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呼吸系统淀粉样变:16例最初由肺科医生诊断出的淀粉样变患者。

Amyloidosis of the respiratory system: 16 patients with amyloidosis initially diagnosed by pulmonologists.

作者信息

Yamada Masami, Takayanagi Noboru, Yamakawa Hideaki, Ishiguro Takashi, Baba Tomohisa, Shimizu Yoshihiko, Okudela Koji, Takemura Tamiko, Ogura Takashi

机构信息

Dept of Respiratory Medicine, Saitama Cardiovascular and Respiratory Center, Saitama, Japan.

Dept of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, Yokohama, Japan.

出版信息

ERJ Open Res. 2020 Jul 27;6(3). doi: 10.1183/23120541.00313-2019. eCollection 2020 Jul.

Abstract

BACKGROUND

diagnosis of amyloidosis of the respiratory system is rare. Few data are available regarding clinical presentation, precursor proteins, diagnostic procedures, comorbidities, complications, and outcome. We assessed clinical features of a series of patients with amyloidosis of the respiratory system in two Japanese centres.

METHODS

Medical records of 16 patients with amyloidosis of the respiratory system were retrospectively analysed. Amyloid was diagnosed by polarisation microscopy using Congo red-stained tissue specimens and classified immunohistochemically.

RESULTS

Median patient age was 71 years, and median follow-up period was 5 years. Immunoglobulin light-chain (AL)-λ amyloidosis was found in eight and AL-κ in five patients. Two patients harboured wild-type transthyretin and one harboured serum amyloid A-derived amyloid. Five different forms of amyloidosis of the respiratory system were observed: nodular pulmonary amyloidosis (seven patients), diffuse alveolar-septal amyloidosis (five), mediastinal lymph node amyloidosis (three), tracheobronchial amyloidosis (one), and pleural amyloidosis (one). One patient had diffuse alveolar-septal amyloidosis and mediastinal lymph node amyloidosis. Three of five patients with diffuse alveolar-septal amyloidosis were diagnosed by transbronchial lung biopsy as having concurrent diffuse alveolar haemorrhage or pneumocystis pneumonia. Two of three patients with mediastinal lymph node amyloidosis were diagnosed by endobronchial ultrasound-guided transbronchial needle aspiration.

CONCLUSIONS

Not only nodular pulmonary amyloidosis, diffuse alveolar-septal amyloidosis, and tracheobronchial amyloidosis but also mediastinal lymph node amyloidosis and pleural amyloidosis should be considered in the differential diagnosis of amyloidosis of the respiratory system. Useful diagnostic methods include transbronchial lung biopsy for diffuse alveolar-septal amyloidosis and endobronchial ultrasound-guided transbronchial needle aspiration for mediastinal lymph node amyloidosis.

摘要

背景

呼吸系统淀粉样变性的诊断较为罕见。关于临床表现、前体蛋白、诊断程序、合并症、并发症及预后的数据较少。我们评估了日本两个中心一系列呼吸系统淀粉样变性患者的临床特征。

方法

对16例呼吸系统淀粉样变性患者的病历进行回顾性分析。通过对刚果红染色的组织标本进行偏振显微镜检查诊断淀粉样变性,并进行免疫组织化学分类。

结果

患者中位年龄为71岁,中位随访期为5年。8例患者为免疫球蛋白轻链(AL)-λ淀粉样变性,5例为AL-κ淀粉样变性。2例患者为野生型转甲状腺素蛋白淀粉样变性,1例为血清淀粉样蛋白A衍生的淀粉样变性。观察到呼吸系统淀粉样变性的五种不同形式:结节性肺淀粉样变性(7例)、弥漫性肺泡间隔淀粉样变性(5例)、纵隔淋巴结淀粉样变性(3例)、气管支气管淀粉样变性(1例)和胸膜淀粉样变性(1例)。1例患者同时患有弥漫性肺泡间隔淀粉样变性和纵隔淋巴结淀粉样变性。5例弥漫性肺泡间隔淀粉样变性患者中有3例经支气管肺活检诊断并发弥漫性肺泡出血或肺孢子菌肺炎。3例纵隔淋巴结淀粉样变性患者中有2例经支气管内超声引导下经支气管针吸活检确诊。

结论

在呼吸系统淀粉样变性的鉴别诊断中,不仅应考虑结节性肺淀粉样变性、弥漫性肺泡间隔淀粉样变性和气管支气管淀粉样变性,还应考虑纵隔淋巴结淀粉样变性和胸膜淀粉样变性。有用的诊断方法包括用于弥漫性肺泡间隔淀粉样变性的经支气管肺活检和用于纵隔淋巴结淀粉样变性的支气管内超声引导下经支气管针吸活检。

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