prognosis Flashcards

1
Q

HSV

A

high mortality rt

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2
Q

lichen sclerosis leukoplakia

A

incr risk SCC of vulva

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3
Q

VIN (vulvar intraepithelial neoplasia)

A
  • spont regression

- progresses to invasive carcinoma in females > 45 yrs or immunocompromised. (basaloid and warty)

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4
Q

keratinizing scc of vulva

A

prognosis related to tumor size, depth of invasion and involvement of lymph vessels.

 Lesions < 2cm = 90% 5 yr survival after tx with vulvectomy + ladectomy.
 Larger lesions w involved LNs have worse prognosis

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5
Q

DES-related vaginal adenosis

A

can lead to clear cell carcinoma of vagina

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6
Q

extramammary paget dis

A

o May remain intraepidermal for yrs and not invade or metastasize.
o Invasion = poor prognosis.

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7
Q

Embryonal Rhabdomyosarcoma (sarcoma bortyoides)

A

-invade locally –> death via penetratio peritoneal cavity or obs urinary tract

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8
Q

neuroendocrine carcinoma of cervix

A

poor

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9
Q

carcinoma of cervix

A

oPts tend to die from consequences of local tumor invasion (ureteral obstruction, pyelonephritis, uremia).
o100% 5 yr survival for microinvasive carcinomas.
o< 50% 5 yr survival for tumors extending beyond the pelvis.
–50% are detected in females w/o regular screenings.

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10
Q

endometriosis with PTEN ARID1A

A

increased risk of ovarian and endometrioid and clear cell types

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11
Q

endometrial polyps

A

rarely give rise to adenocarcinoma, can be malig

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12
Q

nonatypical endomeriod hyperplasia

A
  • if estrogen withdrawn –>cystic atrophy

- rarely progress to aenocarcinoma

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13
Q

-Type 2 endometrial serous carcinoma

A
  • if bleeding, good bc usu catch early
  • Propensity for extrauterine spread.
  • 18-27% 5 yr survival even if confined to the uterus, 80% recurrence.
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14
Q

Types 1 and 2 endometrial carcinoma

A

-based on depth/stage at prsentaiton
-Stage I (grade 1 or 2): 90% 5 yr survival.
•–Tx w surgery +/- irradiation.
-Stage I (grade 3): 75% 5 yr survival.
-Stage II or III: < 50% 5 yr survival

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15
Q

Malignant Mixed Mullerian Tumors (MMMTS) (carcinosarcomas)

A

o Prognosis based on depth of invasion and stage.
o If tumor has a heterologous mesenchymal component = worse than those who do not.
o 25-30% 5 yr survival for high-stage dz.

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16
Q

Leiomyosarcoma

A

o 40% 5 yr survival.
o Anaplastic lesions: 10-15% 5 yr survival.
o Often recur after surgery

17
Q

serous tumors of ovary (mullerian epithelium)

A

 Prognosis and tx depend on pathologic classification as both low & high grade may extend to the peritoneum.
 Borderline & malignant, confined to the ovary: 100% & 70% 5 yr survival.
 Borderline & malignant, spread to the peritoneum: 90%, 25% 5 yr survival.

18
Q

mucinous tumors of ovary (mullerian epithelium)

A

 95% 5 yr survival for stage I, noninvasive.
 90% 5 yr survival for invasive malignant tumors.
 Fatal if spread beyond the ovary.

19
Q

Pseudomyxoma Peritonei

A

intestinal obstruction and death if extensive

20
Q

endometriod tumors of ovary (mullerian epithelium)

A

75% 5 yr survival (stage I).

21
Q

clear cell carcinoma of ovary (mullerian epithelium)

A

 90% 5 yr survival if confined to the ovaries.

 Poor outcome if advanced

22
Q

immature malignant teratoma of ovary

A
  • Stage I, grade 1 = excellent prognosis.
  • Prophylactic chemo if higher grade yet confined to the ovary.
  • Recurrences occur in first 2 yrs.
  • Longer absence = excellent chance of cure.
23
Q

dysgerminoma of ovary

A

 Excellent prognosis with salpingooophorectomy if seen only in the ovary.
 80% survival in those extended beyond ovary

24
Q

yolk sac tumor of ovary

A

80% survival with chemo regardless of dz stage.

25
Q

granulosa cell tumor of ovary

A

 85% 10 yr survival.

 If predominantly composed of theca cells it is unlikely to be malignant.

26
Q

gonadoblastoma

A

excellent if excised

27
Q

complete mole

A

o 2.5% risk of choriocarcinoma.

o 15% risk of persistent or invasive mole.

28
Q

partial mole

A

o ↑ risk of persistent molar dz.

o Not associated with choriocarcinoma

29
Q

choriocarcinoma

A

o Evacuation of uterine contents + chemo.
o 100% remission and high cure rate.
o Cured pts can have subsequent normal pregnancies and deliveries

30
Q

Placental Site Trophoblastic Tumor (PSTT)

A
  • Localized dz = excellent prognosis.

* Dissminated dz = 10-15% mortality.