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25 Cards in this Set
- Front
- Back
PID Casues
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– most polymicrobial
– N. gonorrhea most common single, upward migration from mucinous glands gets tubo-ovarian region – also E. coli, Staph, Strep, Clostridium via lymph or vascular after surgery – Also Chlamydia, Mycoplasma, Actinomyces (IUDs) |
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Adenomatoid tumor
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benign fallopian tumor of mesothelial origin
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Surface epi inclusion cysts of ovaries
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small cysts from involution of surface epi, benign
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Functional ovarian cysts
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follicular and corpus luteal cysts, benign
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PCO path
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– Increased ovarian production of androgens that act locally to cause premature follicular atresia, multiple follicular cysts, persistent anovulatory state and decreased P
– Excess androgens converted to E in peripheral adipose tissue |
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Sporadic ovarian cancer
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– activation of oncogenes (c-myc, K-ras, HER2/neu)
– Inactivation of tumor suppressor genes (p53, p16) – Aneuploidy |
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Hereditary ovarian cancer
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– 5-10% in women w/ familial susceptibility to ovarian and/or breast cancer
– Germline mutations in DNA repair genes – BRCA-1 (chromo 17), BRCA-2 (chromo 13) |
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Most common germ cell tumor in adults
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95% are benign mature cystic teratomas (dermoid cyst)
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Ovarian mets
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– stomach (Krukenberg tumor) colon, pancreas and appendix
– also breast, endometrium |
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Ovarian tumor cell markers
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– Serous/endometrioid is CA125
– Mucinous is CEA – Yolk sac tumor is AFP – Choriocarcinoma is hCG |
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Imperforate hymen
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– no obvious vaginal orifice
– thin, bulging, blue perineal membrane – fluctuant pelvic |
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Mullerian agenesis
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– Absent vagina, absent/ rudimentary uterus
– 46,XX, – Normal ovaries – Normal 2o sexual development – ASx |
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Transverse vaginal septum/cervical atresia
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– Blind vaginal pouch, 46,XX
– Normal ovaries – Normal 2o sexual development – Cryptomenorrhea |
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Asherman Syndrome
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– Synechiae
– Dx w/ strong suspicion – based on hx uterine curettage (retained POC, endometritis) – hx of IUD infection or PID – hx of genital TB, schistosomiasis – Hysterosalpingogram (HSG) |
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Drugs that could cause amenorrhea
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Phenothiazines
Reserpine Amphetamines Opiates Benzos Butyrophenones TCA’s Metaclopramide |
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Enzyme deficiencies that can cause ammenorhea w/ high FSH
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P450c17, aromatase
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Evaluation for PCOD
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– 1) T (producing neoplasm) > 200 – Transvaginal U/S – Adrenal CT/MRI
– 2) 17-hydroxyP (nonclassical CAH) > 2 – ACTH stim test – 3) 24 hr cortisol if cushing signs and Sx |
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Abnormal Uterine bleeding Evlauation
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– 1) Exclude pregnancy
– 2) Identify anemia, thrombocyto – 3) Assess ovulatory function – Menstrual hx, Timed serum P, Endometrial bx (Age > 40 yr – Hx of chronic anovulation – Confusing/suspicious hx) |
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Hypoestrogenism
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– Thin, inactive endometrium
– don’t tx w/ P, b/c it organizes and attenuates bleeding – Dx if Biopsy yields minimal tissue and there is Attenuated endometrium (Stripe < 4 mm) – Tx must begin w/ estrogen to build a foundation, then do progestin |
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Why is nulliparity an RF for endometrial cancer
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– Infertility common link
– Anovulation – high serum levels of androstenedione – lack of monthly menses more common in this population |
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Endometrial cancer and ultrasound
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– Normal has a very thin lining
– if lining less than 5 mm, possibility of having endometrial cancer is very small – if asian, less than 3 means you are ok |
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Endometrial Cancer Staging
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– Stage I is Uterus only
– Stage II is Cervical involvement – Stage III is Ab involvement (tubes/ovaries/washings/nodes) or vaginal involvement – Stage IV is Bowel, bladder, or mets |
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First line Tx for ovarian cancer
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– Debulking Surgery/Staging
– then Chemotherapy (Platinum + Taxol) every 3 weeks for 6 cycles – then second look surgery |
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2nd line Tx for ovarian cancer
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– Ovarian cancer recurrence
– then Other chemo? Hormonal treatment? Interval debulking surgery? Radiation |
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Ovarian Cancer Staging
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– Stage I is Ovaries only
– Stage II is Pelvic extension – Stage III is Abdominal implants or lymph node spread – Stage IV is Distant METs |