Abstract
Background: Spontaneous hemoperitoneum in pregnancy (SHiP) is a rare but life-threatening condition associated with maternal and perinatal mortality. Herein,
we report a case of intra-abdominal hemorrhage caused by spontaneous utero-ovarian vessel rupture at 27 gestational weeks following surgery two years earlier for
severe endometriosis.
Case: A 31-year-old woman primigravida presented to the hospital at 27 weeks’ gestation with acute abdominal pain. She had a history of laparoscopy for severe
endometriosis and bilateral ovarian endometriomas. Although the initial ultrasound done was normal, there was a clinical suspicion of hemoperitoneum in pregnancy,
which was confirmed by MRI. An emergency laparotomy was performed.
Results
About 2000 mL of blood in the abdominal cavity was evacuated. Cesarean section was performed at the same time due to difficulty in hemostasis and
difficulty in securing the field of vision. Extensive adhesions including both adnexa tightly adhered to the posterior surface of the uterus and completely obliterated
pouch of Douglas behind the uterus were noted. Active bleeding from the left-posterior uterine-ovarian vessels was found and hemostasis was achieved.
Conclusions
If pregnant women with a history of previous endometriosis treatment present with acute abdominal pain, a fall in hemoglobin, and the absence of
vaginal bleeding, intraabdominal hemorrhage should be considered.
*Correspondence to: Heesuk Chae, Department of Obstetrics and Gynecology,
Chonbuk National University Hospital, Jeonju, South Korea, Tel: 821062644762;
E-mail:
[email protected]
Key words: endometriosis, pregnancy, spontaneous hemoperitoneum
Received: October 10, 2020; Accepted: October 16, 2020; Published: October
20, 2020
Introduction
Spontaneous hemoperitoneum in pregnancy (SHiP) is a rare but
almost always life-threatening condition associated with high maternal
and perinatal mortality [1,2]. This situation occurs mainly in the second
and third trimester of pregnancy [3]. The etiology of this condition is
unknown, but recently, it is believed to be related to endometriosis
[1,3,4]. We report a case of SHiP complicated by endometriosis.
Case
A 31-year-old woman primigravida presented to the hospital
at 27 weeks’ gestation with acute abdominal pain. Besides previous
pelvic surgery which she had received laparoscopy because of severe
endometriosis and bilateral ovarian endometriomas two years
previously, she was otherwise healthy. Her antenatal course had been
uneventful. The patient’s main symptom started during a defecation
attempt.
On admission, her blood pressure and heart rate were 120/70
mmHg and 77 beats/min, respectively. Her circulating hemoglobin
level was 8.6 g/dL. On examination, she had a soft abdomen with
slight tenderness on gentle palpation. There were no signs of vaginal
bleeding or vaginal discharge. The cervix was closed. Cardiotocogram
demonstrated no uterine contractions and showed fetal heart rate with
normal variability. Ultrasound imaging showed normal amniotic fluid
volume and a placenta without any signs of abruption.
The following day the patient’s clinical condition abruptly worsened
when she tried to stool again. Blood pressure was 80/50 mmHg and
the hemoglobin level decreased to 6.0 g/dL. Magnetic resonance image
(MRI) revealed massive intra-abdominal fluid collection (Figure 1A
and 1B).
An emergency laparotomy was performed. Intraoperatively, almost
2,000 mL of blood and clots were noted. However, because of the gravid
uterus, it was difficult to find the bleeding site, so caesarean section
was decided. A female baby weighing 905 g was extracted. The Apgar
scores were 1 and 3 at 1 and 5 minutes, respectively. Both adnexa were
tightly adhered to the posterior surface of the uterus and completely
Figure 1(A). Transverse MR image shows perihepatic hemoperitoneum. (B) Coronal MR
image shows fluid collection in the abdomen
Sim Y (2020) Spontaneous hemoperitoneum in pregnancy (SHiP) complicated by endometriosis: A case report
Volume 4: 2-2
Obstet Gynecol Rep, 2020 doi: 10.15761/OGR.1000150
Conclusion
In conclusion, as shown in our case, the presence of endometriosis
may be a risk factor for SHiP. If pregnant women with a history of
endometriosis had development of conditions of sudden abdominal
pain, a reduction of hemoglobin, and the absence of vaginal bleeding,
even if rare, obstetricians should bear in mind the possibility of SHiP.
Acknowledgment
Thank numerous individuals participated in this study.
Authors disclosure statement
The authors have no conflicts of interest to declare.
References
1. Brosens IA, Fusi L, Brosens JJ (2009) Endometriosis is a risk factor for spontaneous
hemoperitoneum during pregnancy. Fertil Steril 92: 1243-1245.
2. Katorza E, Soriano D, Stockheim D, Mashiach R, Zolti M, et al. (2007) Severe intra-
abdominal bleeding caused by endometriotic lesions during the third trimester of
pregnancy. Am J Obstet Gynecol 197: 501.e1-e4.
3. Lier M, Malik RF, van Waesberghe J, Maas JW, van Rmpt-van de Geest DA, et al.
(2017) Spontaneous haemoperitoneum in pregnancy and endometriosis: a case series.
BJOG 124: 306-312.
4. Inoue T, Moriwaki T, Niki I (1992) Endometriosis and spontaneous rupture of utero-
ovarian vessels during pregnancy. Lancet 340: 240-241.
5. Maggiore ULR, Ferrero S, Mangili G, Bergamini A, Giorgione V, et al. (2016) A
systematic review on endometriosis during pregnancy: diagnosis, misdiagnosis,
complications and outcomes. Hum Reprod Update 22: 70-103.
6. Passos F, Calhaz-Jorge C, Graca LM (2008) Endometriosis is a possible risk factor
for spontaneous hemoperitoneum in the third trimester of pregnancy. Fertil Steril 89:
251-252.
7. Loi ES, Darwish B, Abo C, Millischer-Bellaiche AE, Angioni S, et al. (2016) Recurrent
hemoperitoneum during pregnancy in large deep endometriosis infiltrating the
parametrium. J Min Invasive Gynecol 23: 643-646.
8. Wada S, Yoshiyuki F, Fujino T, Sato C (2007) Uterine vein rupture at delivery as a
delayed consequence of laparoscopic surgery for endometriosis: a case report. J Minim
Invasive Gynecol 14: 463-469.
9. Cozzolino M, Corioni S, Maggio L, Sorbl F, Guaschino S, et al. (2015) Endometriosis-
related hemoperitoneum in pregnancy: a diagnosis to keep in mind. The Ochsner J 15:
262-264.
10. Wu CY, Hwang JL, Lin YH, Hsieh BC, Seow KM, et al. (2007) Spontaneous
hemoperitoneum in pregnancy from a ruptured superficial uterine vessel. Taiwan J
Obstet Gynecol 46: 77-80.
11. Kapila P (2011) Fatal non-traumatic spontaneous hemoperitoneum in second trimester
of pregnancy-autopsy findings. J Forensic Leg Med 18: 139-140.
12. O’Leary SM (2006) Ectopic decidualization causing massive postpartum intraperitoneal
hemorrhage. Obstet Gynecol 108: 776-779.
obliterated pouch of Douglas were observed. Active bleeding was found
in the fragile veins at the left-posterior uterine-ovarian vessels, which
was then sutured for hemostasis. During surgery, the patient received 3
units of red blood cells and 2 units of cryoprecipitate. The patient had
an uneventful course and was discharged 6 days after the operation.
The infant was transferred to an intensive care unit and was discharged
10 weeks after birth.
Discussion
Spontaneous hemoperitoneum in pregnancy (SHiP) is a relatively
rare condition associated with maternal and perinatal mortality [1,5].
Furthermore, as in the first case, hemoperitoneum in pregnancy
resulting from spontaneous rupture of uterine-ovarian vessels is
extremely rare. During the past 20 years over 25 cases of SHiP have
been reported, occurring during the antepartum (61%), labor (18%),
and early postpartum periods (21%) [6,7].
The cause of the condition remains poorly understood. However,
several etiologic factors have been proposed: increase in venous
pressure in the uteroovarian circulation, resulting from the physiologic
demands of pregnancy and during muscular activity and straining, such
as coughing, defecation, coitus, or during the pushing phase of second
stage labor [2]. However, a series of recent reports have been suggested
that endometriosis may cause SHiP. Hemoperitoneum in pregnant
women with endometriosis can be caused by spontaneous rupture of
utero-ovarian vessels or direct bleeding of endometriosis implants.
Inoue, et al. suggested first that endometriosis might be a possible
risk factor for SHiP [4]. Friable uterine vessels resulting from chronic
inflammation accompanied by endometriosis or vessel tension resulting
from adhesion presumably contributes to vessel rupture [4,8]. Brosens,
et al. noticed that SHiP was associated with endometriosis in >50% of
cases [1]. The pathologic examination of the site of bleeding during
pregnancy confirmed endometriosis, characterized by prominent
vascularization and decidualization of the lesion [1,9]. We agree with
Inoue’s hypothesis based on the facts that severe endometriosis was
observed at the time of surgery and hemoperitoneum due to spontaneous
rupture of the uterine vessels rather than endometriosis lesions occurred.
The uterine vessels weakened by endometriosis cause rupture when
intraabdominal pressure during physical activity such as defecation.
The diagnosis of SHiP is rarely made before laparotomy due to their
extreme rarity and it is frequently misdiagnosed as placental abruption.
Other differential diagnoses include uterine rupture, ruptured
appendix, abdominal pregnancy, ruptured vasculature of the liver or
spleen, and HELLP syndrome [10]. In addition, a correct preoperative
diagnosis based on a clinical entity is difficult because SHiP is usually
related to non-specific symptoms of acute abdominal pain, vomiting
and maternal anemia [3]. This explains a higher rate of maternal and
perinatal mortalities of SHiP [11,12].
Copyright: ©2020 Sim Y. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use,
distribution, and reproduction in any medium, provided the original author and source are credited.
Text is read by the "Ask this paper" AI Q&A widget below.
Extraction quality varies by source — PMC NXML preserves structure
cleanly, OA-HTML may include some navigation residue, and OA-PDF can
have broken hyphenation. The publisher copy
(via DOI)
is the canonical version.