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

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

^*此作品的通信作者

醫學影像暨放射科學系(含學碩博士班)

Chang Gung Memorial Hospital

研究成果: 期刊稿件 › 文章 › 同行評審

摘要

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.

原文	英語
頁（從 - 到）	79-82
頁數	4
期刊	Chinese Journal of Radiology
卷	25
發行號	2
出版狀態	已出版 - 2000

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title = "Laryngotracheobronchial amyloidosis: A case report and review of articles",

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.",

keywords = "Amyloidosis, Bronchi, CT, Larynx, CT, Trachea, CT",

author = "Chen, {Y. L.} and Cheung, {Y. C.} and Lee, {K. F.} and Wong, {H. F.} and Lu, {K. W.} and Ng, {S. H.} and Yau-Yau Wai and Wan, {Y. L.}",

year = "2000",

language = "英语",

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T1 - Laryngotracheobronchial amyloidosis

T2 - A case report and review of articles

AU - Chen, Y. L.

AU - Cheung, Y. C.

AU - Lee, K. F.

AU - Wong, H. F.

AU - Lu, K. W.

AU - Ng, S. H.

AU - Wai, Yau-Yau

AU - Wan, Y. L.

PY - 2000

Y1 - 2000

N2 - 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.

AB - 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.

KW - Amyloidosis

KW - Bronchi, CT

KW - Larynx, CT

KW - Trachea, CT

UR - http://www.scopus.com/inward/record.url?scp=0033780429&partnerID=8YFLogxK

M3 - 文章

AN - SCOPUS:0033780429

SN - 1018-8940

VL - 25

SP - 79

EP - 82

JO - Chinese Journal of Radiology

JF - Chinese Journal of Radiology

IS - 2

ER -

Laryngotracheobronchial amyloidosis: A case report and review of articles

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