Intraperitoneal and Appendiceal Malignancies Open access Peer reviewed

Pseudomyxoma peritonei from independent primary ovarian and appendiceal tumors: a case report

Jiyeon Koo, Long Ngo Hoang, Mi Kyung Kim, Rae Rim Ryu and 3 more

Journal of Yeungnam Medical Science | Sep 4, 2026

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An 83-year-old woman presented with abdominal distension and ascites incidentally discovered during an evaluation for traumatic intracranial hemorrhage and underwent diagnostic laparoscopy, which confirmed the presence of gelatinous ascites, which was consistent with PMP.

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Pseudomyxoma peritonei (PMP), which involves both the ovaries and appendix, is usually attributed to an appendiceal primary tumor with secondary involvement. However, rare cases may present with synchronous, independent mucinous primaries. Distinguishing between these entities is important because staging, treatment, prognosis, and follow-up may differ according to the primary site. An 83-year-old woman presented with abdominal distension and ascites incidentally discovered during an evaluation for traumatic intracranial hemorrhage. Computed tomography revealed large-volume ascites, a large multilocular cystic mass arising from the left ovary, and a dilated appendix. Diagnostic laparoscopy confirmed the presence of gelatinous ascites, which was consistent with PMP. Histopathological examination revealed ovarian mucinous carcinoma and appendiceal mucinous neoplasms. Immunohistochemistry showed discordant profiles for ovarian (cytokeratin [CK]-7+/paired box 8 [PAX8]+/CK-20-/caudal-type homeobox 2 [CDX-2]-) and appendiceal (CK-20+/CDX-2+/CK-7-/PAX8-) lesions. Peritoneal tumor cells expressed CK-7 but lacked PAX8, CK-20, and CDX-2 expression, supporting an ovarian-type immunophenotype of the peritoneal disease. The patient underwent diagnostic laparoscopy with left salpingo-oophorectomy and removal of the gelatinous ascites. Two cycles of paclitaxel and carboplatin were administered before interval cytoreductive surgery because of advanced disease, arrhythmia, and poor tolerance to prolonged surgery. Complete cytoreduction was achieved through total hysterectomy, right salpingo-oophorectomy, appendectomy, total parietal peritonectomy, omentectomy, cholecystectomy, splenectomy, and the removal of visible disease, followed by carboplatin monotherapy. Complete cytoreduction was achieved, and the patient completed adjuvant carboplatin therapy without grade 3 or higher adverse effects. The patient remained disease-free for 6 months after the completion of chemotherapy.

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Jiyeon Koo

first | Chung-Ang University Hospital | ORCID 0009-0005-3925-642X

Long Ngo Hoang

middle | Chung-Ang University Hospital | ORCID 0000-0001-9787-3462

Mi Kyung Kim

middle | Chung-Ang University Hospital | ORCID 0000-0003-1610-4536

Rae Rim Ryu

middle | Chung-Ang University Hospital | ORCID 0000-0002-2226-4264

Sang Hyun Cho

middle | Chung-Ang University Hospital | ORCID 0000-0001-8289-1190

Gwan Hee Han

middle | Chung-Ang University Hospital | ORCID 0000-0001-5263-4855

Eun‐Ju Lee

last | Chung-Ang University Hospital | ORCID 0000-0001-9446-1059

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BibTeX

@article{Koo2026Pseudomyxoma,
  title = {Pseudomyxoma peritonei from independent primary ovarian and appendiceal tumors: a case report},
  author = {Jiyeon Koo and Long Ngo Hoang and Mi Kyung Kim and Rae Rim Ryu and Sang Hyun Cho and Gwan Hee Han and Eun‐Ju Lee},
  journal = {Journal of Yeungnam Medical Science},
  year = {2026},
  doi = {10.12701/jyms.2026.43.63},
  url = {https://doi.org/10.12701/jyms.2026.43.63}
}

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