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Rare disease
Atypical tumour-like involvement of the colon in secondary systemic amyloidosis which vanished after 1 month of observation
  1. Katuyoshi Ando1,
  2. Mikihiro Fujiya1,
  3. Takahiro Ito1,
  4. Ryuji Sugiyama1,
  5. Toshie Nata1,
  6. Yoshiki Nomura1,
  7. Nobuhiro Ueno1,
  8. Shin Kashima1,
  9. Chisato Ishikawa1,
  10. Yuhiei Inaba1,
  11. Kentaro Moriichi1,
  12. Kotaro Okamoto1,
  13. Katsuya Ikuta1,
  14. Yusuke Mizukami1,
  15. Yoshihiko Tokusashi2,
  16. Naoyuki Miyokawa2,
  17. Jiro Watari3,
  18. Yutaka Kohgo1
  1. 1Division of Gastroenterology and Hematology/Oncology, Department of Medicine, Asahikawa Medical University, Asahikawa, Japan
  2. 2Department of Surgical Pathology, Asahikawa Medical University Hospital, Asahikawa, Japan
  3. 3Division of Upper Gastroenterology, Department of Internal Medicine, Hyogo College of Medicine, Hyogo, Japan
  1. Correspondence to Dr Mikihiro Fujiya, fjym{at}asahikawa-med.ac.jp

Summary

Amyloidosis occurs as a result of the extracellular deposition of protein fibrils in organs and tissues, thus causing mild to severe pathophysiological changes. The gastrointestinal tract is a common site of amyloid deposition. While intestinal amyloidosis frequently results in polypoid lesions, ulcerations, nodules and petechial mucosal haemorrhage, tumour-like lesions are rarely developed and infrequently diagnosed before the resection because of the difficulty in differentiating them from colon cancer. The authors herein reported a case of intestinal amyloid A amyloidosis with a complication of a tumour-like lesion endoscopically resembling a malignant lesion, which was completely diminished after 1 month of observation with bowel rest. Such conservative treatment is a feasible option to cure intestinal tumour-like lesions in patients with intestinal amyloidosis when no neoplastic change is histologically detected, possibly decreasing the need for surgery of the fragile mucosa.

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Footnotes

  • Competing interests None.

  • Patient consent Obtained.