Bronchoscopic Diagnosis and Treatment of Primary Tracheobronchial Amyloidosis: A Retrospective Analysis from China

被引:22
作者
Lu, Xiaoxiao [1 ]
He, Bixiu [1 ]
Wang, Ge [2 ]
He, Baimei [1 ]
Wang, Lijing [1 ]
Chen, Qiong [1 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Geriatr Resp Med, Changsha 410008, Hunan, Peoples R China
[2] Zhengzhou Maternal & Children Hlth Hosp, Dept Informat, Zhengzhou 450012, Henan, Peoples R China
关键词
D O I
10.1155/2017/3425812
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Objective. To assess the value of bronchoscopy in the diagnosis and treatment of primary tracheobronchial amyloidosis (TBA), in order to reduce misdiagnosis rates and improve prognosis. Methods. Clinical data of 107 patients with TBA reported from 1981 to 2015 in China were retrospectively analyzed for clinical features, bronchoscopic manifestations, pathologies, treatments, and outcomes. Results. 105 of 107 TBA patients were pathologically confirmed by bronchoscopy. Main bronchoscopic manifestations of TBA were single or multiple nodules and masses within tracheobronchial lumens; local or diffuse luminal stenosis and obstruction; luminal wall thickening and rigidity; rough or uneven inner luminal walls; congestion and edema of mucosa, which was friable and prone to bleeding upon touch; and so forth. 53 patients were treated with bronchoscopic interventions, like Nd-YAG laser, high-frequency electrotome cautery, freezing, resection, clamping, argon plasma coagulation (APC), microwaving, stent implantation, drug spraying, and other treatments. 51 patients improved, 1 patient worsened, and 1 died. Conclusion. Bronchoscopic biopsy is the primary means of diagnosing TBA. A variety of bronchoscopic interventions have good short-term effects on TBA. Bronchoscopy has important value in the diagnosis, severity assessment, treatment, efficacy evaluation, and prognosis of TBA.
引用
收藏
页数:7
相关论文
共 50 条
[41]   Safety and efficacy of risk-adapted cyclophosphamide, thalidomide, and dexamethasone in systemic AL amyloidosis [J].
Wechalekar, Ashutosh D. ;
Goodman, Hugh J. B. ;
Lachmann, Helen J. ;
Offer, Mark ;
Hawkins, Philip N. ;
Gillmore, Julian D. .
BLOOD, 2007, 109 (02) :457-464
[42]  
Xu L. H., 2013, J NURSING SCI, P36
[43]  
Ying Y. Y., 2014, J SHANDONG U MED EDI, P67
[44]  
Zang S., 1993, HEILONGJIANG MED J, V50
[45]  
Zhang X. N., 1994, HEBEI MED J, V392
[46]  
Zhang Y. H., 2010, INT J RESP, V30, P1161
[47]  
Zhu D. F., 2014, J CLIN PULMONARY MED, P2326
[48]  
何慕芝, 2012, [中华结核和呼吸杂志, Chinese Journal of Tuberculosis and Respiratiory Diseases], V35, P930
[49]  
刘春芳, 2011, [中华结核和呼吸杂志, Chinese Journal of Tuberculosis and Respiratiory Diseases], V34, P479
[50]  
李伟文, 2008, [中华结核和呼吸杂志, Chinese Journal of Tuberculosis and Respiratiory Diseases], V31, P544