Endobronchial amyloidosis mimicking bronchial asthma: a case report and review of the literature

Author:

Kang Hyun-Wook1,Oh Hyung-Joo1,Park Ha Young1,Park Cheol-Kyu2,Shin Hong-Joon1,Lim Jung-Hwan1,Kwon Yong-Soo1,Oh In-Jae2,Choi Yoo-Duk3

Affiliation:

1. 2Department of Internal Medicine, Chonnam National University Medical School, 671 Jebong-ro, Dong-gu, Gwangju, 501-757, Korea (Republic of)

2. 1Department of Internal Medicine, Chonnam National University Medical School, 671 Jebong-ro, Dong-gu, Gwangju, 501-757, Korea (Republic of), Tel. +82-61-379-7617, Fax +82-61-379-7619

3. 3Department of Pathology, Chonnam National University Medical School, 671 Jebong-ro, Dong-gu, Gwangju, 501-757, Korea (Republic of)

Abstract

AbstractAmong two tracheobronchial forms (local and diffuse) and two parenchymal forms (nodular and alveolar septal) that were reported in previous literature, localized endobronchial amyloidosis is an uncommon disease of unknown cause. Bronchial amyloid deposits can occur as focal nodules or multifocal infiltration of the submucosa. We report the case of a 47-year-old man who had complained of dyspnea and wheezing for 1 month and who had been treated for severe asthma at another hospital. Endobronchial amyloidosis was confirmed by histological examination of the bronchial biopsies.

Publisher

Walter de Gruyter GmbH

Subject

General Medicine

Reference14 articles.

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