ovarian pathology Flashcards

(53 cards)

1
Q

non-neoplastic cysts

A

follicular cysts
corpus luteum cyst
endometriosis

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2
Q

follicular cysts

A
very common reach up to 5cm
forms when there is no LH surge and cyst doesn't rupture to release egg
usually harmless
resorb in 2-3 cycles
smooth walled unicameral/simple cysts
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3
Q

corpus luteum cyst

A

if the opening from the released egg seals -> cyst
may spontaneously resolve or grow to 4cm
may hemorrhage or undergo torsion

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4
Q

endometriosis

A

repeated cycles may form chocolate cyst

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5
Q

ovarian torsion

A

sudden unilateral pain
occurs in young adult women typically with mass >5cm
must R/O ectopic by ultrasound
surgery

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6
Q

PCOD

A

aka stein-leventhal syndrome
most common endocrine issue in repro age women
8-10% of all women worldwide

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7
Q

PCOD symptoms

A

oligomenorrhea
hyperandrogenism (hirsutism etc)
polycystic ovareis
obesity, acanthrosis nigricans, DM, premature atherosclerosis

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8
Q

features of PCOD

A
anovulation
MMR (amenorrhea)
infertility
acne, hirsuitism
insulin resistance and obesity 
high cholesterol
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9
Q

stromal hyperthecosis

A

overlaps with PCOD
usually both ovaries enlarged with hormonally active ovarian stroma
most common in postmenopausal
virulization may be striking

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10
Q

infertility

A

failure to conceive after 1 year of sex

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11
Q

fecundity

A

likelihood of pregnancy over time

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12
Q

serous tumors

A

47%
cystadenoma
borderline tumors
adenocarcinomas (type I and II)

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13
Q

mucinous tumors

A

3%
cystadenoma
adenocarcinoma (only type I)

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14
Q

endometrioid tumors

A

20%

adenocarcinomas (type I and II)

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15
Q

sex-cord stromal tumors

A

granulosa tumors
fibrothecomas
sertoli-leydig tumors

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16
Q

germ cell tumors

A

teratoma
dysgerminoma
endodermal
sinus (yolk sac)

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17
Q

metastatic tumors

A

5%

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18
Q

ovarian CA overview

A
asymptomatic until late
disease of older women (60s)
BRCA 1&2 mutations
lynch syndrome II (MSH 2 mutation)
prognosis dependent on stage
often b/l
NO effective screening
may arise from distal fallopian tube
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19
Q

serous cystadenoma

A

common benign lined by single layer of epi which is ciliated

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20
Q

serous borderline carcinoma

A

excrescences on cyst wall, more cytologic atypia, NO invasion
papillary
often seed peritonium
100% 5 yr survival

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21
Q

serous adenocarcinoma type I

A

low grade slow progression

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22
Q

serous adenocarcinoma type II

A

presents late

worse prognosis

23
Q

psammoma bodies

A

pathogmonic for serous adenocarcinoma (not specific for either type)

24
Q

mucinous tumors

A

least likely to be b/l (if it is R/O mets)
80% benign
KRAS mutation

25
rupture of mucinous tumors
pseudomyxoma peritonei -mucinous ascites w/mets on peritoneal surfaces usually d/t appendix rupture
26
endometrioid tumros
mostly carcinomas may arise in endometriosis 30% concurrent ovarian and endometrial endometrioid carcinomas
27
type I endometrioid tumors
PTEN and KRAS
28
type II endometrioid tumors
p53 CDH1 MI
29
high-grade serous immunoprofile
``` p53+ WT1+ Pax8+ High Ki67 2/3s are ER+ ```
30
high-grade serous mutation
tp53 | BRCA1,2
31
low-grade serous immunoprofile
WT1+ Pax8+ p53- low Ki67
32
low-grade serous mutations
BRAF | KRAS
33
endometrioid carcinoma immunoprofile
``` ER+ Pax8+ Vimentin+ WT1- p53- ```
34
clear cell immunoprofile
HNF beta+ WT1- ER-
35
clear cell mutations
KRAS PTEN PIK3CA
36
mucinous immunoprofile
``` CK20+ cdx+ CK7+ ER- WT1- ```
37
mucinous mutations
KRAS
38
peritoneal carcinomatosis
distinctive diffuse seeding of peritoneum small shallow implants cytology of ascites can aid Dx
39
what can be used to follow course of surface epi tumors?
CA-125
40
High albumin gradient
``` cirrhoiss alcoholic hepatitis heart failure/constrictive pericarditis massive hepatic mets budd-chiari syndrome portal v thrombosis idiopathic portal fibrosis ```
41
low albumin graident
``` peritoneal carcinomatosis peritoneal TB pancreatits serositis nephrotic syndrome ```
42
granulosa-thecal cell tumors
``` any age 2/3 in postmenopausal eomen hormonally active 75% produce E yellow inhibin + FOXL2 mutation callexner bodies can cause vaginal bleeding ```
43
fibromas
``` very common solid white hard fibrous tumor usually u/l bening associated with meig syndrome ```
44
meig syndrome
ascites pleural effusion ovarian fibroma resolves with resection of fibroma
45
sertoli-leydig cell tumors
rare all ages 50% produce androgens
46
germ cell tumors
``` teratomas dysgerinomas endodermal sinus (yolk sac) choriocarcinomas tend to be benign in adutls and malignant inkids ```
47
dermoids
benign cystic teratoma 2-3 germ cell lines distinctive rokitanski nodule 1% develop CA (usually SCC)
48
immature malignant tertatoma
girls and adolescents contain immature tissues (embryonal and fetal) rapid growth and spread
49
monodermal (specialized teratomas)
single tissue predominates carcinoids or struma ovarii most common functional -> hyperthyrodism and carcinoid syndrome
50
dysgerminoma
``` ALL MALIGNANT ovarian counterpart to seminoma highly sensitive to radiation only 1/3 aggressive fried egg appearance on histo ```
51
endodermal sinus tumor
``` yolk sac very aggressive produces alpha fetoprotein and alpha 1 antitrypsin schiller-duval bodies kids/young adults chemo ```
52
choriocarcinoma
``` usually w/in another germ cell tumor psudoplacental tissue aggressive produce beta-HCG high levels no sensitive to methotrexate ```
53
krukenburg tumor
b/l mets of mucin producing signet CA cells, especially gastric origin