Cargando…
Laryngotracheobronchial amyloidosis: A case report
Primary laryngotracheobronchial amyloidosis is a rare pulmonary disease that can cause endobronchial stenosis. This disease has never previously been reported in Vietnam. We aimed to report a laryngotracheobronchial amyloidosis case in a 43-year-old female, which may be the first reported case in Vi...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7972980/ https://www.ncbi.nlm.nih.gov/pubmed/33747762 http://dx.doi.org/10.1016/j.rmcr.2021.101377 |
_version_ | 1783666750324211712 |
---|---|
author | Thuong Vu, Le Minh Duc, Nguyen Tra My, Thieu-Thi Ba Tung, Nguyen Phuong Thuy, Le Tu Minh Thong, Pham |
author_facet | Thuong Vu, Le Minh Duc, Nguyen Tra My, Thieu-Thi Ba Tung, Nguyen Phuong Thuy, Le Tu Minh Thong, Pham |
author_sort | Thuong Vu, Le |
collection | PubMed |
description | Primary laryngotracheobronchial amyloidosis is a rare pulmonary disease that can cause endobronchial stenosis. This disease has never previously been reported in Vietnam. We aimed to report a laryngotracheobronchial amyloidosis case in a 43-year-old female, which may be the first reported case in Vietnam. The patient had a 4-year history of progressive hoarseness, dyspnea, and hemoptysis. Multiple bronchial biopsies combined with detailed clinical information suggested an amyloidosis disease. Red congo staining was positive in bronchial samples, and a further workup found positive red congo staining in subcutaneous fatty tissue biopsy samples. Tracheostomy was performed due to severe dyspnea related to laryngeal stenosis. A multidisciplinary consultation was held, and chemotherapy with melphalan and dexamethasone were prescribed due to the systemic effects of the disease. After 2 cycles of chemotherapy, the patient showed improvement in dyspnea and cough. Due to the inexperience of both the clinicians and pathologists, this case was diagnosed quite late. In the future, if this diagnosis is considered in the differential diagnosis, an earlier diagnosis and better treatment outcome can be reached. |
format | Online Article Text |
id | pubmed-7972980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-79729802021-03-19 Laryngotracheobronchial amyloidosis: A case report Thuong Vu, Le Minh Duc, Nguyen Tra My, Thieu-Thi Ba Tung, Nguyen Phuong Thuy, Le Tu Minh Thong, Pham Respir Med Case Rep Case Report Primary laryngotracheobronchial amyloidosis is a rare pulmonary disease that can cause endobronchial stenosis. This disease has never previously been reported in Vietnam. We aimed to report a laryngotracheobronchial amyloidosis case in a 43-year-old female, which may be the first reported case in Vietnam. The patient had a 4-year history of progressive hoarseness, dyspnea, and hemoptysis. Multiple bronchial biopsies combined with detailed clinical information suggested an amyloidosis disease. Red congo staining was positive in bronchial samples, and a further workup found positive red congo staining in subcutaneous fatty tissue biopsy samples. Tracheostomy was performed due to severe dyspnea related to laryngeal stenosis. A multidisciplinary consultation was held, and chemotherapy with melphalan and dexamethasone were prescribed due to the systemic effects of the disease. After 2 cycles of chemotherapy, the patient showed improvement in dyspnea and cough. Due to the inexperience of both the clinicians and pathologists, this case was diagnosed quite late. In the future, if this diagnosis is considered in the differential diagnosis, an earlier diagnosis and better treatment outcome can be reached. Elsevier 2021-03-04 /pmc/articles/PMC7972980/ /pubmed/33747762 http://dx.doi.org/10.1016/j.rmcr.2021.101377 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Thuong Vu, Le Minh Duc, Nguyen Tra My, Thieu-Thi Ba Tung, Nguyen Phuong Thuy, Le Tu Minh Thong, Pham Laryngotracheobronchial amyloidosis: A case report |
title | Laryngotracheobronchial amyloidosis: A case report |
title_full | Laryngotracheobronchial amyloidosis: A case report |
title_fullStr | Laryngotracheobronchial amyloidosis: A case report |
title_full_unstemmed | Laryngotracheobronchial amyloidosis: A case report |
title_short | Laryngotracheobronchial amyloidosis: A case report |
title_sort | laryngotracheobronchial amyloidosis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7972980/ https://www.ncbi.nlm.nih.gov/pubmed/33747762 http://dx.doi.org/10.1016/j.rmcr.2021.101377 |
work_keys_str_mv | AT thuongvule laryngotracheobronchialamyloidosisacasereport AT minhducnguyen laryngotracheobronchialamyloidosisacasereport AT tramythieuthi laryngotracheobronchialamyloidosisacasereport AT batungnguyen laryngotracheobronchialamyloidosisacasereport AT phuongthuyletu laryngotracheobronchialamyloidosisacasereport AT minhthongpham laryngotracheobronchialamyloidosisacasereport |