GTD Flashcards

1
Q

abnormal conceptions with excessive placental and little/no fetal development

A

hydatidiform moles

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2
Q

most common karyotype for h mole

A

46xx (androgenic diploidy, one sperm or 2 sperms)

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3
Q

most common pathogenesis for h mole

A

endoreduplication: empty ovum is fertilized by haploid sperm that endoreduplicates to make a homozygous complete mole

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4
Q

alternate pathogenesis for complete h mole

A

dispermy: empty ovum is fertilized by two haploid sperms giving to a heterozygous complete mole

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5
Q

h mole pattern on uts

A

snowstorm pattern

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6
Q

histopathologic appearance of h mole

A

severe trophoblastic proliferation cauing elevated bhcg

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7
Q

physiologic effects of elevated bhcg titer

A
  • corpus size is larger than aog
  • vaginal bleeding
  • presence of theca lutein cysts
  • presence of medical problems (preeclampsia, anemia, hyperthyroid, pulmo embolism causing rds)
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8
Q

most common pathogenesis in partial hm

A

dispermy on non-empty ovum = triploid partial mole (69xxy, 69xxx, 69xyy)

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9
Q

tvuts appearance

A

baby with many abnormalities or no baby (misdiagnosed as missed abortion)

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10
Q

histopath of phm

A

markedly cystic villi and normal sized villi
fetal components and rbc are present
less elevated bhcg

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11
Q

effects of elevated bhcg in phm

A

vaginal bleeding
corpus similar/smaller than aog
theca lutein cysts and associated medical problems

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12
Q

t/f management is different for the two h moles

A

false, management is similar

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13
Q

principles of h mole management

A

recognize and manage associated medical conditions
evacuate promptly and appropriately
identify patients at high risk for gtn
regular post-evan bhcg surveillance

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14
Q

medical complications that must be treated first

A
anemia
hyperemesis gravidarum
respiratory insufficiency
dic
preeclampsia
hyperthyroidism
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15
Q

t/f in patients with molar pregnancy, even if they present with elevated bp and proteinuria in the first trimester, then diagnose with pre-eclampsia

A

true

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16
Q

common presenting symptoms of hyperthyroidism in h mole

A

thyroid enlargement and tachycardia

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17
Q

possible evacuation methods for molar products

A

hysterectomy if family is completed

suction curettage

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18
Q

t/f medical induction can be done to evacuate molar products

A

FALSE, causes more bleeding and higher risk for gtns

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19
Q

management procedures for closed cervix, pre-evacuation

A

mechanical dilators and hegar dilators prior to curretage

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20
Q

t/f using prostaglanding and pre-evacuation oxytocin is NOT RECOMMENDED prior to evacuation

A

true

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21
Q

t/f theca lutein cysts indicate oophorectomy

A

false, don’t do anything they will regress in 8 weeks

only indication: with torsion, rupture, or necrosis

22
Q

confirmatory tests for h mole classification

A
immunostain p57kip2
cytogenetic studies (flow cytometry or karyotyping)
23
Q

risk of malignant degeneration of h mole

A

complete: 15-25%

partial 0.5-4%

24
Q

how to decrease risk for gtn

A

chemoprophylaxis with methotrexate

hcg surveillance

25
indications for chemoprophylaxis
- >40 yo - uterine size 6+ weeks larger than aog - theca lutein cyst of 6+ cm - medical complications - bhcg 100,000+ mlu/ml - recurrent h mole - h mole with normal twin fetus - poor follow up
26
contraindications for chemoprophylaxis
``` hgb <100 mg/dl or hct <0.3 wbc <3,000 or >10,000 platelet <100,000 neutrophils (ANC) <1.5 active infection abnormal renal/liver function ```
27
process of bhcg monitoring
1 week after evacuation every 2 weeks until 3 normal titers every month for 6 months no pregnancy
28
preferred contraceptive after h mole
barrier: not really progestins: very, irregular bleeding combined ocp!!
29
t/f iuds can cause heavy menstrual bleeding which can confuse the monitoring after h mole
true
30
t/f ocps suppress endogenous FSH
false, LH which has similar structure to bchg
31
when to allow pregnancy after h mole
after 6 mos of normal serum bhcg level
32
work-ups during pregnancy after h mole
perform early uts submit placenta for histopath monitor bhcg 6 weeks postpartum
33
when to refer for post molar gtn
rise in bhcg of 10%+ plateauing for bhcg values after evacuation presence of metastasis at any site
34
risk factors for gtn
major risk factor is antecedent pregnancy (h mole is associated with 50% of gtns) asians
35
history of gtn patient
previous h mole vaginal bleeding and anemia s/sx of metastasis
36
t/f you can do biopsy if you find a vaginal mass in px suspected with gtn
FALSE, DO NOT PERFORM BIOPSY IT WILL CAUSE BLEEDING
37
supporting evidence of gtn with clinical diagnosis
sonographic picture and elevated bhcg titer
38
t/f chest ct scan can detect occult metastases in the presence of normal cxr
true
39
t/f chest ct is used for monitoring and staging, not for risk score assessment
true
40
indications for brain ct
neuro s/sx | all px with pulmonary metastases having aggregate diameter of 3+ cm
41
FIGO anatomic staging
``` I = uterus II = outside uterus but in pelvis III = pulmonary metastasis IV = metastases to the other sites ```
42
t/f histopath is needed to start gtn treatment
false
43
t/f it's possible to treat gtn with chemo alone
true
44
treatments for gtn
nonmetastatic or metastatic low-risk: single agent methotrexate or actinomycin metastatic high risk: emaco regimen
45
when is consolidation therapy done
when patient reaches normal hcg titers <5
46
patient is cured of gtn when
3 consecutive normal serum bhcg levels
47
hcg monthly monitoring
``` monthly for first 6 mos every 2 mos for next 6 mos every 3 mos for 1 year evey 6 mos after lifetime monitoring ``` no pregnancy for first 2 years
48
complications for gtn
early menopause secondary malignancies (etoposide) av malformation in uterus
49
clinical presentation of pstt/ett
irregular uterine bleeding distant from preceding non-molar gestation
50
diagnosis for pstt/ett
histopath pstt: implantation type intermediate trophoblasts ett: chorionic type intermediate trophoblasts
51
management of pstt/ett
hysterectomy, resistant to chemo