← Back to guidelines
Gastroenterology39 papers

Pseudomyxoma peritonei

Last edited: 4/15/2026

Overview

Pseudomyxoma peritonei (PMP) is a rare peritoneal malignancy typically originating from a perforated mucinous neoplasm of the appendix, characterized by mucinous ascites and peritoneal implants 2.

Diagnosis

  • Imaging studies (CT/MRI) to identify peritoneal masses and ascites 2.
  • Cytology analysis of peritoneal fluid to detect mucinous cells 2.
  • Histopathological examination of appendiceal tissue for mucinous adenocarcinoma 2.
  • Endoscopic evaluation may be necessary to assess the primary appendiceal lesion 2.
  • Management

  • Primary cytoreductive surgery (CRS) followed by hyperthermic intraperitoneal chemotherapy (HIPEC) is considered the standard approach for eligible patients 2.
  • Conservative management may be considered in palliative settings, including symptomatic relief with corticosteroids, antibiotics, and proton pump inhibitors 1.
  • NGT retention may be necessary despite symptoms like NGTS if drainage is critical, with careful monitoring for complications 1.
  • Special Populations

  • Palliative care settings: Individualized management focusing on symptom control, as demonstrated in cases where conservative measures effectively alleviated symptoms 1.
  • No specific guidelines provided for pregnancy, pediatrics, or elderly populations in the given abstracts [].
  • Key Recommendations

  • Perform primary cytoreductive surgery followed by HIPEC for eligible patients with PMP (Evidence: Strong 2).
  • Consider conservative management with symptomatic treatment in palliative care scenarios, especially when surgical intervention is not feasible (Evidence: Moderate 1).
  • Monitor closely for complications such as nasogastric tube syndrome in patients requiring prolonged NGT use (Evidence: Expert opinion 1).
  • References

    1 Suzuki N. Nasogastric Tube Syndrome: A Case Report of Otalgia and Hoarseness in a Palliative Care Setting. Journal of pain and symptom management 2025. link 2 Govaerts K, Lurvink RJ, De Hingh IHJT, Van der Speeten K, Villeneuve L, Kusamura S et al.. Appendiceal tumours and pseudomyxoma peritonei: Literature review with PSOGI/EURACAN clinical practice guidelines for diagnosis and treatment. European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology 2021. link

    Original source

    1. [1]
    2. [2]
      Appendiceal tumours and pseudomyxoma peritonei: Literature review with PSOGI/EURACAN clinical practice guidelines for diagnosis and treatment.Govaerts K, Lurvink RJ, De Hingh IHJT, Van der Speeten K, Villeneuve L, Kusamura S et al. European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology (2021)

    HemoChat

    by SPINAI

    Evidence-based clinical decision support powered by SNOMED-CT, Neo4j GraphRAG, and NASS/AO/NICE guidelines.

    ⚕ For clinical reference only. Not a substitute for professional judgment.

    © 2026 HemoChat. All rights reserved.
    Research·Pricing·Privacy & Terms·Refund·SNOMED-CT · NASS · AO Spine · NICE · GraphRAG