Spontaneous haemoperitoneum in pregnancy (SHiP) and endometriosis: A Case Report

In: Zeitschrift für Geburtshilfe und Neonatologie · 2021 · doi:10.1055/s-0041-1739792 · W4200238803
article OA: closed CC0
Full text JSON View on OpenAlex View at publisher
AI-generated summary by claude@2026-07, 2026-07-05

This case report describes a rare instance of spontaneous hemoperitoneum in pregnancy caused by endometriosis, detailing its challenging diagnosis and successful management with a favorable outcome for mother and fetus.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-07, 2026-07-05 · read from full text

This case report describes a 39-year-old primigravida with known endometriosis who presented at 16 weeks’ gestation with sudden severe lower abdominal pain; despite stable vital signs and normal hemoglobin, ultrasound revealed free intraperitoneal fluid. Because of worsening condition and imaging findings without signs of placental abruption, the patient underwent urgent laparoscopy, which identified massive haemoperitoneum (~2000 ml clotted and fluid blood) and multiple deep peritoneal endometriosis implants. A deep parametrium left endometriosis nodule was identified as the bleeding source, leading to laparotomy for rapid hemostasis and transfusion of 4 units of red cell concentrates, after which maternal stabilization and a viable fetal outcome were maintained through delivery. As a single-patient report, it provides limited generalizability and does not establish diagnostic accuracy. This paper is centrally about endometriosis — it reports endometriosis-associated spontaneous haemoperitoneum in pregnancy, including the intraoperative identification of deep implants as the bleeding source.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

Background It is estimated that about 20% of women are affected by endometriosis. Even though endometriosis can have a negative impact on pregnancy rates, direct complications during an ongoing pregnancy caused by endometriosis are rare. Spontaneous haemoperitoneum in pregnancy (SHiP) due to endometriosis is a very uncommon but potentially life threatening situation. Preoperative diagnosis can be challenging as SHiP may not always present with clinical signs of hemorrhagic shock. We present a case which was managed in pregnancy with a favorable fetal and maternal outcome.
Full text 2,558 characters · extracted from oa-doi-fallback · 2 sections · click to expand

Background

It is estimated that about 20% of women are affected by endometriosis. Even though endometriosis can have a negative impact on pregnancy rates, direct complications during an ongoing pregnancy caused by endometriosis are rare. Spontaneous haemoperitoneum in pregnancy (SHiP) due to endometriosis is a very uncommon but potentially life threatening situation. Preoperative diagnosis can be challenging as SHiP may not always present with clinical signs of hemorrhagic shock. We present a case which was managed in pregnancy with a favorable fetal and maternal outcome. Case Report We present a case of a 39-year-old primigravida, who presented at 16 weeks with sudden onset of severe lower abdominal pain without contractions. The woman was known with the diagnosis of endometriosis and infertility for 3 years. Further medical history was clear. On admission, pain score was 8/10 (visual analog scale). The vital signs were stable. Abdominal palpation revealed a slightly distended abdomen, tenderness to deep abdominal palpation without acute peritoneal signs. The hemoglobin (Hb) level was within normal range (11.6 g/dl). The abdominal and transvaginal ultrasound showed free fluid in the pelvic cavity and in both the left and right upper abdomen. Further a viable fetus with a full biophysical profile and no signs of placental abruption was confirmed. Due to these findings and the worsening of vital signs a immediate laparoscopy was performed. Intraoperatively, a massive haemoperitoneum was confirmed with about 2000 ml of fluid and clotted blood. After aspiration, the small pelvis could be visualized revealing multiple deep endometriosis implants in the peritoneum . A deep node of endometriosis located in the parametrium left could be identified as source of bleeding. In order to achieve a fast control of the bleeding a laparotomy was performed. A total of 4 red cell concentrates were transfused. The vital signs were stabilized. Postoperatively a viable fetus could be reassured. The rest of the pregnancy and delivery passed without further complications.

Conclusion

In the differential diagnosis of acute abdomen and haemoperitoneum in the pregnancy bleeding from pelvic endometriosis has to be considered of gynecological causes. Publication History Article published online: 26 November 2021 © 2021. Thieme. All rights reserved. Georg Thieme Verlag Rüdigerstraße 14, 70469 Stuttgart, Germany

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.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Condition tags

endometriosis

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. The paper's references may be in our DB but unresolved to ``paper_id`` (resolution happens at ingest when the cited DOI matches a row we already have). Run the cross-source citation reconcile pass to retry.

Source provenance

openalex
last seen: 2026-06-10T17:14:06.276822+00:00
unpaywall
last seen: 2026-06-02T02:00:03.124865+00:00
License: CC0 · commercial use OK