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本文引用的文献

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Amyloidosis: a clinical overview.淀粉样变性:临床概述。
Rheum Dis Clin North Am. 2013 May;39(2):323-45. doi: 10.1016/j.rdc.2013.02.012. Epub 2013 Mar 13.
2
Outcome of AL amyloidosis after high-dose melphalan and autologous stem cell transplantation: long-term results in a series of 421 patients.大剂量美法仑和自体干细胞移植后 AL 淀粉样变性的结果:一系列 421 例患者的长期结果。
Blood. 2011 Oct 20;118(16):4346-52. doi: 10.1182/blood-2011-01-330738. Epub 2011 Aug 9.
3
Aging and transthyretin-related amyloidosis: pathologic examinations in pulmonary amyloidosis.衰老与转甲状腺素蛋白相关淀粉样变性:肺淀粉样变性的病理检查
Amyloid. 2006 Mar;13(1):24-30. doi: 10.1080/13506120500537194.
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Interpretative strategies for lung function tests.肺功能测试的解读策略。
Eur Respir J. 2005 Nov;26(5):948-68. doi: 10.1183/09031936.05.00035205.
5
Standardisation of the single-breath determination of carbon monoxide uptake in the lung.肺一氧化碳摄取单次呼吸测定的标准化
Eur Respir J. 2005 Oct;26(4):720-35. doi: 10.1183/09031936.05.00034905.
6
Pulmonary and tracheobronchial amyloidosis.肺及气管支气管淀粉样变性
Semin Respir Crit Care Med. 2002 Apr;23(2):155-65. doi: 10.1055/s-2002-25304.
7
Standardisation of spirometry.肺活量测定法的标准化
Eur Respir J. 2005 Aug;26(2):319-38. doi: 10.1183/09031936.05.00034805.
8
Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis, Tours, France, 18-22 April 2004.免疫球蛋白轻链淀粉样变性(AL)中器官受累及治疗反应的定义:2004年4月18 - 22日于法国图尔举行的第10届国际淀粉样变性和淀粉样变研讨会的共识意见
Am J Hematol. 2005 Aug;79(4):319-28. doi: 10.1002/ajh.20381.
9
Transthyretin-derived senile systemic amyloidosis: clinicopathologic and structural considerations.转甲状腺素蛋白源性老年系统性淀粉样变性:临床病理及结构考量
Amyloid. 2003 Aug;10 Suppl 1:48-54.
10
A rapid plethysmographic method for measuring thoracic gas volume: a comparison with a nitrogen washout method for measuring functional residual capacity in normal subjects.一种测量胸内气体容积的快速体积描记法:与氮洗出法测量正常受试者功能残气量的比较
J Clin Invest. 1956 Mar;35(3):322-6. doi: 10.1172/JCI103281.

经支气管活检可安全诊断淀粉样肺病。

Transbronchial biopsies safely diagnose amyloid lung disease.

作者信息

Govender Praveen, Keyes Colleen M, Hankinson Elizabeth A, O'Hara Carl J, Sanchorawala Vaishali, Berk John L

机构信息

a Pulmonary Center, Boston Medical Center , Boston , MA , USA.

b Department of Medicine , Boston Medical Center , Boston , MA , USA.

出版信息

Amyloid. 2017 Mar;24(1):37-41. doi: 10.1080/13506129.2017.1301917. Epub 2017 Apr 10.

DOI:10.1080/13506129.2017.1301917
PMID:28393574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6014610/
Abstract

BACKGROUND

Autopsy identifies lung involvement in 58-92% of patients with the most prevalent forms of systemic amyloidoses. In the absence of lung biopsies, amyloid lung disease often goes unrecognized. Report of a death following transbronchial biopsies in a patient with systemic amyloidosis cautioned against the procedure in this patient cohort. We reviewed our experience with transbronchial biopsies in patients with amyloidosis to determine the safety and utility of bronchoscopic lung biopsies.

METHODS

We identified patients referred to the Amyloidosis Center at Boston Medical Center with lung amyloidosis diagnosed by transbronchial lung biopsies (TBBX). Amyloid typing was determined by immunohistochemistry or mass spectrometry. Standard end organ assessments, including pulmonary function test (PFT) and chest tomography (CT) imaging, and extra-thoracic biopsies established the extent of disease.

RESULTS

Twenty-five (21.7%) of 115 patients with lung amyloidosis were diagnosed by TBBX. PFT classified 33.3% with restrictive physiology, 28.6% with obstructive disease, and 9.5% mixed physiology; 9.5% exhibited isolated diffusion defects while 19% had normal pulmonary testing. Two view chest or CT imaging identified focal opacities in 52% of cases and diffuse interstitial disease in 48%. Amyloid type and disease extent included 68% systemic AL disease, 16% localized (lung limited) AL disease, 12% ATTR disease, and 4% AA amyloidosis. Fluoroscopy was not used during biopsy. No procedure complications were reported.

CONCLUSIONS

Our case series of 25 patients supports the use of bronchoscopic transbronchial biopsies for diagnosis of parenchymal lung amyloidosis. Normal PFTs do not rule out the histologic presence of amyloid lung disease.

摘要

背景

尸检发现,在最常见的几种系统性淀粉样变性患者中,58% - 92%存在肺部受累情况。在没有进行肺活检的情况下,淀粉样肺病常常未被识别。有报告称,一名系统性淀粉样变性患者在经支气管活检后死亡,这警示了在该患者群体中进行此项操作时需谨慎。我们回顾了我们在淀粉样变性患者中进行经支气管活检的经验,以确定支气管镜肺活检的安全性和实用性。

方法

我们确定了转诊至波士顿医疗中心淀粉样变性中心、经支气管肺活检(TBBX)诊断为肺淀粉样变性的患者。通过免疫组织化学或质谱法进行淀粉样蛋白分型。包括肺功能测试(PFT)和胸部断层扫描(CT)成像在内的标准终末器官评估以及胸外活检确定了疾病的范围。

结果

115例肺淀粉样变性患者中有25例(21.7%)通过TBBX确诊。PFT将33.3%的患者归类为限制性生理功能障碍,28.6%为阻塞性疾病,9.5%为混合性生理功能障碍;9.5%表现为单纯弥散功能缺陷,而19%的患者肺功能测试正常。双视图胸部X线或CT成像在52%的病例中发现局灶性混浊,48%发现弥漫性间质性疾病。淀粉样蛋白类型和疾病范围包括68%的系统性AL疾病、16%的局限性(肺局限性)AL疾病、12%的ATTR疾病和4%的AA淀粉样变性。活检过程中未使用荧光镜检查。未报告任何操作并发症。

结论

我们的25例病例系列支持使用支气管镜经支气管活检来诊断实质性肺淀粉样变性。正常的PFT结果并不能排除淀粉样肺病的组织学存在。