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Laryngotracheobronchial amyloidosis: A case report and review of articles

  • Y. L. Chen*
  • , Y. C. Cheung
  • , K. F. Lee
  • , H. F. Wong
  • , K. W. Lu
  • , S. H. Ng
  • , Yau-Yau Wai
  • , Y. L. Wan
  • *Corresponding author for this work
  • Chang Gung Memorial Hospital

Research output: Contribution to journalJournal Article peer-review

Abstract

Amyloidosis is a rare disease caused by extracellular deposition of an insoluble protein. We report a 74-year-old male with histologically proven laryngotracheobronchial amyloidosis. He presented with stridor, dyspnea and repeated pneumonia for many years. Thoracic computed tomography (CT) disclosed diffuse thickening and nodularity with calcified spots over the larynx and tracheobronchial trees. It was suggestive of localized pulmonary amyloidosis.

Original languageEnglish
Pages (from-to)79-82
Number of pages4
JournalChinese Journal of Radiology (Taiwan)
Volume25
Issue number2
StatePublished - 2000

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Amyloidosis
  • Bronchi, CT
  • Larynx, CT
  • Trachea, CT

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