Govender Praveen, Keyes Colleen M, Hankinson Elizabeth A, O'Hara Carl J, Sanchorawala Vaishali, Berk John L
a Pulmonary Center, Boston Medical Center , Boston , MA , USA.
b Department of Medicine , Boston Medical Center , Boston , MA , USA.
Amyloid. 2017 Mar;24(1):37-41. doi: 10.1080/13506129.2017.1301917. Epub 2017 Apr 10.
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.
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.
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.
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.
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。
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。
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。
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。