Tracheobronchial Amyloidosis: A Rare Airway Disorder With Diagnostic and Therapeutic Challenges—A Case Report and Literature Review

ABSTRACT Tracheobronchial amyloidosis (TBA) is a rare, localised form of amyloidosis characterised by the extracellular deposition of abnormal proteins within the tracheal and bronchial tissues. This condition, although uncommon, can significantly impact airway function, leading to symptoms such as...

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Main Authors: Filip Shterev, Vladimir Aleksiev, Veselin Chonov, Boyko Yavorov, Stanislav Kartev, Dimcho Argirov
Format: Article
Language:English
Published: Wiley 2025-04-01
Series:Respirology Case Reports
Subjects:
Online Access:https://doi.org/10.1002/rcr2.70171
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author Filip Shterev
Vladimir Aleksiev
Veselin Chonov
Boyko Yavorov
Stanislav Kartev
Dimcho Argirov
author_facet Filip Shterev
Vladimir Aleksiev
Veselin Chonov
Boyko Yavorov
Stanislav Kartev
Dimcho Argirov
author_sort Filip Shterev
collection DOAJ
description ABSTRACT Tracheobronchial amyloidosis (TBA) is a rare, localised form of amyloidosis characterised by the extracellular deposition of abnormal proteins within the tracheal and bronchial tissues. This condition, although uncommon, can significantly impact airway function, leading to symptoms such as persistent cough, dyspnea and airway obstruction. This report highlights the clinical presentation, diagnostic approaches and therapeutic options for TBA, emphasising the need for individualised management strategies and comprehensive patient care. This case describes a 62‐year‐old male with a history of smoking debuting with progressive hoarseness, dyspnea and dysphagia, who was initially diagnosed with tracheobronchial amyloidosis following biopsy of a subglottic mass. After surgical excision and a 3‐year disease‐free interval, he experienced multiple recurrences requiring further interventions, including bronchoscopic evaluation. Histopathological confirmation of recurrent amyloidosis led to a decision for strict follow‐up, as symptoms remained mild post‐biopsy.
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spelling doaj-art-1ecdc7ed0b2f44c3958d9c8bacfa60962025-08-20T02:29:29ZengWileyRespirology Case Reports2051-33802025-04-01134n/an/a10.1002/rcr2.70171Tracheobronchial Amyloidosis: A Rare Airway Disorder With Diagnostic and Therapeutic Challenges—A Case Report and Literature ReviewFilip Shterev0Vladimir Aleksiev1Veselin Chonov2Boyko Yavorov3Stanislav Kartev4Dimcho Argirov5I‐st Department of Internal Diseases, Section of Pneumology and Phthysiatrics Medical University of Plovdiv Plovdiv BulgariaClinic of Thoracic Surgery Plovdiv University Multiprofile Hospital for Active Treatment Kaspela Plovdiv BulgariaDepartment of Clinical Pathology Plovdiv University Multiprofile Hospital for Active Treatment Kaspela Plovdiv BulgariaClinic of Thoracic Surgery Plovdiv University Multiprofile Hospital for Active Treatment Kaspela Plovdiv BulgariaI‐st Department of Internal Diseases, Section of Pneumology and Phthysiatrics Medical University of Plovdiv Plovdiv BulgariaClinic of Thoracic Surgery Plovdiv University Multiprofile Hospital for Active Treatment Kaspela Plovdiv BulgariaABSTRACT Tracheobronchial amyloidosis (TBA) is a rare, localised form of amyloidosis characterised by the extracellular deposition of abnormal proteins within the tracheal and bronchial tissues. This condition, although uncommon, can significantly impact airway function, leading to symptoms such as persistent cough, dyspnea and airway obstruction. This report highlights the clinical presentation, diagnostic approaches and therapeutic options for TBA, emphasising the need for individualised management strategies and comprehensive patient care. This case describes a 62‐year‐old male with a history of smoking debuting with progressive hoarseness, dyspnea and dysphagia, who was initially diagnosed with tracheobronchial amyloidosis following biopsy of a subglottic mass. After surgical excision and a 3‐year disease‐free interval, he experienced multiple recurrences requiring further interventions, including bronchoscopic evaluation. Histopathological confirmation of recurrent amyloidosis led to a decision for strict follow‐up, as symptoms remained mild post‐biopsy.https://doi.org/10.1002/rcr2.70171airway obstructionbronchoscopyprotein depositiontherapeutic managementtracheobronchial amyloidosis
spellingShingle Filip Shterev
Vladimir Aleksiev
Veselin Chonov
Boyko Yavorov
Stanislav Kartev
Dimcho Argirov
Tracheobronchial Amyloidosis: A Rare Airway Disorder With Diagnostic and Therapeutic Challenges—A Case Report and Literature Review
Respirology Case Reports
airway obstruction
bronchoscopy
protein deposition
therapeutic management
tracheobronchial amyloidosis
title Tracheobronchial Amyloidosis: A Rare Airway Disorder With Diagnostic and Therapeutic Challenges—A Case Report and Literature Review
title_full Tracheobronchial Amyloidosis: A Rare Airway Disorder With Diagnostic and Therapeutic Challenges—A Case Report and Literature Review
title_fullStr Tracheobronchial Amyloidosis: A Rare Airway Disorder With Diagnostic and Therapeutic Challenges—A Case Report and Literature Review
title_full_unstemmed Tracheobronchial Amyloidosis: A Rare Airway Disorder With Diagnostic and Therapeutic Challenges—A Case Report and Literature Review
title_short Tracheobronchial Amyloidosis: A Rare Airway Disorder With Diagnostic and Therapeutic Challenges—A Case Report and Literature Review
title_sort tracheobronchial amyloidosis a rare airway disorder with diagnostic and therapeutic challenges a case report and literature review
topic airway obstruction
bronchoscopy
protein deposition
therapeutic management
tracheobronchial amyloidosis
url https://doi.org/10.1002/rcr2.70171
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