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Rare tumours of the appendix that range from slow mucin-producing growths that fill the abdomen (pseudomyxoma peritonei) to aggressive adenocarcinomas. The slow forms are treated by extensive surgery with heated chemotherapy in the abdomen; the fast ones like colon cancer.
Appendiceal neoplasms include low-grade appendiceal mucinous neoplasms (LAMN) that rupture and seed the peritoneum as pseudomyxoma peritonei (PMP), mucinous and non-mucinous adenocarcinomas, goblet cell adenocarcinoma, and neuroendocrine tumours (the most common appendix tumour, usually cured by appendicectomy). PSOGI grading (acellular mucin, low-grade, high-grade, signet ring) predicts outcome. GNAS mutations mark low-grade mucinous disease; KRAS, TP53 and SMAD4 mark higher grade.
For PMP and peritoneal disease, cytoreductive surgery (CRS) with hyperthermic intraperitoneal chemotherapy (HIPEC, usually mitomycin C) at an experienced centre gives 10-year survival of ~60-70% for low-grade disease (Sugarbaker, Chua 2012). Systemic chemotherapy (FOLFOX/CAPOX) is used for high-grade and unresectable disease but a randomised trial (2024) showed no benefit in low-grade mucinous carcinoma peritonei. Iterative CRS, mucolytics (bromelain-acetylcysteine) and intraperitoneal therapies are under study. Appendiceal adenocarcinoma is otherwise managed like colorectal cancer, with right hemicolectomy and stage-based chemotherapy.
| Setting | Approach | Guideline |
|---|---|---|
| Localised LAMN / adenocarcinoma | Appendicectomy (LAMN without perforation) or right hemicolectomy (adenocarcinoma, goblet cell); adjuvant chemotherapy for node-positive adenocarcinoma by colorectal analogy. | NCCN Category 2A |
| Pseudomyxoma peritonei / peritoneal disease | Cytoreductive surgery with HIPEC at a peritoneal-surface-malignancy centre; repeat CRS for recurrence when feasible. | not mapped |
| High-grade or unresectable peritoneal disease | FOLFOX/CAPOX ± bevacizumab; systemic chemotherapy has no proven benefit in low-grade disease (randomised 2024). | not mapped |