Ovarian Pathology Flashcards

1
Q

Luteal Cyst

A
  • > 3cm
  • reproductive age
  • thick hemorrhagic fluid
  • hormone producing
  • interspersed peripheral theca cells
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2
Q

Follicular cyst

A
  • Prepubescent and reproductive age
  • Contain serosanguinous fluid
  • Thin smooth lining of inner granular and outer theca cells
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3
Q

Presence of “ectopic” endometrial tissue at a site
outside of the uterus
• Repeated cyclical hemorrhage during menstrual cycle- “chocolate” color
• Consist of normal looking endometrial glands + stroma + RBC + hemosiderin
• Induce fibrosis, adhesions, pain
• May extend along pelvic ligaments
• Usually associated with infertility

A

Chocolate cyst

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4
Q

Polycystic Ovarian Syndrome Pathogenesis

A

Caused by genetics, sedentary lifestyle, obesity
Insulin resistance—> hyperinsulinemia—> increased androgens (prolonged high estrogen levels)—> no LH surge; no ovulation—> no corpus luteum; low progesterone—> unopposed excess estrogen —> inhibits FSH—> increased LH:FSH ratio

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5
Q

Symptoms of PCOS

A

Hirsutism, acne, infertility and endometrial hyperplasia

Menstrual irregularities

Polycystic ovaries (string of pearls)

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6
Q

Cysts lined by granulosa cells and hypertrophied theca interna cells

A

PCOS

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7
Q

Type I epithelial ovarian tumors

A

progress from benign tumors through borderline tumors that may give rise to a low-grade carcinoma.
• These include low-grade serous, endometrioid, and mucinous carcinomas
• Genes involved: KRAS, BRAF

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8
Q

Type II epithelial ovarian tumors

A
  • They demonstrate high-grade features and are most commonly of serous histology.
  • STIC: Serous tubal intraepithelial carcinoma—> areas of marked epithelial atypia in fallopian tube epithelium: observed in fallopian tubes of women with germline BRCA1/2 mutations undergoing prophylactic salpingo-opherectomy
  • Genes involved: p53, Rb
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9
Q

Serous ovarian tumors
• Benign and borderline tumors
• Serous carcinomas occur later in life
• Papillae: dystrophic calcification at tips —> Psammoma bodies

What are the risk factors

A
  • Women aged 40-59 years on oral contraceptives or tubal ligation: decreased risk
  • Germline mutations in BRCA1 and BRCA2
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10
Q
A

SEROUS CYSTADENOMA

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11
Q
A

Borderline serous tumor

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12
Q
A

Serous cyst adenocarcinoma

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13
Q
  • KRAS gene mutation
  • Very large bulky masses
  • Multiloculated (M: Mucinous, M: multiloculated) tumors filled with sticky, gelatinous fluid rich in glycoproteins
  • Tall columnar cells with apical mucus vacuole, no cilia
  • Pseudomyxoma peritonei can be seen
A

Mucinous Ovarian Tumors

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14
Q

• Mucinous ascites (jelly belly)
• Cystic epithelial implants on the peritoneal surfaces, adhesions, and frequent involvement of the ovaries
• If extensive, may result in intestinal obstruction and death
• Most cases extraovarian (usually appendiceal) with secondary ovarian and
peritoneal spread

A

PSEUDOMYXOMA PERITONEI

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15
Q
  • Coexists with endometriosis & endometrial carcinoma
  • Genes involved: PTEN, microsatellite instability (MSI due to mismatch repair genes), KRAS
  • malignant
  • cystic and solid areas
  • Microscopy: presence of tubular glands resembling benign or malignant endometrium
A

ENDOMETRIOID TUMORS

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16
Q

occur in association with endometriosis or endometrioid carcinoma of the ovary + resemble clear cell carcinoma of the endometrium

Genes involved: KRAS, PTEN, p53

Microscopy: sheets of large epithelial cells with abundant clear cytoplasm

A

CLEAR CELL TUMORS

17
Q

Brenner tumors
Neoplastic epithelial cells resembling urothelium
• Gross: firm, solid and yellowish
• Microscopy: fibrous stroma (resembling that of the normal ovary) with sharply demarcated nests of epithelial cells (resembling the epithelium of the urinary tract)

A

TRANSITIONAL CELL TUMORS

18
Q

Dermoid cysts
Lined by skin
Young women
Gross: Unilocular cyst containing hair and sebaceous materials

A

Mature Teratoma (benign)

19
Q

Prepubertal and young adults (~18 yrs.)
Contain tissues that resemble embryonal and primitive fetal tissue
Gross: more solid
Micro: immature neuroepithelium, cartilage, bone, muscle, and other elements

A

Immature (malignant) teratoma

20
Q
  • Single dominant differentiation like thyroid, neuroendocrine cells etc
  • Thyroid tissue- “Struma ovarii”- hyperthyroidism
  • Neuroendocrine- “Carcinoids”- carcinoid syndrome
A

Monodermal teratoma

21
Q

Presence of Alpha-fetoprotein and alpha 1 antitrypsin

Glomerulus-like structure composed of a central blood vessel enveloped by tumor cells within a space that is also lined by tumor cells—> Schiller-Duval body (*)

In young women and children

Presenting with abdominal pain and a rapidly growing pelvic mass

A

Yolk Sac Tumor

22
Q

Malignant
• Genes involved: c-kit
• Serum tumor marker: Lactate dehydrogenase (LDH), human chorionic gonadotropin (hCG) (if syncytiotrophoblasts also present)
• Gross: unilateral, solid, fleshy, yellow-white to grey-pink, homogenous
• Microscopy: large vesicular cells in sheets with clear cytoplasm, well defined cell boundaries, and centrally placed regular nuclei; scant fibrous stroma rich in
infiltrating lymphocytes
• Very responsive to chemotherapy

A

Dysgerminoma

23
Q

Can be gestational (arising in placenta) or non gestational (arising in ovary)

Aggressive —> usually metastasized hematogenously to the lungs, liver, bone, and other sites by the time of diagnosis

High levels of chorionic gonadotropins

Generally unresponsive to chemotherapy and are often fatal

A

Choriocarcinoma

24
Q

Composed of cells that resemble granulosa cells of a developing ovarian follicle
Large amounts of estrogen
• In prepubertal patients: precocious sexual development
• In adult women: proliferative breast disease, endometrial hyperplasia, and endometrial carcinoma
• Gross: usually unilateral, hormonally active have a yellow coloration to their cut surfaces
• Microscopically: small, distinctive, glandlike structures filled with an acidophilic material recall immature follicles (Call-Exner bodies)
• Serum tumor marker: inhibin**

A

Granulosa Cell Tumors

25
Q

Arising in the ovarian stroma that are composed of either fibroblasts (fibromas) or plump spindle cells with lipid droplets (thecomas)

• Gross: usually solid, spherical, encapsulated, hard, grey-white masses covered by glistening, intact ovarian serosa
• Microscopy: composed of well-differentiated fibroblasts and scant interspersed collagenous stroma
Hormonally inactive

A

Fibroma

Two curious associations:

  1. Ovarian tumor + hydrothorax + ascites =Meigs syndrome
  2. With basal cell nevus syndrome
26
Q

masculinization or defeminization

atrophy of the breasts, amenorrhea, sterility, and loss of hair

May progress to striking virilization (hirsutism) —> male hair distribution, hypertrophy of the clitoris, and voice changes.

A

Sertoli-Leydig Cell Tumors

27
Q

Metastatic/ Secondaries

A

• Most common metastatic tumors of the ovary are derived from tumors of müllerian origin: the uterus, fallopian tube, contralateral ovary, or pelvic peritoneum
• Most common extra-müllerian tumors metastatic to the ovary: carcinomas of the breast and gastrointestinal tract, including colon, stomach, biliary tract, and pancreas.
• Also included in this group are rare cases of pseudomyxoma peritonei, derived from appendiceal tumors
• Classic metastatic gastrointestinal carcinoma involving the ovaries is termed
**Krukenberg tumor—> characterized by bilateral metastases composed of mucin producing cancer cells with a “signet-ring” appearance, most often of gastric origin