Successful treatment of pseudomyxoma peritonei (PMP) through cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (CRS-HIPEC): A case report and literature review

Pseudomyxoma peritonei (PMP) is characterized by the accumulation of mucinous fluid in the abdominal cavity, typically originating from mucin-producing tumors, most commonly arising in the appendix. A 63-year-old male patient presented to the hospital with complaints of abdominal pain, significant w...

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Veröffentlicht in:International journal of surgery case reports 2024-06, Vol.119, p.109656, Article 109656
Hauptverfasser: Awad, Areej, Awad, Mahmoud, Alami, Muayyad, Sablan, Aseel Abu, Shrateh, Oadi N., Jubran, Fahmi
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Sprache:eng
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Zusammenfassung:Pseudomyxoma peritonei (PMP) is characterized by the accumulation of mucinous fluid in the abdominal cavity, typically originating from mucin-producing tumors, most commonly arising in the appendix. A 63-year-old male patient presented to the hospital with complaints of abdominal pain, significant weight loss, a palpable mass in the right iliac fossa, and evidence of ascites. A diagnosis of PMP was proposed based on findings from a computed tomography (CT) scan, which was subsequently confirmed through histopathological examination of a biopsy. The patient underwent successful treatment with Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy (CRS-HIPEC). Diagnosing PMP presents challenges due to its rarity and the potential for extensive spread throughout the peritoneal cavity, necessitating a multidisciplinary approach for successful treatment. Pseudomyxoma peritonei is a rare yet medically significant condition. Documenting a case of this ailment in Palestine has the potential to advance medical understanding, raise awareness, and improve patient care standards within the local healthcare system. By documenting this uncommon condition, healthcare practitioners in Palestine can gain valuable insights into its manifestations, diagnostic processes, and treatment modalities. This contribution not only enriches the global medical literature but also promotes collaboration in addressing the challenges associated with rare diseases. •Pseudomyxoma peritonei (PMP) is characterized by mucinous fluid accumulation in the abdomen, typically originating from mucin-producing tumors, primarily found in the appendix.•PMP diagnosis poses challenges due to its rarity and potential for peritoneal spread, highlighting the necessity for a multidisciplinary treatment approach.•Documenting this PMP case in Palestine contributes to medical knowledge, enhances local healthcare, and emphasizes the importance of collaborative efforts in managing rare diseases.
ISSN:2210-2612
2210-2612
DOI:10.1016/j.ijscr.2024.109656