A primary peritoneal pseudomyxoma peritonei arising from the Mullerian tissue: a case report

A Ouazzani1, M Adler, N Nagy

  • 1Department of Surgery, Erasme University Hospital, Brussels, Belgium.

Acta Chirurgica Belgica
|February 16, 2008
PubMed

Insights

Pseudomyxoma peritonei is a rare condition. This case highlights the Müllerian system as a potential, overlooked origin for this enigmatic peritoneal disease, even after appendectomy.

Area of Science:

  • Gastroenterology and Oncology
  • Reproductive Medicine and Pathology

Background:

  • Primary Pseudomyxoma Peritonei (PMP) is an uncommon malignancy.
  • Historically, ovarian, colonic, and appendiceal origins were proposed for PMP.
  • Recent evidence suggests appendiceal adenoma rupture as the predominant source.

Observation:

  • A case of PMP occurred in an elderly patient with a history of childhood appendectomy.
  • The patient's condition was initially misdiagnosed as an abdominal abscess secondary to colitis.
  • This presentation challenges typical PMP origin theories.

Findings:

  • The study presents a unique case of PMP in a patient lacking a typical appendiceal origin.
  • The patient's prior appendectomy complicated the diagnostic pathway.
  • The clinical presentation mimicked infectious colitis, delaying PMP diagnosis.

Implications:

  • Metaplasia of the Müllerian system is proposed as a potential primary source for peritoneal pseudomyxoma.
  • This finding expands the differential diagnosis for PMP, especially in appendectomized patients.
  • Further research is needed to elucidate the role of Müllerian metaplasia in PMP pathogenesis.