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Eastern Mediterranean Health Journal

versão impressa ISSN 1020-3397

East. Mediterr. health j. v.13 n.4 Cairo julho/ago. 2007

 

CASE REPORT

 

Spontaneous ruptured and intact bilateral tubal ectopic pregnancy

 

 

G.A. Al-Quraan; M.I. Al-Taani; B.M. Nusair; A. El-Masri; M.R. Arafat; M.M. Khateeb

Royal Medical Services, Amman, Jordan (Correspondence to M.I. Al-Taani: maltaani@yahoo.com). Received: 23/06/05; accepted: 15/08/05

 

 

Case report

A 35-year-old Iraqi woman (gravida 7, para 5 + 1 abortion) was admitted to the Jordanian field hospital in Fallujah, Iraq in January 2004 with a history of 8 weeks amenorrhoea; intermittent vaginal bleeding and mild lower abdominal pain of 4 weeks duration; and a positive urine pregnancy test on the day of admission. She had been married for 13 years. Her menstrual history was not relevant. There was no past history of contraception use or previous abdomino-pelvic surgery.

General examination revealed maternal tachycardia (pulse 110 per minute), hypotension (systolic/diastolic blood pressure 90/60 mmHg) and pallor. Her abdomen was tender on palpation with positive rebound and guarding.

On pelvic examination, there was mild spotting, the cervical os was closed and the cervix tender on transverse motion. The uterus was bulky; there was fullness in all the fornices with tenderness; and the adnexae were difficult to palpate. Haematological examination showed: white cell count 8 × 109 cells/L, haemoglobin 8.5 g/dL and haematocrit 25%. Pelvic ultrasound examination showed bulky uterus, homogenous texture and mild thick endometrium with smooth outline. A moderate amount of fluid collection was present in the pouch of Douglas.

Emergency exploratory laparotomy revealed haemoperitoneum of approximately 800 mL. There was a ruptured fimbrial ectopic pregnancy with active bleeding on the right side. The left tube showed an intact ectopic pregnancy 2 cm × 2 cm in the ampullary region that was bleeding and forming an organized haematoma at the fimbrial end (Figure 1).

In view of these findings, right salpingectomy and left salpingostomy with cautery were carried out with removal of the product of conception. The patient received 2 units of type O Rh positive blood. Postoperative follow-up was uneventful and the patient was discharged on the 5th day post-operation.

Two weeks after surgery the beta subunit of human chorionic gonadotrophin was zero.

Histopathological examination of the specimens, excised right ruptured tube and the product of conception extracted from the left tube, confirmed the diagnosis. It revealed tubal tissues with decidua and chorionic villi on the right ruptured tube. Inflamed decidua with chorionic villi, but no tubal tissues, were seen on the specimen from the left side.

 

Discussion

Spontaneous bilateral ectopic pregnancy is rare, therefore preoperative diagnosis is uncommon. The frequency of bilateral ectopic pregnancy has been estimated at 1/200 000 uterine pregnancies and 1/725-1/1580 ectopic pregnancies. [1]. In the past 20 years a 3-fold increase in the incidence has been observed. [2] Heterotopic as well as bilateral tubal ectopic pregnancies are seen after the introduction of assisted reproductive treatment [3,4,5,6]. The occurrence of spontaneous bilateral ectopic pregnancy is, however, exceedingly rare [1,7,8].

We report a very rare case of spontaneous ruptured and intact bilateral ectopic pregnancy involving the ampullary segments. This case met the findings for simultaneous tubal pregnancy by the presence of either embryos of similar age or chorionic villi in both fallopian tubes at the time of surgery [9,10]. Ultrasonography in our case failed to make such a diagnosis and this is in agreement with other reports, i.e the use of ultrasound is not necessary to make a diagnosis in bilateral ectopic pregnancy [8,11]. Therefore, diagnosis of ectopic pregnancy continues to be an important challenge facing emergency physicians.

Our findings in this case are similar to those of Kansaria, Chauhan and Mayadeo, who reported a right ruptured fimbrial ectopic and left chronic ruptured tubal ectopic pregnancy [12]. Surgical management to preserve the left tube was by excision of the haematoma along with a thin rim of the tube; haemostasis was achieved by under-running the salpingostomy incision. In the case we describe here, only linear salpingostomy using cautery for haemostasis was done and there was no need to suture the site of incision. In both cases right salpingectomy was performed.

Careful attention should be directed to follow-up tests. A serial measurement of serum concentrations of human chorionic gonadotrophin is necessary to rule out the risk of persistent trophoblast. Since no single postoperative concentration of humanchorionic gonadotrophin is prognostic,
follow-up until completeresolution is necessary [13]. Further medical treatment with methotrexate or surgery in symptomatic patients may be necessary if humanchorionic gonadotrophin levels do not decline or persist.

Since the woman’s future ability to reproduce may be adversely affected, we would argue the necessity of carefully examining both adnexae at the time of exploratory laparotomy undertaken for suspicion of ectopic pregnancy, as proposed by others [10,14,15].

 

References

1. Adair CD et al. Bilateral tubal ectopic pregnancies after bilateral partial salpingectomy. A case report. Journal of reproductive medicine, 1994, 39(2):131-3.

2.   Stabile I, Grudzinskas JG. Ectopic pregnancy: a review of incidence, etiology, and diagnostic aspects. Obstetrical and gynecological survey, 1990, 45(6):335-47.

3.   Rizk B et al. Rare ectopic pregnancies after in vitro fertilization: one unilateral and four bilateral tubal pregnancies. Human reproduction, 1990, 5(8):1025-8.

4.   Olive DL et al. Gamete intrafallopian transfer (GIFT) complicated by bilateral ectopic pregnancy. Fertility and sterility, 1988, 49(4):719-20.

5.   Zouves C, Erenus M, Gomel V. Tubal ectopic pregnancy after in vitro fertilization and embryo transfer: a role for proximal occlusion or salpingectomy after failed distal tubal surgery? Fertility and sterility, 1991, 56(4):691-5.

6.   Abramovici D et al. Bilateral ectopic pregnancy. A case report. Journal of the Kentucky Medical Association, 1995, 93(7): 295.

7.   Kahraman S et al. Simultaneous bilateral tubal pregnancy after intracytoplasmic sperm injection. Human reproduction, 1995, 10(12):3320-1.

8.   Messore M et al. Spontaneous left tubal and right interstitial pregnancy: A case report. Journal of reproductive medicine, 1997, 42(7):445-7.

9.   Al-Awwad MM, al Daham N, Eseet, JS. Spontaneous unruptured bilateral ectopic pregnancy: conservative tubal surgery. Obstetrical and gynecological survey, 1999, 54(9):543-4.

10.  Mathew M, Saquib S, Krolikwski A. Simultaneous bilateral tubal pregnancy after ovulation induction with clomiphene citrate. Saudi medical journal, 2004, 25(12):2058-9.

11.  O’Brien MC, Rutherford T. Misdiagnosis of bilateral ectopic pregnancies: a caveat about operator expertise in the use of transvaginal ultrasound. Journal of emergency medicine, 1993, 11(3):275-8.

12.  Kansaria J, Chauhan A, Mayadeo N. An unusual case of bilateral tubal ectopic pregnancy. Bombay hospital journal, 2002, 44(1) (http://bhj.org/journal/2002-4401-jan/case-116.htm, accessed 5 November 2006).

13.  Jimenez-Caraballo A, Rodriguez-Donoso G. A 6-year clinical trial of methotrexate therapy in the treatment of ectopic pregnancy. European journal of obstetrics, gynecology and reproductive biology, 1998, 79(2):167-71.

14.  Sherman SJ, Werner M, Husain M. Bilateral ectopic gestations. International journal of gynaecology and obstetrics, 1991, 35(3):255-7.

15.  Suwajanakorn S et al. Bilateral tubal pregnancy following in vitro fertilization and embryo transfer. Journal of the Medical Association of Thailand, 1996, 79(1):40-3.