Diagnostic Pitfalls in Peritoneal Carcinomatosis: A Case of Pseudomyxoma Peritonei
Pseudomyxoma peritonei (PMP) is a rare pathological condition posing significant diagnostic and management challenges. This article presents a clinical case of a 58-year-old female who was initially diagnosed with stage III primary peritoneal carcinoma. Following neoadjuvant chemotherapy, a diagnostic re-evaluation was performed with histopathological and immunohistochemical review of biopsy specimens, which led to a revised diagnosis of mucinous carcinoma with features consistent with PMP. The patient subsequently underwent complete cytoreductive surgery (CRS) followed by hyperthermic intraperitoneal chemotherapy (HIPEC). She has remained disease-free for 12 months post-operatively. This case illustrates the crucial role of pathological assessment in guiding treatment for PMP and demonstrates favorable long-term outcomes with aggressive CRS and HIPEC in appropriately selected patients.
Authors
- M. Gałka
- Ilya A Tarasau
- Olga P Matylevich (ORCID: https://orcid.org/0000-0003-0732-2101)
- Alena Dalamanava
- Mikalay A. Kurchankou
- Maksim Isachanka (ORCID: https://orcid.org/0009-0004-1727-7994)
- Dmitry Rovski
- S Mavrichev
- Aliaksei M. Kurchankou (ORCID: https://orcid.org/0000-0002-5401-0656)
Institutions
- St. Elizabeth's Medical Center (US)
- N.N. Alexandrov National Cancer Centre (BY)
- Institute of Molecular Genetics (RU)
Publication Details
- Journal
- Cureus
- Published
- 2025-06-06
- DOI
- https://doi.org/10.7759/cureus.85474
- Primary Topic
- Intraperitoneal and Appendiceal Malignancies
- Type
- article
- Field-Weighted Citation Impact
- 0.00