Skip to main content

Idiopathic omental hemorrhage: a case report and review of the literature

Abstract

Background

A spontaneous rupture of an omental vessel can cause severe intraabdominal hemorrhage. We present a case of idiopathic omental hemorrhage caused by a vascular malformation. The literature is systematically reviewed.

Case presentation

A 65-year-old Iranian man was admitted to the emergency department for 10 days with abdominal pain. His medical history was not significant. Fever, vomiting, nausea, or anorexia were not reported. However, he was suffering from diaphoresis and malaise at the time. He did not smoke or drink alcohol. During physical examination, blood pressure was 82/60 mmHg with a temperature of 36.6 °C; heart rate was 96 beats/minute and respiratory rate was 18 breaths per/minute. An abdominal examination revealed mild tenderness in the periumblical. The focused assessment with sonography in trauma examination yielded positive results. The complete blood count showed 14 × 103/mcL of white blood cells and 185 × 103/mcL of platelets. The hemoglobin value was 6.7 g/L at admission. To stabilize the patient’s condition, a unit of packed cell was administered. A double contrast enhancement abdominal computer tomography was performed, which revealed a massive hemoperitoneum. Subsequently, an exploratory laparoscopy was performed to search for the responsible pathology. But it was not successful. The surgical plan was changed to laparotomy. The hemorrhage source was not found during laparotomy. Observation revealed a massive hemoperitoneum originating in the omental vessels. A portion of the omentum located on the greater omentum at the greater curve was removed. Based on the pathological examination of the extracted tissue, vascular malformations were identified. The patient recovered uneventfully and was discharged from the hospital 7 days after surgery. Previous reports assessing idiopathic omental bleeding were systematically reviewed. A total of 14 hits were identified in PubMed and Scopus from 2015 to November 2022 for idiopathic omental bleeding.

Conclusion

Presence of positive focused assessment with sonography in trauma, abdominal pain, imaging evidence of fluid accumulation, and a reduction in hemoglobin levels collectively indicate the likelihood of arteriovenous malformation occurrence. The treatment options include surgical intervention and transcatheter arterial embolization. Surgical intervention is recommended for subjects with hemodynamic instability, persistent hypotension and those whose diagnosis is unconfirmed.

Peer Review reports

Introduction

Idiopathic spontaneous intraperitoneal hemorrhage occurs when intraabdominal vessels rupture without an identifiable underlying cause [1].

Omental bleeding may occur due to trauma-associated injury and irritation, neoplasia [2], arterial aneurysm rupture [3], and anticoagulant treatment [4].

Due to their rarity, therapeutic management guidelines are not yet established. We present a case of idiopathic omental hemorrhage caused by a vascular malformation. A systematic review of previous reports was also conducted.

Case presentation

A 65-year-old Iranian man arrived at the emergency department complaining of abdominal pain for 10 days with no history of recent trauma. Additionally, he suffered from diaphoresis and malaise. He had no significant previous medical history. Hematochezia, melena, anorexia, vomiting, nausea, or fever were not present. He was a non-smoker and non-alcoholic. Physical examination revealed 82/60 mmHg blood pressure, a temperature of 36.6 °C, and heart and respiratory rates of 96 beats and 18 breaths per minute, respectively. Examination of the abdomen showed symmetry without any scars. The abdominal assessment revealed only tenderness in the periumbilical region, and auscultation detected normal intestinal sounds. The focused assessment with sonography in trauma (FAST) examination yielded positive results. The complete blood count (CBC) reported white cell and platelet counts of 14 × 103/L and 185 × 103/L, respectively. Hemoglobin was 6.7 g/L at admission. One unit transfusion of packed cells was done. As soon as the patient was stable, a double contrast enhancement abdominal computer tomography (CT) was performed, which revealed massive hemoperitoneum. Through abdominal CT, we were unable to identify the source of bleeding. Hemoperitoneum was proved by ascitic tap ultrasound. During hospitalization, the hemoglobin value decreased by 2 units in 5 days. Subsequently, an exploratory laparoscopy was performed, searching for the responsible pathology. Approximately 2 L of blood was suctioned. But it was not successful. So, the surgical plan was changed to laparotomy. During laparotomy no active hemorrhage source was found. There was only a slight change (the lesion-like hematoma was 3 mm in size) in apparent omentum. Our decision was to take a biopsy of the omentum located on the greater omentum at the greater curve and send it for pathology analysis. Pathological assessment of the extracted tissue pointed to abnormally dilated blood vessels—an arteriovenous malformation (AVM) (Fig. 1). A 7-day hospital discharge followed the patient’s uneventful recovery. We performed follow-ups for the patient at the hospital outpatient department at 6 months intervals. The follow-up after 3 months showed that the patient had no signs of recurrence (Fig. 2). The timeline from emergency to follow-up is presented in Fig. 2.

Fig. 1
figure 1

Abnormally dilated blood vessels, an arteriovenous malformation (AVM)

Fig. 2
figure 2

Timeline from emergency to follow-up in a patient who is suspected of AVM

Review of the literature

PubMed and Scopus (2015–2022) databases were searched for case reports of idiopathic omental bleeding. Screening was conducted on all abstracts published in the English language. Data on patient characteristics, including age, diagnosis, and treatment, were extracted.

Out of the 12 articles, one of them contained three cases of idiopathic omental bleeding, which we have included in our study [5,6,7,8,9,10,11,12,13,14,15,16]. The relevant findings are summarized in Table 1. Patients ranged in age from 22 to 73 years old, including 10 males and 4 females. An abdominal CT scan, magnetic resonance imaging (MRI), an abdominocentesis, and a laparotomy were used in the diagnostic procedure. The patients underwent emergency surgery (n = 7) or transcatheter arterial embolization (TAE) (n = 4), and one patient underwent both. Five patients underwent omentectomy and three had ligation, all of which achieved hemostasis. One patient was managed non-operatively as a conservative case [5].

Table 1 Reports of idiopathic omental hemorrhage

Discussion

Omental bleeding, with a mortality rate exceeding 30%, is a serious condition [17]. The mortality rate of 30% could be linked to the delayed diagnosis of most cases. It is worth mentioning that only a small number of cases were accurately diagnosed prior to treatment, which may have played a role in the elevated mortality rate.

FAST is frequently employed to expedite the prompt identification of life-threatening hemorrhage in patients. The majority of patients with positive FAST results require laparotomy [18].

Idiopathic omental bleeding requires aggressive treatment, regardless of its underlying cause. Omentectomy or ligation are routine surgical procedures for idiopathic omental hemorrhage. Most reported cases, however, involved emergency surgery. The surgical option is suitable for patients with persistent hypotension and unconfirmed diagnoses. The reason why surgery is often needed is that few cases are diagnosed correctly before treatment [12].

Vascular malformations (VMs) are treated with surgery and embolization. Embolization through endovascular means is less invasive and recommended in most cases. Life-threatening conditions can arise due to VMs because of their unpredictable clinical evolution and manifestations [19].

The cases presented in this manuscript are spontaneous, with no history of trauma, coagulopathy, or comorbidities, except for two [6, 7]. Abdominal pain was reported by all patients. LUQ, RUQ, and upper greater omental are the most common sites of bleeding.

Omental hemorrhage commonly presents in male patients with abdominal pain and occasionally with nausea, vomiting, or diarrhea. However, some of our included cases may not have had any other abdominal symptoms [6, 8,9,10,11,12,13].

Ultrasonography, computed tomography scan with contrast, chest x-ray [5], angiography [6], MRI with contrast, and paracentesis [5] may be useful to establish the diagnosis.

Optimal diagnostic and therapeutic evidence for spontaneous intraperitoneal hemorrhage remains controversial, based on the available literature. Through our case analysis and literature review, it has been observed that the prevailing diagnostic model for arteriovenous malformation primarily relies on the presence of positive FAST, abdominal pain, imaging evidence of fluid accumulation, and a reduction in hemoglobin levels, all of which collectively indicate the likelihood of AVM occurrence. CT angiography (CTA) may have false negative results, however, due to short acquisition times when bleeding is not obvious at time of scan [20]. It has been described that transcatheter arterial embolization is a definitive treatment [21].

A laparotomy or laparoscopy coupled with an omentectomy or a simple artery ligation is recommended. Laparoscopic surgery or transcatheter arterial embolization have been used more frequently in recent years as minimally invasive interventions [21, 22].

As described in the report, a patient presented to our hospital with sudden, non-specific abdominal pain, which was diagnosed with idiopathic spontaneous intraperitoneal hemorrhage caused by a vascular malformation in the omentum.

Conclusion

A spontaneous intraabdominal hemorrhage without any antecedent trauma should begin with volume resuscitation to stabilize the patient’s circulatory parameters. Coagulation studies and platelet function analysis should be considered. Hemorrhages of the omentum, however, are infrequent, and patients’ conditions are often unstable. In cases where no source of bleeding is found, a high index of suspicion should be kept. Presence of positive FAST, abdominal pain, imaging evidence of fluid accumulation, and a reduction in hemoglobin levels collectively indicate the likelihood of AVM occurrence. The venous hypertension, which can be caused by factors such as consuming food or engaging in extensive sports, can lead to reduced perfusion pressure in the surrounding tissues. For both unconfirmed and definitive diagnoses and treatments, emergency surgery is recommended. To rule out underlying malignancy or vascular disease, omentectomy is preferred to ligation or transcatheter arterial embolization. Rebleeding should be eliminated from these patients by omentectomy as a definitive therapy.

Availability of supporting data

Not applicable.

Abbreviations

FAST:

Focused assessment with sonography in trauma

CBC:

Complete blood count

CT:

Computer tomography

TAE:

Transcatheter arterial embolization

AVM:

Arteriovenous malformation

MRI:

Magnetic resonance imaging

VMs:

Vascular malformations

CTA:

CT angiography

References

  1. Varzgalis M, et al. Spontaneous rupture of the inferior pancreatoduodenal artery: case report and literature review. MOJ Surg. 2015;2(2):00017.

    Google Scholar 

  2. Dixon AY, et al. Primary omental leiomyosarcoma masquerading as hemorrhagic ascites. Hum Pathol. 1984;15(3):233–7.

    Article  CAS  PubMed  Google Scholar 

  3. Borioni R, et al. Hemoperitoneum due to spontaneous rupture of an aneurysm of the left gastroepiploic artery. J Cardiovasc Surg. 1999;40(1):63–4.

    CAS  Google Scholar 

  4. Adelman M, et al. Localised intramesenteric haemorrhage—a recognisable syndrome in haemophilia? BMJ. 1979;2(6191):642.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Zhu J, et al. A case report of spontaneous lesser omental haemorrhage. Hong Kong J Emerg Med. 2015;22(1):53–6.

    Article  Google Scholar 

  6. Moriarty HK, et al. Omental apoplexy: unravelling the mystery. J Med Imaging Radiat Oncol. 2020;64(3):319–25.

    Article  PubMed  Google Scholar 

  7. Viñas J, et al. Haemoperitoneum caused by spontaneous haemorrhage of the greater omentum: a rare complication occurring in a patient with severe SARS-CoV-2 infection. Ann R Coll Surg Engl. 2021;103(8):e266–8.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Maghrebi H, et al. Spontaneous rupture of a left omental artery aneurysm treated by transcatheter arterial embolization: a case report. Ann Med Surg. 2022;82: 104704.

    Article  Google Scholar 

  9. Furukawa K, et al. Gastrointestinal: idiopathic omental hemorrhage. J Gastroenterol Hepatol. 2022;37(2):282–282.

    Article  CAS  PubMed  Google Scholar 

  10. Takayama S, et al. Idiopathic omental bleeding treated by laparoscopic partial omentectomy: a case report and review of the literature. Cureus. 2021. https://doi.org/10.7759/cureus.15795.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Wu Y-H, Liu K-T, Wen C-K. A rare diagnosis of abdominal pain presentation in the emergency department: idiopathic omental bleeding: a case report. Medicine. 2017;96(51): e9463.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Lyu Y-X, Cheng Y-X, Li T. Spontaneous omental bleeding: a case report and literature review. BMC Surg. 2018;18(1):1–4.

    Article  CAS  Google Scholar 

  13. Kimura J, et al. Idiopathic omental hemorrhage: a case report and review of the literature. Int J Surg Case Rep. 2016;28:214–8.

    Article  PubMed  PubMed Central  Google Scholar 

  14. McClintock CM, et al. Visceral artery aneurysmal lesion of the omentum—a rare cause of spontaneous fatal intra-abdominal hemorrhage. Forensic Sci Med Pathol. 2022;18(4):470–3.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Hosotani T, et al. A case of idiopathic omental hemorrhage. Gynecol Minim Invasive Ther. 2016;5(2):88–90.

    Article  Google Scholar 

  16. Zhou Y, et al. Idiopathic spontaneous intraperitoneal hemorrhage due to vascular malformations in the muscularis of the stomach: a case report. Front Med. 2022;9: 927899.

    Article  Google Scholar 

  17. Lucey BC, et al. Spontaneous hemoperitoneum: a bloody mess. Emerg Radiol. 2007;14:65–75.

    Article  PubMed  Google Scholar 

  18. Barbosa RR, Rowell SE, Fox EE, Holcomb JB, Bulger EM, Phelan HA, Alarcon LH, Myers JG, Brasel KJ, Muskat P, Del Junco DJ, Cotton BA, Wade CE, Rahbar MH, Cohen MJ, Schreiber MA. Increasing time to operation is associated with decreased survival in patients with a positive FAST examination requiring emergent laparotomy. J Trauma Acute Care Surg. 2013;75:S48–52.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Vickers NJ. Animal communication: when i’m calling you, will you answer too? Curr Biol. 2017;27(14):R713–5.

    Article  CAS  PubMed  Google Scholar 

  20. Mitreski G, et al. STABILISE; treatment of aortic dissection, a single centre experience. CVIR Endovasc. 2022;5(1):1–10.

    Article  Google Scholar 

  21. Takahashi M, et al. Spontaneous rupture of the omental artery treated by transcatheter arterial embolization. Case Rep Radiol. 2012. https://doi.org/10.1155/2012/273027.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Matsumoto T, et al. Transcatheter arterial embolization for spontaneous rupture of the omental artery. Cardiovasc Intervent Radiol. 2011;34:142–5.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The authors of this manuscript declare no relationships with any companies whose products or services may be related to the subject matter of the article. We thank the patients who participated in this study.

Funding

We do not have any financial support for this study.

Author information

Authors and Affiliations

Authors

Contributions

FR and AS contributed in the searching, extraction and drafting of the manuscript. NJ contributed to editing and revising manuscript. RH contributed in the developing idea.

Corresponding author

Correspondence to Reza Hajebi.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Competing interests

The authors declare no conflict of interest regarding the publication of this paper.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Rashidi, F., Samimiat, A., Jafarimehrabady, N. et al. Idiopathic omental hemorrhage: a case report and review of the literature. J Med Case Reports 17, 368 (2023). https://doi.org/10.1186/s13256-023-04112-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13256-023-04112-8

Keywords