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Updated: Apr 6, 2026

Culture and Imaging of Ex Vivo Organotypic Pseudomyxoma Peritonei Tumor Slices from Resected Human Tumor Specimens
Published on: December 9, 2022
Pseudomyxoma peritonei extending to the lower extremity: a case report
Min Wook Joo1, Yang-Guk Chung2, Soo Young Hur3
1Department of Orthopaedic Surgery, College of Medicine, St. Vincent's Hospital, The Catholic University of Korea, Jungbu-daero 93, Paldal-gu, Suwon-si, Gyeonggi-do, 442-723, Republic of Korea. mwjoo@catholic.ac.kr.
Pseudomyxoma peritonei is a rare condition of mucinous ascites. This case highlights an unusual lower extremity extension, challenging diagnostic and management strategies for this rare malignancy.
Area of Science:
- Oncology
- Gastroenterology
Background:
- Pseudomyxoma peritonei (PMP) is defined by mucinous ascites from a mucin-producing neoplasm, though its definition remains debated.
- PMP can lead to cachexia and death due to intestinal obstruction as tumor deposits engulf the abdominal cavity.
Observation:
- A unique case of PMP in an 80-year-old woman presented with extensive tumor deposits reaching the lower extremity, mimicking an infectious process.
- Despite a histologic subtype typically associated with a poor prognosis, the patient survived long-term without bowel obstruction.
Findings:
- The lower extremity lesion was managed with limited, extensive surgery.
- The precise origin of the PMP and the mechanism of its unusual extension to the extremity were not elucidated in this case.
Implications:
- This case underscores the importance of recognizing PMP and its rare presentations, such as extremity involvement.
- Further research is needed to clarify the disease mechanisms and establish optimal management strategies for such unusual PMP cases.
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