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Updated: May 17, 2026

Culture and Imaging of Ex Vivo Organotypic Pseudomyxoma Peritonei Tumor Slices from Resected Human Tumor Specimens

Culture and Imaging of Ex Vivo Organotypic Pseudomyxoma Peritonei Tumor Slices from Resected Human Tumor Specimens

Published on: December 9, 2022

Pseudomyxoma peritonei - a case report.

T R Laila¹, S Das, S S Ahmed

¹Department of Obs & Gynae, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.

Mymensingh Medical Journal : MMJ

|November 9, 2012

Summary

Pseudomyxoma peritonei (PMP) is a rare condition. This case highlights a borderline mucinous cystadenoma presenting as abdominal swelling, successfully managed with surgery and follow-up.

Area of Science:

Gynecologic Oncology
Abdominal Surgery

Background:

Pseudomyxoma peritonei (PMP) is a rare clinical entity characterized by mucinous ascites and gelatinous implants within the peritoneal cavity.
It often originates from an appendiceal or ovarian mucinous tumor.

Observation:

A 45-year-old female presented with a 3-month history of abdominal swelling, pain, and weight loss.
Physical examination revealed a large, immobile, cystic abdominal mass with ill-defined margins.
CT scan demonstrated a pelvic cystic mass extending to the mid-abdomen with significant ascites.

Findings:

CT-guided Fine Needle Aspiration Cytology (FNAC) suggested a benign mucinous cystadenoma.
Laparotomy revealed extensive mucinous material filling the peritoneal cavity and a right ovarian tumor.

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Histopathology confirmed a borderline mucinous cystadenoma of the ovary.

Implications:

This case underscores the importance of surgical intervention for PMP, even with borderline tumors.
Complete surgical debulking and appropriate follow-up are crucial for managing PMP.
Multidisciplinary management involving gynecology, surgery, and oncology is essential for optimal patient outcomes.