7 |
Role-play. Woman attends for pre-pregnancy counselling as she plans
her 1st. pregnancy. |
8 |
EMQ. Hepatitis C and pregnancy. HCV |
9 |
EMQ. Medical examiner system |
10 |
EMQ. Gestational trophoblastic disease |
11 |
EMQ. Kallmann’s syndrome |
12 |
SBA. Fetal origins of adult disease |
7. Role-play. Prepregnancy counselling.
Candidate’s instructions.
You are the SpR in the gynaecology clinic. You have been asked to see
Jenny Williams, who has come for pre-pregnancy counselling.
Letter from the General Practitioner.
5 High Street,
Deersworthy,
Kent.
DO9 1JY.
Re Mrs. J. Williams,
Manor Place,
Deersworthy.
Dear Dr.,
Please see this woman who is planning pregnancy. I understand that her
sister has had a baby with Down’s syndrome. I have explained that this
increases her risk of having a similarly-affected baby to a significant degree.
Regards,
Dr. Jolly.
8. EMQ. Hepatitis C and pregnancy.
Abbreviations.
DAAD: Direct-acting,
antiviral drug.
HBV: Hepatitis B virus.
HCV: Hepatitis C virus.
HCAb: Hepatitis C antibody.
ROM: Rupture of membranes.
Scenario
1.
Which, if any, of the following
statements are true?
Option list.
A |
Hepatitis kills more people world-wide than HIV |
B |
Hepatitis kills more people world-wide than TB |
C |
Hepatitis B kills more people world-wide that
Hepatitis C |
D |
Hepatitis B kills more people world-wide than TB |
E |
None of the above |
Scenario
2.
Which, if any, of the following
statements are true in relation to HCV?
Option list.
A |
It is a DNA virus |
B |
It is a RNA virus |
C |
It is a member of the Flaviviridae family |
D |
it is a member of the Hepadnaviridae family |
E |
it is a member of the Herpesviridae family |
F |
most infections are due to genotypes 1 & 3 |
G |
most infections are due to genotypes 2 & 4 |
Scenario
3.
What is the approximate prevalence
of HCV infection in the UK?
Option list.
A |
0.1 per 1,000 |
B |
0.3 per 1,000 |
C |
0.5 per 1,000 |
D |
1 per 1,000 |
E |
3 per 1,000 |
F |
5 per 1,000 |
G |
10 per 1,000 |
H |
13 per 1,000 |
I |
15 per 1,000 |
J |
None of the above |
Scenario
4.
What are the key aspects of the
WHO’s Global Health Sector Strategy in relation to
HCV infection?
Option list.
A |
elimination as a as a major public health threat by
2020 |
B |
elimination as a as a major public health threat by 2030 |
C |
elimination as a as a major public health threat by
2040 |
D |
reduction in incidence by 50% by 2030 |
E |
reduction in incidence by 75% by 2030 |
F |
reduction in incidence by 80% by 2030 |
G |
reduction in mortality by 50% by 2030 |
H |
reduction in mortality by 65% by 2030 |
I |
reduction in mortality by 70% by 2030 |
Scenario
5.
What is the incubation period of
HCV infection?
Option list.
A |
6 weeks |
B |
2 months |
C |
up to 3 months |
D |
up to 4 months |
E |
up to 6 months |
F |
up to 12 months |
G |
none of the above |
Scenario
6.
What symptoms are most common in
acute HCV infection? There is no option list.
Scenario
7.
How is acute HCV infection
diagnosed?
Option list.
A |
clinically |
B |
presence of HCV antibody |
C |
presence of HCV RNA |
D |
none of the above |
Scenario
8.
What proportion of those with
acute HCV infection are asymptomatic?
Option list.
A |
10% |
B |
20% |
C |
50% |
D |
60% |
D |
70% |
E |
> 80% |
Scenario
9.
When does continuing infection
after initial exposure become defined as chronic
infection?
Option list.
A |
after 6 weeks |
B |
after 2 months |
C |
after 3 months |
D |
after 4 months |
E |
after 6 months |
F |
after 12 months |
G |
none of the above |
Answer. E.
After 6 months.
Scenario
10. Approximately how many of those with acute HCV infection will go on to
chronic
infection?
Option list.
A |
10% |
B |
20% |
C |
40% |
D |
50% |
E |
>50% |
F |
>70% |
Scenario
11. A woman is found to have HCV antibodies. Which, if any, of the following
statements
could be true?
Option list.
A |
she could have acute HCV infection |
B |
she could have chronic infection |
C |
she could have had HCV infection that has cleared
spontaneously |
D |
she could have had HCV infection that has responded
to drug therapy |
E |
she could have a false +ve test result |
F |
she could have chronic HBV infection due to cross
reaction with HBcAg |
G |
she is immune to HCV |
H |
the antibodies could result from HCV vaccine |
I |
the antibodies could result from yellow fever
vaccine |
J |
none of the above |
Scenario
12. Which, if any, of the following statements reflect current thinking
about the
mechanisms of damage in chronic HCV
infection?
Option list.
A |
hepatic damage is proportional to the duration of
HCV infection |
B |
hepatic damage is a direct result of HCV replication
within hepatocytes |
C |
hepatic damage is proportional to the level of
detectable HCV RNA in maternal blood |
D |
hepatic damage is immune-mediated |
E |
hepatic damage is due to progressive biliary tract
infection, scarring and stenosis |
F |
hepatic damage mostly occurs in women who abuse
alcohol |
G |
hepatic damage is worse in women with co-existing
HIV infection |
H |
hepatitis D is end-stage hepatitis C, with cirrhosis
and liver failure, ‘D’ originating from the original name: ‘deadly-stage’ HCV
disease |
Scenario
13. How common is vertical transmission? There is no option list.
Scenario
14. Which, if any, of the following statements are true in relation
to the hepatitides?.
A |
acute hepatitis is notifiable |
B |
chronic hepatitis is notifiable |
C |
hepatitis A is notifiable as the main
route of spread is faecal contamination of food & water |
D |
hepatitis D is notifiable as the main
source of infection is infected food and water |
E |
hepatitis E is notifiable as the main
source of infection in the UK is raw or undercooked pork |
F |
none of the above |
Scenario
15. What anti-viral treatment is recommended for pregnancy? There is no
option list.
Scenario
16. Which, if any, of the following are true about Ribavirin?
Option list.
A |
it is the least expensive of the new DAADs for HCV |
B |
it is the least toxic of the new DAADs for HCV |
C |
it is the most effective of the new DAADs for HCV |
D |
it is contraindicated in pregnancy because of fears
of teratogenicity |
E |
can cause sperm abnormalities |
F. |
can persist in humans for up to 6 months |
G. |
none of the above |
Scenario
17. A woman with chronic HCV wishes to breastfeed. What advice would you
give? There is no option list.
Scenario
18. How is neonatal infection diagnosed? There is no option list.
Scenario
19. How is neonatal infection treated? There is no option list.
Scenario
20. Which, if any, of the following conditions is more common in women with
HCV infection?
A |
dermatitis herpetiformis |
B |
HELLP syndrome |
C |
obstetric cholestasis |
D |
postnatal depression |
E |
thrombocytopenia |
Scenario
21. By how much is the risk of the condition in question 20 increased in
women with HCV?
Option list.
A |
by a factor of 2 |
B |
by a factor of 5 |
C |
by a factor of 20 |
D |
by a factor of 50 |
E |
none of the above |
Scenario
22. Which, if any, of the following statements is
true about HCV and the Nobel Prize?
Option list.
A |
the Nobel Prize was awarded to Alter,
Houghton & Rice in 2020 |
B |
the Nobel Prize was awarded to Alter,
Hogg & Rice in 2020 |
C |
the Nobel Prize was awarded to Alter,
Houghton & Rees in 2020 |
D |
the Nobel Prize was awarded to Change,
Houghton & Rice in 2020 |
E |
the Nobel Prize was awarded to Change,
Hogg & Rice in 2020 |
F |
the Nobel Prize was awarded to Change,
Hogg & Barleycorn in 2020 |
G |
the Nobel Prize has not been awarded for
work on HCV |
9. EMQ. Medical examiner system.
Abbreviations.
MCCD: medical certificate of the cause of
death.
ME: medical examiner.
Do I really need to know this stuff? This is
‘hot’: MEs were an innovation in 2018.
Question 1.
Which, if any, of the following are included in
the role of the ME?
Option list.
A |
scrutiny
of all death certificates from the NHS Trust |
B |
scrutiny
of all death certificates from the local area |
C |
scrutiny
of non-coronial death certificates from the local area |
D |
deciding
if postmortem examination is appropriate |
E |
supervision
of postmortem examination |
F |
deciding
on and arranging further investigations to establish the cause of death |
G |
liaison
with the coroner |
H |
discussing
the cause of death with the family of the deceased |
I |
directing
police investigations in cases of suspicious death |
Question 2.
What qualifications must a ME have?
Option list.
A |
be
registered with the GMC |
B |
be
licensed to practise or be < 5 years into retirement |
C |
be
a member or fellow of a Royal Medical College |
D |
be
a member or fellow of the Royal College of Pathologists |
E |
none
of the above. |
Question 3.
Which, if any, of the following are included in
the role of the medical examiner?
Option list.
A |
discussing
the case with the doctor who provided care during the final illness |
B |
reviewing
the medical records |
C |
deciding
the cause of death to be put on the certificate of death |
D |
discussing
the cause of death with next of kin |
E |
identifying
any concerns the next of kin may have about the care |
F |
providing
medical advice to the coroner |
G |
identifying
deaths that should trigger a mortality case record review |
Question 4.
Which, if any, of the following are included in
the role of the National ME?
Option list.
A |
being
a member of the medical team responsible for the Queen’s health |
B |
appointing
Trust MEs |
C |
disciplining
errant MEs |
D |
producing
reports |
E |
arbitrating
in disputes between MEs and coroners about the cause of death |
F |
dealing
with appeals by families who are dissatisfied with the MCCD or the care |
10. EMQ. Gestational trophoblastic disease.
Abbreviations.
CHM: complete
hydatidiform mole.
EPT: epithelioid
tumour.
GI: gastro-intestinal.
GTD: gestational
trophoblastic disease.
GTDTC: gestational
trophoblastic disease treatment centre.
GTN: Gestational
trophoblastic neoplasia.
HM: hydatidiform
mole.
PHM: partial
hydatidiform mole.
POC: products
of conception.
PSTT: placental
site trophoblastic tumour.
Option list.
A |
100%. |
B |
20%. |
C |
15%. |
D |
10%. |
E |
5%. |
F |
2.5%. |
G |
1.5%. |
H |
0.5%. |
I |
1 in 35. |
J |
1 in 55. |
K |
1 in 65. |
L |
1 in 700. |
M |
1 in 1,000. |
N |
Ö64. |
O |
pr2. |
P |
increased. |
Q |
reduced. |
R |
increased by a factor of 2. |
S |
increased by a factor of 5. |
T |
increased by a factor of 10. |
U |
increased by a factor of 20. |
V |
increased by a factor of 30. |
W |
increased by a factor of > 100. |
X |
hydatidiform mole, both partial and complete. |
Y |
hydatidiform mole, both partial and complete and
placental site tumour. |
Z |
partial mole, complete mole, invasive and metastatic
mole, choriocarcinoma, placental site trophoblastic tumour and epithelioid
trophoblastic tumour. |
AA |
choriocarcinoma invasive and metastatic mole and
epithelioid trophoblastic tumour. |
BB |
true |
|
false |
|
none of the above. |
Scenario 1.
List the
conditions included in the term GTD. There is no option list, just make a list.
Scenario 2.
What is the difference between GTD and GTN?
Pick one option from the list below.
Option list.
A |
GTD comprises the non-malignant conditions, i.e.
complete and partial moles. GTN comprises the malignant conditions: invasive mole,
choriocarcinoma and PSTT |
B |
GTD comprises all the trophoblastic conditions; GTN
comprises the malignant conditions |
C |
GTD comprises all the trophoblastic conditions; GTN comprises
persistent GTD |
D |
GTD comprises all the trophoblastic conditions; GTN comprises
malignant and potentially malignant conditions, including atypical placental
site nodules |
E |
none of the above |
Scenario 3.
GTG38 mentions one
thing as the minimum standard of care. What is it?
There is not option list as
that would make it too easy.
Scenario 4.
What is the
incidence of GTD in the UK?
Scenario 5.
Which , if any, of
the following are true of complete moles?
A |
are usually diploid and with all
the chromosomal material of paternal origin |
B |
are usually triploid, with 2
sets of paternal haploid genes + 1 set of maternal haploid genes |
C |
are usually triploid, with 1
set of paternal haploid genes + 2 sets of maternal haploid genes |
D |
are tetraploid or mosaics in
up to 10% of cases |
E |
up to 80% are due to
duplication of a single sperm in an egg devoid of maternal chromosomes |
F |
up to 80% are due to
duplication of a single sperm in a normal egg |
G |
usually result from dispermic
fertilisation of a normal egg |
H |
usually result from dispermic
fertilisation of an egg devoid of maternal chromosomes |
I |
usually has 46XX makeup |
J |
usually has 46XY makeup |
K |
the presence of fetal red
blood cells defines a mole as partial |
L |
mitochondrial DNA is maternal |
M |
mitochondrial DNA is paternal |
Scenario 6.
Which, if any, of
the following are true of partial moles?
Option list.
A |
are usually diploid and with
paternal chromosomal material |
B |
are usually triploid, with 2
sets of paternal haploid genes + 1 set of maternal haploid genes |
C |
are usually triploid, with 1
set of paternal haploid genes + 2 sets of maternal haploid genes |
D |
are tetraploid or mosaics in
up to 10% of cases |
E |
up to 80% are due to
duplication of a single sperm in an egg devoid of maternal chromosomes |
F |
up to 80% are due to
duplication of a single sperm in a normal egg |
G |
usually result from dispermic
fertilisation of a normal egg |
H |
usually result from dispermic
fertilisation of an egg devoid of maternal chromosomes |
I |
usually has 46XX makeup |
J |
usually has 46XY makeup |
K |
the presence of fetal red
blood cells defines a mole as partial |
L |
mitochondrial DNA is maternal |
M |
mitochondrial DNA is paternal |
Scenario 7.
What is the ratio
of complete: partial moles?
Scenario 8.
What is the risk
of molar pregnancy at age < 15 compared to age 30?
Scenario
9.
What is the risk
of molar pregnancy at age > 45 compared to age 30?
Scenario 10.
What is the risk
of molar pregnancy in a pregnancy after a complete mole?
Option list.
A |
< 1% |
B |
1-2% |
C |
3-5% |
D |
6-10% |
E |
11-20% |
F |
> 20% |
Scenario 11.
What is the risk
of molar pregnancy in a pregnancy after a partial mole?
Use the option list from the
previous question.
Scenario 12.
Which, if any, of
the following are more common in pregnancy after a molar
pregnancy? This is not a true
EMQ as there may be > 1 correct answer.
Option list.
A |
anaemia |
B |
eclampsia / severe PET |
C |
intrauterine growth
retardation |
D |
miscarriage |
E |
premature labour |
F |
PPH |
G |
pulmonary embolism |
G |
none of the above |
Scenario 13.
Which, if any, of
the following statements about hCG are true?
A |
is a glycoprotein |
B |
shares its α sub-unit with
FSH, LH & TSH |
C |
shares its α sub-unit with
FSH & LH but not TSH |
D |
shares its β sub-unit with
FSH, LH & TSH |
E |
shares its β sub-unit with
FSH & LH but not TSH |
F |
β-core exists as a sub-type
of β-hCG |
G |
nicked free-β exists as a
sub-type of β-hCG |
H |
c-terminal peptide exists as
a sub-type of β-hCG |
I |
hCG β core fragment may lead
to false –ve results with urine pregnancy tests |
J |
heterophile antibodies may
give false +ve hCG results |
K |
heterophile antibodies are
not found in urine |
pregnancy ?
A |
definite diagnosis is usually made by ultrasound |
B |
definitive diagnosis requires a +ve test for P57KIP2
|
C |
definitive diagnosis requires an hCG level > twice the
median value for gestation |
D |
definite diagnosis requires histological examination |
E |
none of the above |
Scenario 15.
Cystic placental spaces in the placenta and
a ratio of transverse to anterioposterior
measurements of the gestation sac <1.5 are strongly
suggestive of a partial mole. True / False.
Scenario 16.
When should invasive karyotype testing be
considered?
A |
twin pregnancy with complete
mole and a normal twin |
B |
uncertainty whether this is a
complete mole with a normal twin or possible partial mole |
C |
partial molar pregnancy |
D |
suspected mesenchymal
hyperplasia of the placenta |
E |
recurrent molar pregnancy |
F |
none of the above |
Scenario
17. Which, if any, of the following statements are true about
twin pregnancy with a viable
pregnancy and a CHM?
A |
the woman should be referred to a feto-maternal
specialist |
B |
the woman should be referred to a GTDTC |
C |
fetal karyotyping should be done |
D |
the rate of early fetal loss is about 20% |
E |
the rate of preterm birth is about 40% |
F |
the rate of preeclampsia is 20% |
G |
the incidence of GTN in doubled if the pregnancy goes
beyond 24 weeks |
Scenario
18. Which, if any, of the following statements are true about
preparation of the cervix
before evacuation of molar pregnancy?
A |
medical preparation is of proven efficacy in making
suction evacuation easier |
B |
medical preparation with prostaglandins ↑ trophoblastic embolisation |
C |
medical preparation with
prostaglandins ↑ the risk of needing chemotherapy |
D |
GTG 38 recommends the use of laminaria tents |
E |
none of the above |
Scenario
19. Which, if any, of the following statements are true about
evacuation of molar
pregnancies?
A |
medical management is recommended for both CMs and PMs to
↓ the risk
of bleeding |
B |
medical management is recommended for both CMs and PMs to
↓ the risk
of dissemination of trophoblastic tissue |
C |
medical management is recommended for both CMs and PMs to
↓ the risk
of uterine perforation |
D |
suction evacuation is recommended for both CMs and PMs |
E |
suction evacuation is recommended for CMs |
F |
suction evacuation is recommended for PMs so long as
fetal parts are not too big |
G |
mifepristone + misoprostol treatment is an acceptable
alternative to suction evacuation. |
H |
oxytocin administration after suction evacuation is
recommended to ↓ bleeding |
I |
none of the above |
Scenario 20.
What is the
management of suspected molar ectopic pregnancy?
A |
usual management for ectopic
pregnancy |
B |
usual management + any tissue
obtained sent to GTDTC |
C |
methotrexate followed by
usual surgical management |
D |
referral to GTDTC |
E |
none of the above. |
Scenario 21.
What is the
management of placental site trophoblastic tumour?
A |
referral to GTDTC |
B |
referral to GTDTC,
methotrexate and any tissue sent to GTDTC |
C |
referral to GTDTC,
hysterectomy and tissue sent to GTDTC |
D |
referral to and management by
GTDTC |
E |
none of the above. |
Scenario 22.
What is the
management of epitheliod trophoblastic tumour?
Use
the option list from Scenario 21.
Scenario 23.
What is the
management of placental site nodule?
Use the
option list from Scenario 21.
Scenario
24. What is the management of atypical placental site
nodule?
Use
the option list from Scenario 21.
Scenario 25.
Which, if any, of
the following statements are true about urinary hCG testing in
relation to avoiding failure to
diagnose molar pregnancy?
A |
testing should be done 3
weeks after medical evacuation of complete moles |
B |
testing should be done 3
weeks after surgical evacuation of complete moles |
C |
testing should be done 3
weeks after medical evacuation of partial moles |
D |
testing should be done 3
weeks after surgical evacuation of complete moles |
E |
testing should be done 3
weeks after medical evacuation of ‘failed’ pregnancy |
F |
testing should be done 3
weeks after surgical evacuation of ‘failed’ pregnancy |
G |
testing should be done 3
weeks after medical evacuation of ‘failed’ pregnancy, but only if POC have
not been sent for histological examination |
H |
testing should be done 3
weeks after surgical evacuation of ‘failed’ pregnancy, but only if POC have
not been sent for histological examination |
I |
testing should be done 3
weeks after medical evacuation of incomplete miscarriage |
J |
testing should be done 3
weeks after surgical evacuation of incomplete miscarriage |
K |
testing should be done 3
weeks after medical evacuation of incomplete miscarriage, but only if POC
have not been sent for histological examination |
L |
testing should be done 3
weeks after surgical evacuation of incomplete miscarriage, but only if POC
have not been sent for histological examination |
M |
none of the above |
Scenario 26.
Which, if any, of
the following statements are true in relation to histological
examination of POC after TOP?
A |
it should be done in all
cases to exclude GTD |
B |
it should be done in all
cases that have not had pre-op ultrasound examination in case the pregnancy
was an unsuspected ectopic. Absence of trophoblastic tissue on histology will
raise suspicion of the diagnosis |
C |
it should be done in all
cases where ultrasound has not shown a viable pregnancy |
D |
it should be done in all
cases where ultrasound has not shown fetal parts. |
E |
none of the above |
Scenario 27.
Which, if any, of
the following statements are true in relation to RhD and GTD?
A |
CHMs have no RhD |
B |
PHMs have no RhD |
C |
Anti-D should be withheld
until histological results are available |
D |
‘C’ is true, but only in
relation to CMs |
E |
‘C’ is true, but only in
relation to PMs |
F |
none of the above |
Scenario 28.
Which, if any, of
the following statements are true in relation to GTN?
A |
always arises from molar
pregnancy |
B |
may occur after normal
pregnancy and livebirth |
C |
may arise as primary ovarian
neoplasia |
D |
the incidence after complete
molar pregnancy is greater than after partial molar pregnancy |
E |
the incidence after livebirth
is estimated at 1 in 50,000 |
Scenario 29.
Which, if any, of
the following statements are true in relation to p57KIP2?
A |
it is a tumour suppressor
gene, found in complete and partial moles but not choriocarcinoma |
B |
takes us to the world of
genomic imprinting |
C |
is an example of uniparental
disomy |
D |
is a gene found in
chromosomes of maternal origin, but not paternal |
E |
is a gene found in
chromosomes of paternal origin, but not maternal |
F |
can help to distinguish
complete and partial moles |
G |
none of the above |
Scenario 30.
What is the risk of persistent GTD after a
complete mole?
Scenario 31.
What is the risk of requiring chemotherapy
after a complete mole?
Scenario 32.
What is the risk
of persistent GTD after a partial mole?
Scenario 33.
What is the risk
of requiring chemotherapy after a partial mole?
Scenario 34.
What is the risk
of requiring chemotherapy with hCG level > 20,000 i.u. 4+1 weeks
after
evacuation?
Scenario 35.
What is the
overall risk of requiring chemotherapy after molar pregnancy in the UK?
Scenario 36.
What is the risk
of requiring chemotherapy in the USA compared with the UK?
Scenario 37.
Which, if any, of
the following are grounds for offering chemotherapy after
hydatidiform mole?
A |
hCG > 10,000 IU/L > 4 weeks after evacuation |
B |
hCG > 20,000 IU/L > 4 weeks after evacuation |
C |
↑
hCG in two consecutive serum samples |
D |
hCG the same in two consecutive samples |
E |
raised, but falling, hCG level 3 months after evacuation |
F |
persistent bleeding 3 months after evacuation |
Scenario 38.
What are the risk
factors included in the FIGO scoring system?
Scenario 39.
Which, if any, of
the following statements is true about the recommended treatment
of low-risk GTN?
A |
low risk is defined as WHO score
≤ 5 |
B |
low risk is defined as WHO score
≤ 6 |
C |
low risk means that no treatment
is necessary |
D |
treatment of low risk GTN is
methotrexate |
E |
treatment of low risk GTN is
folic acid |
F |
treatment of low risk GTN is
folinic acid |
Scenario 40.
Which, if any, of
the following is the most common side-effect of methotrexate?
A |
alopecia |
B |
anaemia |
C |
aphasia |
D |
nausea |
E |
myelosuppression |
F |
none of the above. |
Scenario 41.
Which, if any, of
the following statements are true about the use of folic acid / folinic
acid in methotrexate treatment regimens? There
may be > 1 correct answer.
A |
folic acid must be converted to
tetrahydrofolate to be biologically active |
B |
folic acid must be converted to
folinic acid to be biologically active |
C |
dihydrofolate reductase converts
folic acid to folinic acid |
D |
dihydrofolate reductase converts
folic acid to tetrahydrofolate |
E |
dihydrofolate reductase converts
folinic acid to tetrahydrofolate |
F |
folinic acid is used in
preference to folic acid as it reaches higher levels in plasma |
G |
folate therapy is used to reduce
GI tract damage from methotrexate |
H |
folate therapy is used to reduce
hepatic damage from methotrexate |
I |
folate therapy is used to reduce
neurological damage from methotrexate |
J |
folate therapy is used to reduce
renal damage from methotrexate |
K |
none of the above. |
Scenario 42.
When
is repeat surgical evacuation of the uterus appropriate?
Scenario
43. Which, if any, of the following statements are true about
the recommended duration
of follow-up after GTD? This is not a true EMQ as there may
be > 1 correct answer.
A |
6 months from the time the hCG falls to normal |
B |
6 months from the date of evacuation of the GTD if the
hCG falls to normal within 56 days |
C |
6 months from the date of the hCG falling to normal if it
does so within 56 days |
D |
6 months from the date of evacuation of the GTD if the
hCG falls to normal after 56 days |
E |
6 months from the date of the hCG falling to normal if it
does so after 56 days |
F |
56 days after the first full moon after the evacuation of
the GTD |
Scenario 44.
What is the
approximate cure rate for GTN with a FIGO risk score ≤ 6?
A |
70% |
B |
80% |
C |
90% |
D |
95% |
E |
98% |
F |
100% |
Scenario 45.
What is the
approximate cure rate for GTN with a FIGO risk score >7?
A |
70% |
B |
80% |
C |
90% |
D |
95% |
E |
98% |
F |
100% |
Scenario 46.
When should the possibility
of persistent GTD be investigated after non-molar
pregnancy?
A |
if there is abnormal bleeding |
B |
if there is persistent abnormal
bleeding |
C |
if there is cough |
D |
if there is new-onset dyspnoea |
E |
if there is pleurodynia |
Scenario 47.
A woman wishes to become
pregnant after a pregnancy with GTD. Which, if any, of
the following statements are
true about the advice she should be given about an appropriate inter-pregnancy
interval?
A |
not before follow-up is complete |
B |
not for at least 3/12 after
completion of follow-up |
C |
not for at least 6/12 after
completion of follow-up |
D |
not for at least 12/12 after
completion of follow-up |
E |
she should be advised not to
become pregnant if chemotherapy was needed |
F |
not for at least 6 months after
completion of follow-up if chemotherapy was needed |
G |
none of the above |
Scenario 48.
Which of the
following statements are true about combined hormonal contraception
use after GTD?
A |
it may increase the risk of GTN
if used before hCG levels have returned to normal |
B |
is not associated with
additional risk |
C |
intra-uterine contraceptives are
preferable |
Scenario 49.
Which, if any, of
the following statements are true about the long-term issues for
women who have needed
chemotherapy for GTN?
A |
the menopause is likely to be
earlier |
B |
the risk of other cancers is not
increased |
C |
there is evidence of ↑ risk of breast cancer |
D |
there is evidence of ↑ risk of colon cancer |
E |
there is evidence of ↑ risk of myeloid leukaemia |
F |
there is evidence of ↑ risk of melanoma |
H |
there is no evidence of addition
risk with HRT |
Scenario 50.
A woman had a complete mole in her first
pregnancy. She is pregnant for the second
time. What is the
risk of another molar pregnancy?
Scenario 51.
A woman has had two molar pregnancies. What
is the risk of molar pregnancy if she
becomes pregnant again?
Scenario 52.
A woman has had three molar pregnancies.
What is the risk of molar pregnancy if
she becomes pregnant again?
Scenario 53.
Which, if any, of the following statements
are correct in relation to recurrence of
molar pregnancy?
A |
the histological type is likely to be the same |
B |
the histological type in recurrent mole after a
complete mole is likely to be partial mole |
C |
the histological type in recurrent mole after a partial
mole is likely to be complete mole |
D |
the histological type after PSTT is likely to be
choriocarcinoma |
E |
none of the above |
Scenario 54.
A woman has a normal pregnancy after
treatment for hydatidiform mole. Which, if
any, of the following statements are true about the need
for hCG testing 6 weeks after the pregnancy?
A |
testing is optional |
B |
testing is only needed for women with persisting GTD |
C |
testing is only needed for women with persisting GTN |
D |
testing is only needed for women who have needed
chemotherapy |
E |
testing should be offered to all women who use hair dye |
Scenario 55.
What proportion of women remain fertile
after treatment for GTN?
A |
80% |
B |
70% |
C |
60% |
D |
50% |
E |
40% |
Scenario 56.
What proportion of women will reach the
menopause by age 40 after chemotherapy
for GTN?
A |
10% |
B |
20% |
C |
30% |
D |
40% |
E |
50% |
FSRHCAP has a SBA. It is open access, so reproduced here. It is
badly-worded, mistaking GTD for GTN, but highlights some of the key points.
With gestational trophoblastic disease (GTD), which statement is
false?
A. After complete hydatidiform mole, 15–20%
women develop GTD needing chemotherapy
B. After partial hydatidiform mole, 30–35%
women develop GTD needing chemotherapy
C. Intrauterine contraception is unsuitable
while human chorionic gonadotropin is still detectable
D.
Combined hormonal contraception can be used if gestational trophoblastic
neoplasia develops
Answer. GTG38 says the risk of GTN requiring chemotherapy is
about 13–16% for CHM and 0.5–1.0% for PHM, so both A & B are false, but B
more so than A.
11. EMQ. Kallmann’s syndrome.
Abbreviations.
Ks: Kallmann’s syndrome
Scenario
23. Which of the
following might be included in descriptions of Kallmann’s syndrome?
Option list.
A |
hypogonadotrophic
hypogonadism |
B |
hypogonadotrophic
hypogonadism + anosmia |
C |
hypogonadotrophic
hypogonadism + anosmia + colour-blindness. |
D |
hypogonadotrophic
hypogonadism due to uterine agenesis |
Scenario
24. Which, if any, of
the following are features of the Kallmann phenotype?
A |
absent
or minimal breast development |
B |
aortic
stenosis |
C |
blue
eyes |
D |
blue
hair |
E |
hot
flushes |
F |
short
stature |
G |
tall
stature |
H |
vaginal
agenesis |
I |
none
of the above |
Scenario
25. How common is Kallmann’s syndrome and what is the female:
male ratio?
A |
1
in 1,000 and F:M ratio 1:1 |
B |
1
in 5,000 and F:M ratio 1:1 |
C |
1
in 10,000 and F:M ratio 1:4 |
D |
1
in 50,000 and F:M ratio 1:4 |
E |
1
in 100,000 and F:M ratio 1:8 |
F |
1
in 250,000 and F:M ration 1:10 |
Scenario
26. What is the most
common mode of inheritance of Ks?
Option list.
A |
hypogonadotrophic
hypogonadism |
B |
hypogonadotrophic
hypogonadism + anosmia |
C |
hypogonadotrophic
hypogonadism due to uterine agenesis |
D |
autosomal
dominant |
E |
autosomal
recessive |
F |
X-linked
recessive |
G |
new
mutation of the ANOS1 gene |
H |
the
most common mode of inheritance is not known |
Scenario
27. How is Kallmann’s
syndrome diagnosed?
A |
abdominal and pelvic ultrasound scan |
B |
cell-free fetal DNA |
C |
chromosome analysis |
D |
CT scan of hypothalamus / pituitary |
E |
MR scan of hypothalamus / pituitary |
F |
none of the above. |
Scenario
28. How is Kallmann’s
syndrome treated initially?
Which of the following statements are true?
Option list.
A |
GnRH analogue depot |
B |
pulsatile GnRH therapy |
C |
combined oral contraceptive |
D |
counselling & education re gender re-assignment |
E |
depot progestogen |
F |
none of the above |
Scenario
29. A woman was
diagnosed with Kallmann’s syndrome at 16 and had successful initial
treatment. She is now 25, married and wishes to have a pregnancy. She
has had pre-pregnancy assessment and counselling. Which of the following should
be considered?
A |
GnRH analogue depot |
B |
induction of ovulation with clomiphene |
C |
gonadotrophin therapy |
D |
pulsatile GnRH therapy |
E |
none of the above |
12. SBA. Fetal origins of adult disease.
Abbreviations.
ADHD: attention-deficit, hyperactivity disorder
Lead in. These questions
relate to disease in adults resulting from events during fetal, infant and
child development.
Scenario 1. What eponymous
title is given to the concept that adverse intra-uterine conditions
predispose to the
development of disease in adulthood?
Option
List
A |
the
Barker hypothesis |
B |
the
Baker’s dozen |
C |
the
Broadbank theory |
D |
PIPAD:
Placental Insufficiency Programmes Adult Disease |
E |
SIMCARD:
Stop In-utero Malnutrition to Conquer Adult-resulting Disease |
Scenario 2. Which other term
is used for the concept that adverse intra-uterine conditions
predispose to the development of disease in
adulthood?
Option
List
A |
FDAD:
fetal determination of adult disease |
B |
FIAD: fetal influences on adult disease |
C |
FIDAD:
fetal and infancy determinants of adult disease |
D |
FIGO: fetal influences on genomic outcomes |
E |
FP: fetal programming |
Scenario 3. Which of the
following is thought to increase the risk of adult disease?
Option List
A |
low
birthweight (LBW) |
B |
LBW followed by poor weight gain in infancy
and childhood |
C |
LBW
followed by poor weight gain in infancy but above-average weight gain in
childhood |
D |
above-average
birthweight (AABW) |
E |
AABW
followed by poor weight gain in infancy but above-average weight gain in
childhood |
F |
AABW
followed by above-average weight gain in infancy and childhood |
Scenario 4. Which adult
diseases are generally believed to be more likely in relation to adverse
influences on the
fetus, infant and child.
Diseases.
A |
asthma |
B |
chronic bronchitis |
C |
coronary heart disease |
D |
diabetes type I |
E |
diabetes type 2 |
F |
hypertension |
G |
Mendelson’s syndrome |
H |
Stroke |
Scenario 5. What adult
condition has been linked to raised maternal c-reactive protein levels?
Option
List
A |
asthma |
B |
ADHD |
C |
autism |
D |
inflammatory
bowel disease |
E |
schizophrenia |
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