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17 Cards in this Set

  • Front
  • Back
What percentage of ovarian malignancies are sex-cord-stromal tumours?
5%
List histological subtypes of SCSTs
Granulosa-Stromal Cell tumours
granulosa cell
fibroma
thecoma
Androblastomas
Sertoli
Sertoli-Leydig
Leydig
Benign or malignant:

a) Granulosa-cell tumour
b) Fibroma
c) Thecoma
a) low-grade malignant
b) benign
c) benign

(b&c can rarely have malignant features - fibrosarcomas)
List two serum "markers" of granulosa cell tumours.
Estradiol
Inhibin

MIS, mullerian inhibitory substance, is an experimental marker for GCT
In post-menopausal women, what is the rate of endometrial:

a) hyperplasia
b) cancer

associated with a concurrent GCT?
a) 25-50%
b) 5%
a) What is the typical prognosis of SCSTs?

b) What age groups are primarily affected?
a) Excellent - majority diagnosed in Stage I and generally of low malignant potential/indolent growth pattern.

b) all age groups
What is Meig's syndrome?

What is pseudo-Meig's syndrome?
a) Ovarian Fibroma, Ascites, Pleural effusion (classically right-sided)

b) Ovarian Fibroma, Ascites, Pleural effusion (classically right-sided)

b) Non-fibroma ovarian/adnexal mass, Ascites, Pleural effusion (classically right-sided)
What hereditary syndromes can be associated with SCSTs?
Peutz-Jeghers syndrome
Ollier disease
How do SCSTs typically present?
Abdomino-pelvic mass/pain

Precocious puberty (premenarche)
Amenorrhea
PMB (menopausal)
For SCSTs, which subtypes develop from the coelomic epithelium (sex-cords)?

Which develop from the mesenchyme (stroma)?
a)
Granulosa cell
Sertoli

b)
Fibroma
Leydig
Theca
What is the natural history of SCSTs?
Low malignant potential
Usually unilateral
Typically diagnosed Stage I
5yr survival 90-95%
Relapses can happen 5-30 yrs later
typically in the pelvis or abdomen, focally

Stage II-VI at diagnosis carries worse prognosis
10-50% 5yr survival
a) Describe the two different types of granulosa cell tumour:

b) What is the specific histocytological finding?
a)
Adult (95%)
Juvenile (5%)

b) Call-Exner Body
What hormone do thecoma's usually produce?
Estrogen

(since they typically develop in menopausal women, they are strongly associated with PMB and endometrial hyperplasia/cancer).
What ovarian SCSTs produce androgens?
Sertoli-Leydig
Leydig
What is the histocytological finding in Leydig tumours?
Crystals of Reinke
Management of SCSTs is primarily based on:
Initial cytoreductive surgery +/- staging
Surgery can be fertility sparing or TAH/BSO
Surveillance vs Chemo/Radiation
a) What prognostic factors can be used to decide if Stage I SCST should be treated with post-op adjuvant chemotherapy?

b) When should post-op adjuvant chemotherapy be offered/recommended?
a)
Size
Age
Mitotic Index
Tumour Rupture
Capsular excrescences

b)
Stage >= II or those with risk factors as above