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Middle East Fertility Society Journal
Middle East Fertility Society
ISSN: 1110-5690
Vol. 9, Num. 2, 2004, pp. 173-175
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Middle East Fertility Society Journal, Vol. 9, No. 2, 2004, pp. 173-175
CASE
REPORT
Heterotopic pregnancy following induction of
ovulation in PCOS
Mohamed
Addar, M.D.,
A.B.O.G.
Department
of Obstetrics and Gynecology, KingKhaledUniversityHospital, Riyadh, Saudi Arabia
Address Correspondence to: Dr. M. Addar, Associate Professor & Dept. Head,
OB/Gyn Dept. (No. 36), King Khaled University Hospital, P.O.Box. 7805, Riyadh11472,
Saudi Arabia, Tel: 966-1-967-0818, Fax: 966-1-467-1945, Email: maddar2001@hotmail.com
Received on April 18, 2004;
revised and accepted on May 3, 2004
Code Number: mf04030
ABSTRACT
A case of successful intrauterine pregnancy
diagnosed after surgical removal of a ruptured ectopic pregnancy in a patient
subjected to induction of ovulation for PCOS. Heterotopic pregnancy is a
problem with increasing incidence that needs high alertness to avoid serious
complications.
Key Words:
Ectopic pregnancy, induction of ovulation, heterotopic pregnancy
INTRODUCTION
Heterotopic pregnancy or combined intrauterine and extrauterine pregnancy
was first reported in 1708 (1). Traditionally, the rate of occurrence has been
thought to be 1:30,000 pregnancies, but in the recent literature a rate of
1:2600 has been reported in high-risk groups with the use of assisted reproduction
techniques (1), although, a rate of 1:100 has been reported with the use of
these techniques by Tal et al in 1996 (2).
This report presents a case of combined intrauterine and tubal pregnancy after
the use of ovulation induction for the treatment of infertility, with special
emphasis on the issues of diagnosis and therapeutic problems.
CASE REPORT
A 24 years old lady, known as a case of primary infertility for 5 years and
polycystic ovaries. She was overweight, and had mild hirsutism. She received
ovulation induction by Clomiphene citrate 100 mg/ day starting on day 2 of
the cycle and continued with recombinent FSH 100 I.U./day on day 7. Transvaginal
ultrasound on day 9 showed 2 follicle in the right ovary measuring 12.0 x 9.0
and 13.0 x 10.0 mm, and 4 follicles in the left ovary measuring 10.0 x 10.0,
12.0 x 13.0, 14.0 x 9.0, and 9.0 x 9.0 mm. She continued to receive the same
dose of FSH for 2 days and a repeat ultrasound on day 12 showed 2 good size
follicles in the right ovary measuring 20.0 x 18.0, and 19.0 x 23.0 mm, in-addition
to other small follicles less than 10.0 mm. The left ovary contained 2 good
size follicles measuring 22.0 x 17.0 and 25.0 x 18.0 in-addition to other small
follicles less than 10.0 mm. There was no fluid in the Pouch of Douglas and
the endometrium was 10.0 mm thick. She was given 10,000 I.U. of HCG on day
12 and was advised for natural intercourse on day 13. No Progesterone support
was added. Her next presentation to the clinic was at 5 weeks of amenorrhea
with severe lower abdominal pain and vaginal bleeding. She had a positive pregnancy
test and ultrasound scanning showed fluid collection in the Pouch of Douglas,
empty uterus and a right adnexal mass suggestive of ectopic pregnancy. She
had an emergency laparoscopy, which diagnosed a ruptured right-sided ectopic
tubal pregnancy, therefore, laparotomy was carried out and right-sided salpingectomy
was performed. Blood transfusion was not needed for the patient as her Haemoglobin
was 9.0 g/l pre-operatively and she was stable hemodynamically during surgery.
No Beta HCG sub unit was requested pre- or post- operatively
During her post-operative stay, she continued to complain of vaginal bleeding,
abdominal pain, and severe nausea. A repeat ultrasound scan was done on the
fifth post-operative day showed a small intrauterine gestational sac with a
small yolk sac but no fetal pole. Histology of the operative specimen confirmed
the presence of chorionic villi. She was given vaginal Progesterone support
post-operatively. A follow up scan was done 1 week later showed a viable intrauterine
pregnancy which was followed out till term and ended in spontaneous vaginal
delivery of a healthy baby boy.
DISCUSSION
Ectopic pregnancy is a major cause of morbidity and mortality in reproductive
age women. There is no single non-invasive test to detect the presence of an
ectopic pregnancy. The old traditional teaching that the presence of an intrauterine
pregnancy excludes an ectopic is not applicable any more in current practice.
Combined intrauterine and ectopic pregnancy is an insidious disease with a constant
increase in incidence especially in infertile women subjected to assisted reproduction
techniques with a rate of 1.5% among all IVF patients (3). The combined use of
serum beta human chorionic gonadotropin (HCG) level along with transvaginal ultrasound
improved the sensitivity to diagnose intrauterine pregnancy to 100% (4), but
for ectopic pregnancy or a combined intra and extrauterine pregnancy a high suspicion
should be present in the managing physician especially in patients submitted
to assisted reproduction in order to avoid serious maternal life threatening
conditions such as rupture of an ectopic
pregnancy.
Most of the heterotopic pregnancies present in the first trimester as in this
case report. Once a heterotopic pregnancy is diagnosed, the next dilemma that
arises is how to manage it without harming the intrauterine pregnancy. In cases
similar to our case with ruptured ectopic pregnancy, the standard treatment
is surgical removal of the ectopic either by laparoscopy or laparotomy with
minimal manipulation of the uterus. In stable patients, many other alternatives
has been reported such as ultrasound guided injection of Potassium Chloride
(4,5), local administration of Methotrexate into the ectopic pregnancy (6),
or aspiration of the ectopic sac under ultrasound guidance followed by local
injection of Methotrexate. The follow up of surviving intrauterine pregnancies
has been reported to be normal after that with a rate of successful pregnancy
and delivery of 43% (3).
The worse of all scenarios is diagnosing the ectopic pregnancy and missing
the diagnosis of the intrauterine pregnancy with the administration of parental
Methotrexate to treat the ectopic which may lead to multiple anomalies in the
developing fetus. It was recommended previously to perform D&C prior to
Methotrexate administration if the Beta HCG level is less than 2000 mIU/ml
to avoid Methotrexate embryopathy (7).
In conclusion, Knowledge of the possibility of heterotopic pregnancy and understanding
the epidemiological risk factors associated with it are important for early
diagnosis and avoiding complications. All patients who undergo assisted reproduction
should be submitted to careful monitoring in early pregnancy.
REFERENCES
- Bright DA, Gaupp FB. Heterotopic
pregnancy: A reevaluation. J Am Board Fam Pract 1990; 3 (2): 125-8.
- Tal J, Haddad S, Gordon N, Timor-Tritsch
I. Heterotopic pregnancy after ovulation induction and assisted reproduction
technologies: a literature review from 1971 to 1993. Fertil Steril 1996;
66 (1): 1-12.
- Mantzavinos T, Kanakas N, Zourlas
PA. Heterotopic pregnancies in an in-vitro fertilization program. Clin
Exp Obstet Gynecol 1996; 23 (4): 205-8.
- Barnhart KT, Katz I, Hummel A,
Gracia CR. Presumed Diagnosis of ectopic pregnancy. Obstet Gynecol 2002;
100: 505-10.
- Rizk B, Tan SL, Morcos S, Riddle
A, Brinsden P, Mason BA, Edwards RG. Heterotopic pregnancies after in vitro
fertilization and embryo transfer. Am J Obstet Gynecol 1991; 164(1 pt 1):
161-4.
- Oyawoye S, Chander B, Pavlovic
B, Hunter J, Gadir AA. Heterotopic pregnancy: Successful management with
aspiration of corneal/interstitial gestational sac and instillation of small
dose of methotrexate.
Fetal Diag Ther 2003; 18(1): 1-4.
- Stovall TG. Early pregnancy loss
and ectopic pregnancy, in Novak's Gynecology 13th ed; Jonathans. Berek;
Lippincott Williams & Wilkins, ch.17; P 528.
© Copyright 2004 - Middle East Fertility Society
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