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Cancer of the Vulva Essentials of Diagnosis • Typically occurs in postmenopausal women. • Long history of vulvar irritation with pruritus, local discomfort, and bloody discharge. • Appearance of early lesions like that of chronic vulvar dermatitis. • Appearance of late lesions like that of a large cauliflower, or a hard ulcerated area in the vulva. • Biopsy necessary for diagnosis. Types of Vulvar Cancer • Squamous Cell Carcinoma- most common type of tumor (85-90%) and most frequently involves the anterior half of the vulva. • Malignant Melanoma- second most common vulvar cancer (5%) • Carcinoma of Bartholin's Gland- most common site for vulvar adenocarcinoma • Basal Cell Carcinoma- arise almost exclusively in the skin of the labia majora Squamous Cell carcinoma • 65% arises in labia majora and minora • 25% percent in clitoris or perineum • Appearance varies from a large, exophytic, cauliflowerlike lesion to a small ulcer crater superimposed on a dystrophic lesion of the vulvar skin • primary determinant of nodal metastases is tumor size. Malignant Melanoma • Accounts for 5% of vulvar cancers • most commonly arises in the labia minora and clitoris • superficial spread toward the urethra and vagina • nonpigmented melanoma may closely resembles squamous cell carcinoma • darkly pigmented, raised lesion is a characteristic finding • All small pigmented lesions of the vulva are suspect and should be removed by excision biopsy with a 0.5- to 1-cm margin of normal skin • large tumors, the diagnosis should be confirmed by a biopsy Carcinoma of Bartholin's Gland • Rare (1%) but the most common site of vulvar adenocarcinoma • Most common type is squamous cell metastasis • Primarily lymphatics to the superficial inguinal lymph nodes • Direct extension to vagina, urethra and anus Treatment • TOC: wide local excision with inguinal lymph node metastasis • Stage I: ipsilateral lymphadenectomy • Stage II and III: bilateral lymphadenectomy • Late stage III and IV: radical vulvectomy, lymphadenectomy and/or chemoradiation Cancer of the Vagina • Rare, approximately 3% of gynecologic cancers • Squamuos cell(85%)>adenocarcinomas> sarcomas>melanomas. • Can be ulcerative or exophytic Essentials of Diagnosis • Asymptomatic: abnormal vaginal cytology. • Early: painless bleeding from ulcerated tumor. • Late: bleeding, pain, weight loss, swelling. Endometrial Cancer • 3rd most common gynecologic malignancy in the Philippines • Affects mostly peri/postmenopausal women RISK FACTORS: Estrogen replacement therapy 4-8x Menopause after 52 years 2.4x Obesity 3x-21 to 50lbs, 10x->50lbs Nulliparity 2-3x Diabetes 2.8x Feminizing ovarian tumors Polycystic ovarian syndrome Tamoxifen therapy for breast cancer >2 years • • • • • • • Protective factors: Ovulation Progestin therapy Combination oral contraceptives Menopause prior to 49 years Normal weight Multiparity • Etiology: unopposed estrogen exposure • Clinical presentation: Abnormal uterine bleeding (80) Physical exam ussually unremarkable Staging FIGO Surgical Staging of Carcinoma of the Corpus Uteri • Stage I • Stage Ia G123 Tumor limited to endometrium • Stage Ib G123 Invasion to less than one-half the myometrium • Stage Ic G123 Invasion to more than one-half the myometrium • Stage II • Stage IIa G123 Endocervical glandular involvement only • Stage IIb G123 Cervical stromal invasion • Stage III • Stage IIIa G123 Tumor invades serosa and/or adnexa, and/or positive peritoneal cytology • Stage IIIb G123 Vaginal metastases • Stage IIIc G123 Metastases to pelvic and/or paraaortic lymph nodes • Stage IV • Stage IVa G123 Tumor invades bladder and/or bowel mucosa • Stage IVb Distant metastases including intra-abdominal and/or inguinal lymph nodes • Treatment • Primary: surgery bilateral salpingo-oophorectomy, peritoneal washings for cytology, and removal of pelvic and periaortic lymph nodes • Adjuvant Chemotherapy: for advanced stages Doxorubicin and cisplatin Cancer of the Ovary • Epithelial -65% • Germ cell- 20-25% • Sex cord-6% • Etiology =frequent ovulatio n • Risk factors=nullipairty, decreased fertility, early and late menopause, ovulatory drugs Clinical presentation • • • • Asymptomatic until late stage Enlarging abdomen, abdominal mass Urinary frequency, dysuria, GI complaints Metastasis to the umbilicus is known as Sister Mary Joseph Nodule Epithelial Ovarian Cancer • • • • • SEROUS - most common type MUCINOUS ENDOMETRIOID CLEAR CELL BRENNER Management • SURGERY- primary management • CHEMOTHERAPY▫ Paclitaxel-Carboplatin 6 cycles every 3-4 weeks • CA-125- elevated in 80% of px with ovarian Ca -use to evaluate treatment Germ cell Tumors • 20-25% of ovarian cancers • Arises from undifferentiated germ cells Histologic Classification • Dysgerminoma- most common malignant GCT • Teratoma- most common GCT • Endodermal sinus tumor • Embryonal carcinoma • Polyembryoma • Choriocarcinoma • Mixed forms Serum Tumor Markers for Germ Cell tumor hCG AFP LDH CA-125 Neoplasis dysgerminoma Mixed germ cell tumor + + Embryonal Carcinoma + + Endodermal sinus + + + + + + Clinical manifestation • • • • • Tumors grow rapidly Distention of the ovarian capsule Hemorrhage Pelvic pain Pressure on rectum or bladder Treatment • Unilateral salpingo-oophorectomy • Sensitive to chemotherapy- bleomycin, etoposide, cisplatin (BEC) • Dysgerminomas- radiation theraPY • SURVIVAL RATE(5 year): • Dysgerminomas-85% • Immature teratomas-70 to 80% • Endodermal sinus tumors- 60 to 70% Sex Cord-Stromal Tumors • • • • • Low-grade malignancies Occur at any age Usually unilateral and do not often recur Functional tumors- produced hormones Granulosa-theca cells: large amounts of estrogens • Sertoli-Leydig cells: testosterone and androgens Granulosa-theca cell tumors • • • • • Precocious puberty Menstrual irregularities Secondary ammenorrhea Post-menopausal bleeding Endometrial hyperplasia and/or endometrial cancer Sertoli-Leydig Cell tumors • Virilization: breast atrophy, hirsutism, deepened voice, acne, clitoromegaly and receding hairline • Oligomenorrhea or amenorrhea treatment • Unilateral salpingo-oophorectomy • Chemotherapy- not effective 5 year survival rate: 70-90% Fallopian Tube Cancer • Extremely rare: 0.5% of genital tract cancers • 80-90% of FT malignancies are metastatic from other sites (ovary, uterus, GIT • Unknown etiology • Hereditary association (BRCA1) Clinical manifestation • Hydrops tubae profluens: profuse watery discharge, pelvic pain and pelvic mass - Classic triad of fallopian Ca, only 15% of cases, pathognomonic Treatment • TAHBSO, retriperitoneal lymph node sampling • Carboplatin and paclitaxel- adjunct therapy