Path - Ovary Flashcards

1
Q

what is autoimmune oophoritis and what is almost always associated with? what can it lead to?

A

failed self tolerance of endocrine organ - ovary (histo shows CD4 and CD8 T cell and plasma cell infiltration)
Addison’s disease
infertility

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2
Q

presentation of polycystic ovary syndrome

what is a key lab finding? what are the outcomes of this?

A

obesity, hirsutism, type II DM, premature atherosclerosis, infertility (obviously)
increased LH:FSH - increased LH induces excess androgen production –> hirsutism and androgen converted to estrone –> increased risk of endometrial carcinoma

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3
Q

benign vs borderline vs malignant serous/mucinous ovarian surface epithelial tumors

A

benign: simple flat lining in PREmenopausal women (30-40)
borderline: better prognosis than malignant, but still carry metastatic potential
malignant: thick shaggy lining, most common in POSTmenopausal women (60-70)

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4
Q

genetics associated with increased risk of malignant surface epithelial ovarian tumors

A

BRCA1 have increased risk of serous carcinoma

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5
Q

type I vs type II pathways of epithelial tumors

A

I - progress from benign tumors to borderline to low grade malignant
II - arise from INCLUSION CYSTS/serous intraepithelial carcinoma and are usually high grade serous carcinomas

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6
Q

how to definitively differentiate/diagnose malignant from benign epithelial tumors?

A

destructive stromal invasion

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7
Q

what mutation is commonly associated with mucinous epithelial tumors?

A

KRAS

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8
Q

what are Brenner tumors? what is the typical presentation? gross appearance?

A

surface epithelial ovarian tumors composed of bladder like epithelium (transitional cells)
90% unilateral
solid tan/yellow and firm

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9
Q

benign vs malignant epithelial tumor clinical features

A

all present with lower ab pain and ab enlargement, urinary frequency, dysuria pelvic pressure
malignant lesions can have progressive weakness, cachexia and weight loss, massive ascites, OMENTAL CAKE (from local spread to peritoneum)

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10
Q

who usually get germ cell tumors?

A

children and young adults (15-30)

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11
Q

what is a cystic teratoma? what makes it malignant?

A

tumor composed of fetal tissue derived from two or three embryologic layers
presence of IMMATURE tissue (primitive NEUROEPITHELIUM) or somatic malignancy in the tissue (SCC of skin)

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12
Q

gross appearance of mature vs immature teratoma

A

mature: hair and sticky sebaceous debris, teeth common (looks greenish)
immature: fleshy grey tan color with lots of hemorrhaging

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13
Q

what is the most common benign germ cell tumor vs malignant?

A
cystic teratoma (most common overall)
dysgerminoma is most common malignant
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14
Q

genetic mutation associated with dysgerminoma, gross appearance, prognosis, possible lab elevation

A

express KIT and 1/3 have activating mutation in KIT gene
looks yellow/white to pinkish - soft and fleshy
96% cure rate if confined to ovary, 80% if spread
serum LDH may be elevated

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15
Q

endodermal sinus tumor presentation, key lab, gross appearance, key histological finding

A

malignant, most common germ cell tumor in CHILDREN
serum a-fetoprotein is elevated
similar to immature teratoma - very bloody
Schiller-duval bodies - central vessel surrounded by epithelium in a space lined by epithelium (GLOMERULUS-LIKE)

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16
Q

ovarian choriocarcinoma

A

composed of cytotrophoblasts and syncytiotrophoblasts (placental tissue) but NO villi
small and hemorrhagic - EARLY hematogenous spread
labs show high B-hCG (produced by syncytiotrophoblasts)
CHEMORESISTANT (placental version is responsive)

17
Q

presentation of granulosa sex cord stromal tumors, key histological finding

A

often produces estrogen - presents with signs of estrogen excess (precocious puberty if young, menorrhagia, endometrial hyperplasia if postmenopausal)
Call-Exner bodies - gland like structures with central acidophilic material

18
Q

what biomarker is used to monitor treatment in granulosa tumors? what mutation is present in adults but not juveniles?

A

inhibin

FOXL2

19
Q

what are fibromas (sex cord stromal tumors) associated with in terms of clinical presentation?

A

pleural effusions, ascites = Meigs syndrome

also associated with basal cell nevus syndrome (Children)

20
Q

Sertoli-Leydig cell tumors

A

hormonally active - can produce masculinization/defeminization
over 50% have DICER1 mutation - dysregulation of micro-RNAs
histology shows REINKE CRYSTALS (pink cells with crystals)

21
Q

what does a pure Leydig cell tumor look like?

A

egg - yellow

22
Q

Krukenberg tumor

A

metastatic mucinous tumor that involves both ovaries (BILATERAL)
signet ring carcinoma (gastric origin)

23
Q

what would a mucinous tumor of the appendix with metastasis to the ovary present with?

A

pseudomyxoma peritonei - massive amounts of mucus in peritoneum