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 language | English |
|---|---|
| Pages (from-to) | 79-82 |
| Number of pages | 4 |
| Journal | Chinese Journal of Radiology (Taiwan) |
| Volume | 25 |
| Issue number | 2 |
| State | Published - 2000 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- Amyloidosis
- Bronchi, CT
- Larynx, CT
- Trachea, CT
Fingerprint
Dive into the research topics of 'Laryngotracheobronchial amyloidosis: A case report and review of articles'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver