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30 Cards in this Set

  • Front
  • Back
1. From what are ovarian epithelial tumours derived?
a. From ovarian epithelium and account for 90% of ovarian cancers.
2. Presentation of ovarian epithelial tumours?
a. Slow-growing so most pts are asymptomatic or may have non-specific vague complaints.
b. Therefore 75% of pts are diagnosed at stage III or higher.
3. Symptoms of ovarian epithelial tumours when present?
a. Low abdominal pain
b. Bloating
c. Early satiety
d. Pelvic mass and ascites
a. Low abdominal pain
b. Bloating
c. Early satiety
d. Pelvic mass and ascites
1. Pelvic U/S
2. Abdominopelvic CT
b. These may reveal a fixed, solid, nodular mass.
5. How are epithelial Ovarian Cancers staged?
a. Surgically.
b. Stages I:IV.
6. Stage Ia, Ib, and IC Ovarian carcinoma?
a. Stage I: Growth limited to ovaries
b. Ia: 1 ovary involved
c. Ib: Both ovaries involved
d. Ic: Ia or Ib and ovarian surface tumour, ruptured capsule, malignant ascites, or peritoneal cytology positive for malignant cells.
7. Stage IIa, IIb, IIc ovarian carcinoma?
a. Stage II: Disease extension from the ovary to the pelvis.
b. IIa- Extension to the uterus or fallopian tube
c. IIb- Extension to other pelvic tissues
d. IIc- IIa or IIb and ovarian surface tumour, ruptured capsule, malignant ascites, or peritoneal cytology positive for malignant cells.
8. Stage IIIa, IIIb, IIIc ovarian carcinoma?
a. Stage III: Disease extension to the abdominal cavity
b. IIIa- abdominal peritoneal surfaces w/microscopic mets.
c. IIIb- Tumour mets >2 cm in size.
d. IIIc- Tumour mets >2 cm in size or metastatic disease in the pelvic, para-aortic, or inguinal lymph nodes.
9. Stage IV ovarian carcinoma?
a. Malignant pleural effusion
b. Pulmonary parenchymal mets
c. Liver or splenic parenchymal mets (not surface implants)
d. Mets to the supraclavicular lymph nodes or skin.
10. Tx of Ovarian carcinoma?
a. Surgery:
1. TAHBSO
2. Omentectomy
3. Pelvic and aortic LN sampling
4. Cytoreduction
b. Followed by Taxol or carboplatin chemotherapy.
11. Tumour marker used to evaluate the success of tx and look for recurrence of disease in Ovarian Cancer?
a. CA-125.
12. 5-year survival for epithelial ovarian cancer?
a. <20%.
13. From what do Germ cell tumours arise?
a. From totipotential germ cells capable of differentiating into yolk sac, placental or fetal tissues.
14. What % of germ cell tumours are benign and malignant?
a. 95% are benign
b. 5% are malignant
15. Most common germ cell tumour?
a. Benign mature cystic teratoma (dermoid cyst).
16. 2 Most common malignant germ cell tumour?
a. Dysgerminomas (50%)
b. Immature teratomas (20%)
11. Tumour marker used to evaluate the success of tx and look for recurrence of disease in Ovarian Cancer?
a. CA-125.
17. In what age group do germ cell tumours occur?
a. Primarily in women <20.
12. 5-year survival for epithelial ovarian cancer?
a. <20%.
18. Growth characteristics of germ cell tumours?
a. Grow rapidly and are usually diagnosed at early stages.
b. Usually unilateral
13. From what do Germ cell tumours arise?
a. From totipotential germ cells capable of differentiating into yolk sac, placental or fetal tissues.
19. Tumours markers produced by germ cells tumours?
1. LDH
2. AFP
3. hCG
b. These can be used in the diagnosis of a pelvic mass and to assess response to therapy.
14. What % of germ cell tumours are benign and malignant?
a. 95% are benign
b. 5% are malignant
20. How are most germ cell tumours treated?
a. By removal of the affected ovary, staging, and combination chemo.
15. Most common germ cell tumour?
a. Benign mature cystic teratoma (dermoid cyst).
16. 2 Most common malignant germ cell tumour?
a. Dysgerminomas (50%)
b. Immature teratomas (20%)
17. In what age group do germ cell tumours occur?
a. Primarily in women <20.
18. Growth characteristics of germ cell tumours?
a. Grow rapidly and are usually diagnosed at early stages.
b. Usually unilateral
19. Tumours markers produced by germ cells tumours?
1. LDH
2. AFP
3. hCG
b. These can be used in the diagnosis of a pelvic mass and to assess response to therapy.
20. How are most germ cell tumours treated?
a. By removal of the affected ovary, staging, and combination chemo.