The Cancer Diaspora: A Rare Case of Pseudomyxoma Peritonei of Appendiceal Origin
- PMID: 38102072
- PMCID: PMC10725096
- DOI: 10.1177/23247096231217822
The Cancer Diaspora: A Rare Case of Pseudomyxoma Peritonei of Appendiceal Origin
Abstract
Pseudomyxoma peritonei (PMP) is a rare clinical entity characterized by widespread mucinous implants in the peritoneal cavity. Commonly seen in females in their 50s, PMP typically originates from ruptured appendiceal mucoceles that find refuge in the peritoneal space. Rarely, PMP may originate from the ovary, stomach, colon, or pancreas. Pseudomyxoma peritonei of colorectal origin is more malignant and has a lower survival rate. We report a case of a 59-year-old Hispanic woman with PMP who presented to the emergency room with a 3-month history of progressive abdominal distention. Pseudomyxoma peritonei was confirmed by computed tomography (CT) scan of the abdomen and pelvis and histopathology, and the patient underwent partial cytoreductive surgery. Given her Eastern Cooperative Oncology Group (ECOG) performance status of 1 despite extensive carcinomatosis, our patient may benefit from hyperthermic intraperitoneal chemotherapy (HIPEC) in the future.
Keywords: Pseudomyxoma peritonei; complete cytoreductive therapy; hyperthermic intraperitoneal chemotherapy; jelly belly; mucinous ascites.
Conflict of interest statement
Declaration of Conflicting InterestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
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- Galani E, Marx GM, Steer CB, Culora G, Harper PG. Pseudomyxoma peritonei : the “controversial” disease. Int J Gynecol Cancer. 2003;13(4):413-418. - PubMed
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