Ovarian Tumors of Non-Epithelial Origin and other Disorders Flashcards

1
Q

Histiogenesis of Germ Cell tumors

A
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2
Q

Dysgerminoma

Age?

Male Equivalent?

A

Young women and girls

Male equivalent is seminoma

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3
Q

Pathogenesis of Dysgerminoma

A

c-kit upregulated (diagnostic and theraputic target)

Transcription factors oct3,4, and Nanog maintain pleuripotency

Good prognosis

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4
Q

Gross Appearance of Dysgerminoma

A
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5
Q

Dysgerminoma Histopathology

A
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6
Q

Yolk Sac Tumor

Age?

Prognosis?

A

Young women <30 years of age

Good prognosis with chemotherapy

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7
Q

Gross appearance of Yolk sac tumor

A

Multiple cysts, hemorrhages

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8
Q

Diagnostic feature of yolk sac tumor

A

Increase in serum level of AFP

RICH in AFP

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9
Q

Yolk Sac tumor histopathology

A
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10
Q

Choriocarcinoma is identical to what?

A

Placental tumor

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11
Q

Choriocarcinoma course/timeline

A

Primary tumor may regress, leaving only metastasis sites

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12
Q

Types of epithelium involved in Choriocarcinoma

A

Syncytiotrophoblast

Cytotrophoblast

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13
Q

Choriocarcinoma gross appearance

A

Small hemorrhagic nidus/focus

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14
Q

Types of Ovarian teratomas?

A

Mature (benign, cystic (dermoid cyst))

Immature Teratoma

Monodermal (specialized)

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15
Q

Mature Teratoma

A

all three germ ayers

commonest germ cell tumor

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16
Q

Immature Teratoma

A

potentially malignant

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17
Q

Monodermal Teratoma

A

Struma ovarii

ovarian carcinoid

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18
Q

Mature Cystic Teratoma

Age?

A

Any age, usually younger patients

In elderly women–> might see malignant transformation (squamous cell carcinoma)

19
Q

Mature Cystic Teratoma gross appearance

A

Mature tissues haphazardly arranged

Hair, teeth, and sebaceous glad

Mature NORMAL tissue, haphazardly arranged. Mostly, Hair, teeth and csebaceous glands. But cartilage and intestinal epithelium may also be seen.

20
Q

Immature Teratoma

Age?

A

Prepubertal adolescents and young women

21
Q

Complication of immature ovarian teratoma

A

Potentially malignant

22
Q

Derivation of immature teratoma

A

immature neural tissue

23
Q

Two types of monodermal (specialized) teratoma

A

Struma Ovarii

Ovarian Carcinoid

24
Q

Complication of Struma Ovarii

A

thyrotoxicosis

25
Complication of ovarian carcinoid
carcinoid syndrome
26
Types of Sex chord stromal tumors
Granulosa cell tumor thecoma fibroma sertoli-leydig cell tumor gonadoblastoma
27
Granulosa cell tumor Gross
Solid, yellow, small cysts
28
Granulosa cell tumor Histopathology
29
Fibromas, thecomas, and fibrothecomas Benign or Malignant?
BENIGN
30
Thecoma Histology and Marker
Histo= theca cells Marker= estrogen
31
Thecoma estrogen excess complication?
Dysfunctional uterine bleeding Endometrial hyperplasia and carcinoma
32
Thecoma Gross appearance? Thecoma histological appearance?
Gross: Pale fleshy cut surface, yellowish fatty areas Histopathology: Spindle cells with abundant lipid
33
Fibroma?
Histologically, MEIGS Syndrome may be seen with the benign ovarian tumor may be a fibroma, thecoma, cystadenoma, or granulosa cell tumor. Fibromas are also associated with Benign Nevus syndrome.
34
Sertoli-Leydig cell tumor malignant or benign?
malignant
35
Sertoli Leydig cell tumors secrete what?
May secrete Androgens | (Virilization or defeminizing symptoms)
36
Sertoli Leydig cell tumor Gross? Histo?
37
Granulosa Cell tumor marker?
INHIBIN
38
Gonadoblastoma characteristic feature?
Dysgenic streak ovaries (Germ cell component may undergo malignant change to form Dysgerminoma AND Granulosa cells)
39
Primary sites for metastatic tumors?
Primary sites: breast \> colon \> endometrium \> stomach
40
Metastatic tumor characteristics?
B/L, solid Histologically- adenocarcinoma
41
What is a Krukenberg tumor?
Bilateral metastases of mucin-producing signet-ring cell carcinoma within the ovarian stroma Bilateral fleshy cerebriform masses
42
Krukenberg Tumor histo?
Clusters of Signet Ring Cells
43
Where does Krukenberg tumor originiate from (What metastasizes)?
Metastasis from Gastric carcinoma
44
Pathological Basis of signs and symptoms in the reproductive age female?