal Ca. Paravaginal and/or parametrial interstitial implants must be considered in cases with gross residual tumor after teletherapy and standard brachytherapy. The direct approximation of the vagina to the bladder, urethra and rectum makes surgical treatment difficult.
Sarcoma botryoides protruding through vaginal introitus. The tumors are believed to begin in the subepithelial layers of the vagina and
expand rapidly to fill the vagina. These sarcomas often are multicentric. Histologically, they have a loose myxomatous stroma with malignant pleomorphic cells and occasional eosinophilic rhabdomyoblasts that often contain characteristic cross-striations (strap cells).
Effective control with less radical surgery has been achieved with a multimodality approach consisting of multiagent chemotherapy (VAC), usually combined with operation. Radiation therapy has also been used.
Clear cell adenocarcinomas seen b/c of association with
intrauterine exposure to diethylstilbestrol (DES). In general, operation is the primary treatment modality because of the young age of the patients.