Clinical Case Report

Heterotopic pregnancy: a clinical case report from rural Nigeria


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Michael A Odewale
1 MBBS, FMCGP, Senior consultant family physician

name here
Muhammed Afolabi
2 MBBS, FMCFM, Consultant family physician *


* Muhammed Afolabi


1, 2 Ladoke Akintola University Teaching Hospital, Osogbo, Osun State, Nigeria


22 September 2008 Volume 8 Issue 3


RECEIVED: 28 March 2008

REVISED: 22 August 2008

ACCEPTED: 22 September 2008


Odewale MA, Afolabi M.  Heterotopic pregnancy: a clinical case report from rural Nigeria. Rural and Remote Health 2008; 8: 979.


© Michael A Odewale, Muhammed Afolabi 2008 A licence to publish this material has been given to ARHEN,


Heterotopic pregnancy (HP) is the co-existence of intrauterine and ectopic pregnancies; it is said to be rare. We report the case of a 22 year old woman with HP after unsuccessful attempts at abortion. This report illustrates the treatment difficulties encountered in a delayed presentation, and the nature HP is assuming in rural practice. It also highlights the role of family physicians in reducing maternal mortality in resource-limited settings.

Key words: heterotopic pregnancy, Nigeria.

full article:


Naturally occurring heterotopic pregnancy is rare. It was first described by Duverney in 1708 at autopsy but now is more commonly diagnosed in life1. With the rising incidence of ectopic pregnancies due to increasing risk factors and expansion in assisted reproductive technologies in infertile couples, the chances of heterotopic pregnancies are increasing in many centers2,3. This patient is reported on to remind that heterotopic pregnancy is not as rare as may be assumed. The report also adds to the series of this presumably rare condition.

Case report

A 22 year old woman, a student of a polytechnic, was brought to our practice on 20 May 2006. The 20 bed clinic manned by two trained family physicians is located in Ejigbo, a rural settlement approximately 40 km from Osogbo, the capital city of Osun State, south west Nigeria. It has a functioning laboratory and ultrasound scan facilities. Our practice provides the only surgical services in the area and therefore attracts a high patient load.

The patient presented with 2 weeks' history of vaginal bleeding following an attempted induced abortion of a confirmed pregnancy. Her last menstrual period was 15 February 2006 making the gestational age 8 weeks. The patient had lower abdominal pain and intermittent vomiting but no change in bowel habits. There was no associated vertigo, fainting or urinary symptoms. She had taken several unknown medications in the preceding weeks with the intention of terminating the pregnancy. She later had a uterine evacuation in a private clinic. Vaginal bleeding did not stop after the procedure despite medication, hence the presentation at our practice. The patient had a history of multiple unprotected sexual intercourse and previous treatment with antibiotics for recurrent vaginal discharge, itching and lower abdominal pain.

General examination revealed a lethargic, moderately pale young woman. Her pulse was 90 beats/ min, regular but of low volume while her blood pressure (BP) was 80/50 mmHg (normal 120/80). There was suprapubic distension, with associated tenderness and guarding. Vaginal examination showed no active bleeding, a closed cervical os, and cervical excitation tenderness was positive. A clinical assessment was made of an incomplete abortion complicated by pelvic peritonitis. Her packed cell volume was 23% (normal value: 33-48%; haematocrit = 7 g/dL, normal range 10-13 g/dL); her blood group was O positive; white blood cell count was 6500/mm3 (normal range 4000-11 000/mm3) with 72% neutrophils and 28% lymphocytes. Her HIV status was negative.

The patient was admitted and immediately commenced on intravenous normal saline alternating with 5% dextrose in water, 1 litre every 8 hours; intravenous cefuroxime 500 mg 8 hourly; intravenous metronidazole 500 mg 8 hourly and intramuscular gentamicin 80mg 8 hourly for one week. She was transfused with one unit of cross-matched blood. A review after 6 hours showed that the patient was deteriorating clinically. There was increased pallor despite transfusion, and increased abdominal distension and tenderness. A repeated estimation of packed cell volume was 13% (haematocrit = 4 g/dL). Based on these clinical features, a provisional diagnosis was made of internal haemorrhage secondary to suspected perforation of the uterus or other viscera.

Further investigations were conducted. A pregnancy test was positive. Pelvic ultrasonography revealed an eight week live intrauterine foetus. The gestational sac and uterus were intact. A massive fluid collection was seen in the peritoneum. The confirmation of an intrauterine pregnancy and massive pelvic fluid collection changed our diagnosis. An internal haemorrhage probably due to a ruptured ectopic gestation coexisting with an intrauterine pregnancy was considered, with a working diagnosis of a heterotopic pregnancy.

The patient was subsequently prepared for emergency laparotomy and the intravenous fluid was continued as above. She was anaesthesized commencing with intravenous 50 mg ketamine, and 25mg was given as needed. The findings at laparotomy were:

  • Massive haemoperitoneum with clotted and non-clotted blood
  • A badly ruptured ectopic gestation at the ampullary portion of the right fallopian tube, still oozing blood.
  • Normal left fallopian tube
  • Intact uterus
  • All other viscera were intact.

The clotted and non-clotted blood in the peritoneum was evacuated, and a right total salpingectomy was performed.

Her BP postoperatively was 80/40 mmHg and pulse was 110 beats/ min. Two hours after surgery, her BP was 100/60mmHg and her pulse was 90 beats/ min. She had serial transfusions of two units of cross-matched blood postoperatively.

The patient sustained clinical improvement throughout the first week after surgery. She had, however, some vaginal bleeding on 10th postoperative day and a diagnosis of incomplete abortion was made with the aid of ultrasound. Gentle uterine evacuation was performed and she was discharged home on 14th postoperative day. She was seen in follow-up clinic a week after discharge. At that time she was a healthy-looking woman and her PCV was 32%. She was counseled about now having only one fallopian tube, and educated about the danger of damage to this remaining tube due to infection or a repeat ectopic pregnancy.


Heterotopic pregnancy is on the increase because of the increasing incidence of ectopic pregnancy1. The patient presented in this report had multiple sexual partners with attendant recurrent pelvic inflammatory disease (PID) which probably predisposed her to ectopic pregnancy. Tenore4 identified certain risk factors of which PID takes the lead, and multiple sexual partners were found to be associated.

Heterotopic pregnancy is associated with a very high maternal morbidity and foetal loss. This is probably due to delayed diagnosis resulting from confusing clinical features, especially when diagnostic facilities are not available5. This presentation is similar to the two cases reported by Lam et al6, the diagnoses of which were initially missed. In our patient, the history of attempted abortion with unsterilized instruments in an unhygienic environment as well as post-abortal vaginal bleeding and lower abdominal pain were suggestive more of incomplete abortion rather than ectopic pregnancy. However, the worsening clinical condition despite adequate treatment demanded further investigation. Thus, simple ultrasonography assisted in the diagnosis of heterotopic pregnancy, especially in confirming the live intrauterine foetus and co-existence of a ruptured tubal pregnancy. The use of ultrasonography, especially the three-dimensional transvaginal sonography in reproductive medicine has been reported to be useful in early diagnosis of heterotopic pregnancy7. However, such a diagnostic device is not available in our practice. A high index of clinical suspicion aided by our limited facilities prompted the quick surgical intervention.

The patient underwent multiple transfusions because she lost a large amount of blood preoperatively. This was similar to the experience of Wooley8 when he transfused his patient with seven units of blood. In addition, our patient had an abortion of her intra-uterine pregnancy. This was similar to the experience of Wooley8 but differs from the progression of the pregnancy to term and eventual normal delivery, reported in our neighbouring centres9-11. This outcome may due to the fact that the patients were managed in tertiary health centres compared with our resource-constrained rural practice. The stress of the illness due to delayed presentation may also contribute to the eventual abortion of the intrauterine pregnancy in our patient.

Nevertheless, our patient benefitted from the obstetric skills of the family physicians, although she could have been referred to a secondary health centre which was a considerable distance from our practice. The life of the patient may be endangered during transfer due to an inefficient transport system. Thus, the training of medical graduates in family medicine should be encouraged because they may be required to supplement the services of core specialists when meeting the medical needs of a large rural population, as in this case.


A high index of clinical suspicion is required for the early diagnosis of heterotopic pregnancy. This is an important lesson for rural practitioners because the diagnosis and management of heterotopic pregnancy should not be limited to the core specialists, especially in settings where such medical resources are inadequate or unavailable. A family physician should be able to attend adequately to this condition, especially in rural settings where facilities are limited. Early diagnosis by the frontline doctor and prompt treatment or immediate referral will ensure survival of the patient, and contribute positively to the achievement of the United Nations' Millennium Development Goals12.

1. Reece EA, Petrie RH, Sirmans MF, Finster M and Todd WD. Combined intrauterine and extrauterine gestations: a review. American Journal of Obstetrics and Gynaecology 1983; 146: 323-330.

2. Tat J, Haddad S, Gordon N, Timor-Trisch I. Heterotopic pregnancy after ovulation induction and assisted reproductive technologies: a literature review from 1971 to 1993. Fertility and Sterility 1996; 66: 1-12.

3. Sucov A, Deveau L, Feola P, Sculli L. Heterotopic pregnancy after in-vitro fertilization. American Journal of Emergency Medicine 1995; 13(6): 641-645.

4. Tenore JL. Ectopic pregnancy: problem-oriented diagnosis. American Family Physician 2000; 61: 1080-1088

5. Wong CM, Ganesh R, Nq KY. Ectopic pregnancy: uncommon presentations with difficulty in diagnosis. Medical Journal of Malaysia 1999; 54 (1): 117-119.

6. Lam MP, Ligrid Hung LOK, Shing-Kai YIP. Two cases of heterotopic cornual pregnancy with initially missed diagnosis. Australia and New Zealand Journal of Obstetric and Gynaecology 2004; 44(3): 256-259.

7. Raine-Fenning N, Fleischer AC. Clarifying the roles of three dimensional transvaginal sonography in reproductive medicine: an evidence based appraisal. Journal of Experimental Clinical Assisted Reproduction, 2005; 2: 10.

8. Wooley RJ. Re: Any explanation? (Online) 1999. Available: (Accessed 12 February 2008).

9. Adekanle DA, Ekomaye H, Olaitan PB. Heterotopic Pregnancy with a live female infant: a case report. The Internet Journal of Gynecology and Obstetrics. (Online) 2007; 7(1). Available: (Accessed 8 Spetember 2008).

10. El-Nafaty AU, Melah GS, Massa AA, Yahaya UR, Bukar M, Kizaya DD. Heterotopic pregnancy in a natural conception cycle. A case report. Nigerian Journal of Clinical Practice 2005; 8(2): 128-129.

11. Umezurike CC, Feyi-Waboso PA. Heterotopic pregnancy with spontaneous vaginal delivery at 36 weeks and laparotomy at term. A case report. African Journal of Reproductive Health 2005; 9(1): 162-165.

12. United Nations. Millennium Development Goals. (Online) 2008. Available: (Accessed 8 September 2008).

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