The Cancer Diaspora: A Rare Case of Pseudomyxoma Peritonei of Appendiceal Origin.
Lefika BathobakaeSacide S OzgurMohita JariwalaJaydev KesraniShajla AjasMehandar KumarAmer AkmalPublished in: Journal of investigative medicine high impact case reports (2024)
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.
Keyphrases
- computed tomography
- low grade
- rare case
- case report
- dual energy
- positron emission tomography
- minimally invasive
- image quality
- public health
- multiple sclerosis
- magnetic resonance imaging
- high grade
- papillary thyroid
- healthcare
- south africa
- emergency department
- coronary artery bypass
- magnetic resonance
- locally advanced
- squamous cell carcinoma
- coronary artery disease
- surgical site infection
- endovascular treatment
- acute coronary syndrome
- childhood cancer
- rectal cancer
- metastatic renal cell carcinoma
- abdominal aortic aneurysm