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Culture and Imaging of Ex Vivo Organotypic Pseudomyxoma Peritonei Tumor Slices from Resected Human Tumor Specimens
Published on: December 9, 2022
[A Case of Appendiceal Pseudomyxoma Peritonei Diagnosed by Inguinal Hernia and Treated with Multidisciplinary
Akira Sogawa1, Takashi Matsunaga, Yasumitsu Oe
1Dept of Digestive Surgery and Peritoneal Dissemination Center, Omi Medical Center.
Abstract:
Pseudomyxoma peritonei (PMP)is a clinical condition caused by ruptured mucinous tumors like appendix and ovaries, and large amounts of mucus fill the abdominal cavity. We experienced a case of PMP presented with an inguinal hernia. A 62-year-old man complained of a bulge in the left inguinal region. The results of the test was PMP caused by ruptured appendiceal myxoma. After intraperitoneal chemotherapy, we performed surgery. We performed right hemicolectomy, low anterior resection, peritoneum excision of the pelvic space, right diaphragm resection, omentectomy, cholecystectomy and splenectomy. Finally, hyperthermia chemotherapy was performed. Microscopic findings showed PMP caused by low-grade appendiceal mucinous neoplasm. We report this case with some bibliographic consideration.
Insights
Pseudomyxoma peritonei (PMP), a rare condition caused by ruptured mucinous tumors, was diagnosed in a patient presenting with an inguinal hernia. This case highlights PMP originating from appendiceal myxoma, requiring extensive surgical and chemotherapeutic intervention.
Area of Science:
- Gastroenterology
- Oncology
- Surgical Pathology
Background:
- Pseudomyxoma peritonei (PMP) is a rare clinical condition characterized by mucinous tumor rupture, leading to mucus accumulation in the abdominal cavity.
- PMP commonly arises from appendiceal or ovarian mucinous tumors.
- Inguinal hernias are uncommon presenting symptoms for PMP.
Purpose of the Study:
- To report a unique case of PMP presenting as an inguinal hernia.
- To discuss the diagnostic and therapeutic challenges of PMP.
- To review relevant literature concerning PMP and inguinal hernias.
Main Methods:
- A case study of a 62-year-old male with a left inguinal bulge was investigated.
- Diagnostic workup confirmed PMP originating from a ruptured appendiceal mucinous neoplasm.
- Treatment involved extensive cytoreductive surgery and hyperthermia chemotherapy.
Main Results:
- The patient was diagnosed with PMP secondary to a low-grade appendiceal mucinous neoplasm.
- Surgical procedures included right hemicolectomy, low anterior resection, and extensive peritoneal and organ resections.
- Postoperative hyperthermia chemotherapy was administered.
Conclusions:
- PMP can present with atypical symptoms such as inguinal hernias.
- A multidisciplinary approach involving surgery and chemotherapy is crucial for managing PMP.
- Early diagnosis and comprehensive treatment are vital for improving patient outcomes in PMP.
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