Obstetrics
and Gynecology Board Review Practice Questions
Book 2 - 2004
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QUESTION
71.
Your patient has a microcytic anemia on her first set of prenatal
labs.
All
of the following statements are correct EXCEPT:
A)
The most commonly encountered anemia in pregnancy is Iron
Deficiency Anemia which has the following characteristics:
microcytic, hypochromic, MCV < 80 f/L, Serum Fe <
50 mcg/dL, MCHC < 30%, Serum ?Ferritin, ?TIBC
B) Combined Fe / folate deficiency is never normocytic,
normochromic anemia
C) Folate deficiency is a risk for Neural Tube Defect.
D) Most common megaloblastic anemia is folate deficiency.
E) Vitamin B12 deficiency is associated with malabsorption
diseases.
ANSWER
71. B Combined
Fe/folate deficiency is never normocytic, normochromic anemia
The
maternal blood volume rises by about one-third to provide
for the increase in uteroplacental vasculature and pregnancy
related venous dilatation. The plasma volume rises about 45%,
but the red cell volume only rises by about 25%. This causes
hemodilution producing the physiological anemia of pregnancy.
Hemoglobin level may fall, but mean corpuscular volume [MCV]
and mean corpuscular hemoglobin [MCH] both remain unchanged.
The result of combined iron and folic acid deficiency
may be a normocytic, normochromic anemia. Anemia in pregnancy
can increase the chances of fetal hypoxia, intra uterine growth
restriction, premature labor, and puerperal sepsis. Folic
acid deficiency is associated with a higher incidence of abruption.
Post partum hemorrhage is not more common, but if moderate
hemorrhage occurs, it may have profound results. When anemia
is found late in pregnancy the patient may have iron deficiency,
folic acid deficiency, hemoglobinopathy, exaggerated physiological
anemia, occult blood loss, and/or primary hypoplasia of the
bone marrow, and further evaluation should be entertained.
1.
Beischer NA, Mackay EV, Colditz PB. Obstetrics and the Newborn,
3rd edition, London: WB Saunders, 1997, chapter 36.
2.
P. Zieve & L. Waterbury, “Abn. Red Cell and Hemoglobin
Production” in A. M. Harvey, R. J. Johns, et al., The
Principles and Practice of Medicine, 20th edition, chapter
47, NY: Appleton-Century-Crofts, 1980:499 - 503.
3.
The Merck Manual, 17th ed., Whitehouse Station, NJ: Merck
Research Laboratories, 1999, p 2049-2050.

QUESTION
103.
The following statements are correct regarding Varicella-Zoster
during pregnancy EXCEPT:
A)
Varicella-Zoster immune globulin [V-ZIG] should be administered
to the newborn if the mother developed chickenpox within
5 days prior to or 2 days following delivery
B) Maternal administration of V-ZIG reduces the occurrence
of congenital varicella syndrome
C) V-ZIG can be considered to treat the pregnant women herself
to prevent the complications of chickenpox
D) All of the above
E) None of the above
ANSWER
103. B Maternal
administration of V-ZIG reduces the occurrence of congenital
varicella syndrome
Maternal
treatment with acyclovir has not been demonstrated to reduce
or prevent fetal effects of congenital varicella syndrome.
IV administration of this drug is recommended for neonates
who develop varicella within the first 2 weeks postpartum.
Oral acyclovir given within 24 hours of the rash will reduce
new lesion formation and improve constitutional symptoms in
children, adolescents, and adults. Oral acyclovir appears
safe for pregnant women; however, varicella pneumonia is treated
with IV acyclovir to reduce maternal mortality.
V-ZIG
is expensive and sometimes hard to come by in a hurry in the
quantity needed to administer to an adult. Consider doing
some lab work to evaluate mom’s immune status. Many
people are seemingly immune even though they were never vaccinated
and do not remember having the disease. Many commercial labs
can turn a stat specimen around in 24-36 hours.
1.
ACOG Practice Bulletin # 20, “Perinatal Viral and Parasitic
Infections,” Sept. 2000.

QUESTION
229.
A 47-year-old woman presents to your office complaining of
post coital spotting for the past three months. Her last pap
smear was ten years ago. Pelvic exam reveals a fungating cervical
mass, which extends one-third of the way down the vagina.
The uterus is normal size and shape. Bimanual and rectovaginal
exam reveal smooth parametria and pelvic sidewalls. Cervical
biopsy returns poorly differentiated squamous cell carcinoma.
IVP reveals right-sided hydronephrosis.
Her
FIGO state is:
A)
IIA
B) IIB
C) IIIA
D) IIIB
E) IVA
ANSWER
229. D IIIB
Cervical
cancer is one of the most common malignancies in women in
the developing world. For this reason the FIGO staging for
cervical cancer performed clinically, not surgically. The
only adjunctive tests, which can be used to stage cervical
cancer, are intravenous pyelogram, chest x-ray, barium enema,
and cytoscopy and proctoscopy.
The
following is the staging for cervical cancer:
Stage
1 - Cancer in the cervix only
-
IA - Invasion of the cervical tissues can only be seen with
a microscope. (Further classified into 1A1 and 1A2, depending
upon depth)
-
IB - Lesions wider than 7 mm or deeper than 5 mm, or that
can be seen without a microscope (Further classified for
tumors larger or smaller than 4 cm)
Stage
2 - Cancer extends beyond the cervix, but not as
far as the pelvic wall
-
2A - Extends to upper part of the vagina, but not to parametria
-
2B - Extends to the parametrial tissues (but not to the
pelvic wall).
Stage
3 - The cancer has extended beyond Stage 2, but not
beyond the pelvic area. Note: although this system does not
include lymph node sampling, in other systems a positive lymph
node would put the cancer in Stage 3.
-
3A - The cancer has spread to the lower third of the vagina,
but nowhere else.
-
3B - The cancer has spread to the pelvic wall, or has blocked
a ureter
Stage
4 - Cancer has spread to the bladder, rectum, or
outside the pelvis.
-
4A - Spread to the rectum or bladder.
-
4B - Spread (metastasis) to distant organs such as the lungs
or liver.
The
presence of hydronephrosis or pelvic sidewall involvement
classifies this patient as a FIGO Stage IIIB cervical carcinoma.
1.
Morrow CP, Curtin JP, (eds.). Gynecologic Cancer Surgery.
1st edition. Livingston NY. Churchill. 1996:469
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