Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
42 Cards in this Set
- Front
- Back
condyloma accuminata
|
wartlike lesions, vulva, vagina, cervix.
assoc. w/ HPV 6, 11. Mic: Koilocytosis: vacuolization around nucleus, acanthosis, hyperkeratosis, parakeratosis |
|
Papillary hidradenoma
|
benign tumor, along milk line, histo similar to intraductal papilloma.
|
|
Extramammary Paget Dz of vulva
|
usually labia majora
Micro: intraepidermal malignant cell with pagetoid cells |
|
Vaginal adenosis and clear cell carcinoma of vagina
|
Rare, assoc w/ DES exposure in utero
|
|
Sarcoma botryoides (embryonal rhabdomyosarcoma (vagina)
|
infants and children
gross: poypoid, "grape like" soft tissue protruding from vagina Micro: cells with cross-striations (strap cells). grow underneath vaginal epithelium. POS for "desmin" marker! |
|
PID (cervix)
|
ascending infection, usually STD (gonorrhea and/or chlamydia).
Endometritis, salpingitis, pelvic abscess |
|
Fitz-Hugh-Curtis Syndrome
|
aka perihepatitis, characterized by violin-string adhesion between fallopian tube and the liver capsule SEEN IN PID.
|
|
Complications of PID
|
tubo-ovarian abscess, tubal scarring resulting in infertility and ectopic tubal preg. Also intestinal obstruction
|
|
Icidence of Cancer
|
Endometrial > Ovarian > Cervical
|
|
Mortality
|
Ovarian > endometrial > cervical
Cervical number one in the world. |
|
Cervical carcinoma
|
Risky behavior (sex) of contracting HPV, smoking, STD's, immunosupression.
Peaks in the 40's. |
|
HPV
|
High risk ones are Type 16, 18, 31, 33, 45.
E6 binds p53 E7 binds Rb |
|
Progression of Cervical Squamous cell carcinoma
|
CIN (cervical Interaepithelia Neopplasia): CIN I (mild dysplasia), CIN II: moderate, CIN III Severe, CIS (in situ) and then invasion of basement membrane.
|
|
Cervical Cancer: Clinical presentation
|
Postcoital (after sexual untion) vaginal bleeding, pain during intercourse (dyspareunia), malodorous discharge, or asymptomatic.
|
|
Endometritis
|
Chronic: PLASMA cell in endometrium (should not be normally there). Assoc w/ PID, IUDs etc.
Acute: ascending infection from cervix, preg, abortion. |
|
Endometriosis
|
presence of endometial stroma and glands outside the uterus. commonly in ovary, pouch of douglas behind uterus,.
Gross: ovarian "CHOCOLATE" cyst. red brown serosal nodules: "poweder burn". |
|
Endometriosis: clinical presentation
|
chronic pelvic pain, dysmenorrhea, dyspareunia, infertility, rectal pain, constipation.
|
|
Leiomyoma (fibroids)
|
most common tumor of genital tract in females.
Huge in African Americans. responsive to Estrogen. "rubbery white tan appearance, well circumcised, multiple". "Whorl-like trabeculated appearance on cut section." may goto Leiomyosarcoma |
|
Endometrial carcinoma
|
Most common malignant tumor. common in POST-MENOPAUSAL females.
risk factors: nulliparity, obesity, estrogen RT, tamoxifen, E2 producing ovarian tumors (granulosa cell tumors).// |
|
Lynch Syndrome
|
colon, endometrial and Ovarian cancers.
|
|
Endometrial carcinoma: gross and CP
|
Clin Presentation: Post-menopausal bleeding.
Gross: polypoid, TAN Most common type: Endometriod adenocarcinoma |
|
Polycystic Ovarian Dz
|
aka Stein-Leventhal Syndrome
benign, bilateral, follicular cysts. young female, oligo, amenorrhea, hirsuitism, infertility, obesity. Lab: high LH, Low FSH, High Testosterone Tx: with BC or Provera |
|
Epithelial Ovarian Tumors
|
Most common form of Ovarian tumor.
1. Cystadenoma: benign, unilocular, simply serous or mucous. can be MASSIVE 2. borderline tumors: low malignant potential 3. Cystadenocarcinoma: most common malignant ovarian tumor. |
|
Cystadenocarcinoma
|
complex multioculated cysts, nodular and solid areas.
Micro: papillary structures with PSAMOMMA BODIES, stromal invasion. Spread via seeding peritoneal cavity. |
|
Heridatary risk factors: cystadenocarcinoma of ovary
|
BRCA-1, Lynch Syndrome
Marker: **CA 125**. Presenation: vague, late presenation |
|
Ovarian Germ cell tumors
|
Teratoma, Dysgerminoma, Yolk sac tumor, choriocarcinoma
|
|
Teratoma of ovary
|
aka dermoid cysts. Have all three germ cell components, mostly benign, common in younger women.
May have hair, teeth, bone, cartillage etc. |
|
Struma Ovarii
|
preponderonce of thyroid tissue in teratoma, causes hyperthyroidism
|
|
immature teratoma
|
some elements are immature and is troublesome because it can become malignant via transformation.
|
|
Complications: teratoma
|
torsion, rupture, malignant tranformation (1%) usually SCC.
|
|
Dysgerminoma
|
female equivalent of seminomas.//
young adults, radiosensitive. High risk in: Turner syndrome, pseudohermaphrodites.// |
|
Ovarian Sex-cord stromal tumors
|
ovarian fibroma, granulosa cell tumor, sertoli-leydig cell tumor (androblastoma)
|
|
Ovarian fibroma
|
firm, WHITE masses, most common stromal tumor
may present as Meigs syndrome |
|
Meig syndrome
|
fibroma + ascites + pleural effusion (right-sided)
|
|
Granulosa cell tumor
|
potentially malignant, CAN PRODUCE ESTROGEN.
precocious puberty, irregular cycles, Postmenopausal; bleeding again. Gross: YELLOW white mass. Micro: polygonal tumor cells, follicle like structure (CALL-EXNER BODIES) complication: endometrial hyperplasia, and cancer. |
|
sertoli-leydig cell
|
ANDROGEN producing., risk of pseudohermaphrodite offspring, virilization
|
|
Metastatic tumors of ovary
|
KRUKENBERG tumor: a metastatic carcinoma of the ovary, usually bilateral and secondary to a mucous carcinoma of the stomach, which contains signet-ring cells filled with mucus.breast, colon, endometrial.
|
|
Gestational Trophoblastic Disease
|
Hydatidiform mole (molar pregnancy), invasive moles, choriocarcinoma.
|
|
Hydatidiform Mole (molar pregnancy)
|
tumor of trophoblastic (placental) tissue.
Result from fertilization of an ovum that has lost all of its chromosomes. at extremes of reproductive life, higher in Asia than US CC: Size greater than dates (uterus), vaginal bleeding, passage of grapelike soft tissue Micro: edematous chorionic villi, trophoblast proliferation, fetal tissue (in partial mole) Tx; curettage, follow with beta hCG levels. about 1 in 1000 pregnancies. |
|
Complete Mole
|
diploid, 46 all paternal chromosomes, elevated hCG, NO fetal tissue, 2% to choriocarcinoma.
|
|
Partial Mole
|
69 chromosomes (23X maternal, 23X one sperm, 23Y the other sperm) XXY (triploid cells)
somewhat elecated hCG, fetal tissue present, rarely goes to choriocarcinoma. |
|
Choriocarcinoma
|
most malignant tumor in humans, derived from trophoblast
Responsive to chemotherapy Hematogenous spread to lungs, brain and liver etc. |