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1. Epithelial stromal tumor cell typesa. serous
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1. NEOPLASTIC DISEASES OF OVARYDr. Cayabyab Ovarian neoplasm 2nd most malignant in female genital tract
Classification of ovarian neoplasm
1. epithelial stromal 65%
2. Germ Cell tumors 20 -25 %
3. Sex Cord Stroma 6%
4. Lipid cell tumor <0.1%
5. Gonadoblastoma <0.1%
Others: soft tissue, unclassified, metastatic, tumor- like
2. 1. Epithelial stromal tumor cell types
a. serous most common
b. mucinous
c. endometroid
d. clear cell
e. Brenner
Epithelial can be categorized as
benign (adenoma)
malignant(adenocarcinoma)
intermediate- borderline/tumors of low malignant potential
3. Associations of increasing or decreasing risks of ovarian epithelial carcinoma
Increases Decreases
1. age breastfeeding
2. diet OCP
3. family history pregnancy
4. industrialized tubal lig/hyst
country conserve ovary
5. infertility
6. nulliparity,ovulation
ovulatory drugs/talc?
4. Benign conditions in which Ca -125 is increased:
1. endometriosis
2. peritoneal inflammation
3. Leiomyoma
4. pregnancy
5. hemorrhagic ovarian cyst
6. liver disease
Ca-125 is the tumor marker in ovarian neoplasm
5.
Staging of ovarian Ca
Stage 1- growth limited to ovaries
1A one ovary no ascites capsule intact
1B both ovaries no ascites
1C either 1A or 1B capsule ruptured
ascites + / peritoneal washing +
6.
Stage 11 one or both ovaries with pelvic extensions
11A mets to uterus/ tubes
11B - mets to pelvic tissues
11C either 11A/11B
capsules ruptured
+ascites
+ peritoneal washings
7. Stage 111 one or both ovaries with peritoneal implants outside the pelvis
+ retroperitoneal/inguinal nodes
superficial liver mets
limited to true pelvis
histologically proven malignant extension
to small bowel or omentum
111 A- limited to true pelvis /microscopic seeding
111 B one or both ovaris with implants
none exceeding 2 cm, nodes negative
111C abdominal implants more than 2cm
(+) retroperitoneal/inguinal nodes
8.
Stage 1V one or both ovaries with distant mets if pleural effusion present
there must be (+) cytology
1VA parenchymal liver mets
9. Diagnosis:
Pelvic exam- palpation of a mass
USG usually incidental
Dx frequently made after the disease had spread beyond the ovary
Pt manifest
ascites
vague abdominal discomfort
swollen abdomen first sign
confirmatory dx histopath after the ovarian tissue was removed surgery.
others: CT scan , CA -125
10. Staging of ovarian ca is based on the result of operative exploration.
Spread extension lymphatic
Management Explore lap
childbearing preserve one ovary
chemotherapy
Prognosis: depends on
Stage
Grade
cell type
amount of residual tissue
11. 2. Germ Cell tumors - second most frequent
1. Dysgerminoma
a.endodermal sinus tumor
b. embryonal ca
c. polyembryoma
d.choriocarcinoma
e. teratomas
immature
mature - solid/cystic
12. Mature
dermoid cyst ( mature cystic teratoma)
dermoid cyst with malignant transformation
Monodermal and highly specialized
struma ovarii thyroid tissue
carcinoid GIT tissue
sruma ovarii/carcinoid
Others
Mixed forms
13. Mature Teratomas
has 3 layers of developing embryo
Ectoderm
Mesoderm
Endoderm
has XX karyotype
Benign cystic teratomas (Dermoids)
most common germ cell tumor
more on reproductive years
usually unilateral
14. Immature teratomas malignant
Dysgerminoma- has primitive germ cells with stroma infiltrated with lymphocytes
radiosensitive
usually bilateral
Endodermal sinus tumor (yolk sac tumor
has Schiller duval bodies
secretes alpha feto protein
common in young patients
15. Gonadoblastomas with germ cell and sex cord stromal elements
Granulosa theca cell tumors with granulosa cells
has Call Exner bodies
pt may manifest vaginal bleeding
more in older patiets
Thecomas/ fibromas
thecomas benign solid
in menopause
16. Fibromas can have large ovarian tumor with asictes/ pleural effusion
hydrothorax(Meigs syndrome)
regress upon removal of tumor
Metastatic- tumors
Krukenburgs tumor
tumors from GIT