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March 25, 2026ACG Case Reports Journal0 citationsOpen Access

Rare Rectal Involvement of Metastatic Appendiceal Adenocarcinoma Mimicking Primary Rectal Cancer

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NANesrine AboulhamidAZA ZoughlamiGEGertruda Evaristo

Key Points

  • This case aims to highlight the rare occurrence of rectal metastasis from appendiceal adenocarcinoma and explore potential mechanisms for this phenomenon.
  • Described a case of a 44-year-old man with metastatic appendiceal adenocarcinoma.
  • Evaluated symptoms including constipation and tenesmus following prior cancer treatment.
  • Performed colonoscopy and histological analysis to assess the nature of the rectal mass.
  • Identified a large ulcerated mass in the rectum consistent with metastatic appendiceal adenocarcinoma.
  • Histological findings showed poorly differentiated adenocarcinoma with specific immunoprofile markers.
  • This case represents one of only two documented instances of rectal metastasis from appendiceal cancer.

Abstract

Abstract Primary appendiceal adenocarcinoma is a rare gastrointestinal malignancy that typically metastasizes to the peritoneum. Metastatic rectal involvement is exceptionally rare. We describe the case of a previously healthy 44-year-old man diagnosed with metastatic appendiceal adenocarcinoma. Sixteen months after cytoreductive surgery and hyperthermic intraperitoneal chemotherapy, he developed new-onset constipation and tenesmus. Subsequent colonoscopy revealed a large ulcerated rectal mass, consistent with possible metastatic poorly differentiated adenocarcinoma based on histology, immunoprofiling (CK20-positive, CDX2-positive, CK7-negative), and clinical history. To our knowledge, this represents the second possible documented case of rectal metastasis from appendiceal cancer in the literature, and the first to propose a potential mechanism for its spread.

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Cite This Study

Aboulhamid et al. (2026) studied this question.

synapsesocial.com/papers/69c37bf3b34aaaeb1a67ecb4https://doi.org/10.14309/crj.0000000000002045
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