异体造血干细胞移植后出现气管支气管畸形。

IF 0.8 Q4 RESPIRATORY SYSTEM Respirology Case Reports Pub Date : 2024-04-30 eCollection Date: 2024-05-01 DOI:10.1002/rcr2.1348
Pitirat Panpruang, Dararat Eksombatchai, Viboon Boonsarngsuk
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引用次数: 0

摘要

气管支气管软化症(TBM)是由于气管软骨部分变弱,导致气道功能受损,引起呼吸困难、咳嗽和无法清除分泌物等症状。支气管炎闭塞综合征(BOS)是异基因造血干细胞移植(HSCT)患者最常见的晚期非感染性肺部并发症。因此,异基因造血干细胞移植后出现进行性呼吸困难和慢性咳嗽、肺功能测试出现新的阻塞模式的患者,通常被诊断为移植后BOS。但需要注意的是,TBM 也可在肺功能检查中表现为阻塞性缺损模式。据报道,气管瘘是异基因干细胞移植的罕见并发症。我们介绍了两名在异基因造血干细胞移植后出现气管瘘的患者,他们最初接受了移植后BOS治疗,但症状并未改善。然而,经过持续气道正压治疗后,他们的症状有所缓解。
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Tracheobronchomalacia following allogeneic haematopoietic stem cell transplantation.

Tracheobronchomalacia (TBM) occurs due to the weakening of cartilaginous part of the trachea, resulting in compromised airway function and leading to symptoms such as dyspnea, cough, and inability to clear secretions. Bronchiolitis obliterans syndrome (BOS) is the most prevalent late noninfectious pulmonary complication in patients who underwent allogeneic haematopoietic stem cell transplantation (HSCT). Therefore, patients experiencing progressive dyspnea and chronic cough after allogenic HSCT, with new obstructive pattern on pulmonary function test, are typically diagnosed with post-transplant BOS. However, it is important to note that TBM can also manifest as an obstructive defect pattern on pulmonary function test. Tracheomalacia has been reported as a rare complication of allogenic stem cell transplantation. We present two patients who developed TBM following allogeneic HSCT and were initially treated for post-transplant BOS but did not experience symptom improvement. However, after treatment with continuous positive airway pressure, their symptom subsided.

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来源期刊
Respirology Case Reports
Respirology Case Reports RESPIRATORY SYSTEM-
CiteScore
1.40
自引率
0.00%
发文量
178
审稿时长
8 weeks
期刊介绍: Respirology Case Reports is an open-access online journal dedicated to the publication of original clinical case reports, case series, clinical images and clinical videos in all fields of respiratory medicine. The Journal encourages the international exchange between clinicians and researchers of experiences in diagnosing and treating uncommon diseases or diseases with unusual presentations. All manuscripts are peer-reviewed through a streamlined process that aims at providing a rapid turnaround time from submission to publication.
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