Orphan Lung Diseases

被引:3
|
作者
Ali, Muhammad Sajawal [1 ]
Ghori, Uzair Khan [1 ]
Musani, Ali, I [2 ]
机构
[1] Med Coll Wisconsin, Div Pulm & Crit Care Med, HUB Collaborat Med, 8701 West Watertown Plank Rd, Milwaukee, WI 53226 USA
[2] Univ Colorado, Div Pulm Sci & Crit Care Med, Acad Off 1,12631 East 17th Ave,M-S C323,Off 8102, Aurora, CO 80045 USA
关键词
Orphan lung diseases; Rare lung diseases; Pleuroparenchymal fibroelastosis; Pulmonary alveolar proteinosis; Lymphangioleiomyomatosis; Yellow nail syndrome; Mounier-Kuhn syndrome; PULMONARY ALVEOLAR PROTEINOSIS; YELLOW NAIL SYNDROME; IDIOPATHIC PLEUROPARENCHYMAL FIBROELASTOSIS; MOUNIER-KUHN-SYNDROME; CLINICAL-FEATURES; CT FEATURES; LYMPHANGIOLEIOMYOMATOSIS; DIAGNOSIS; CLASSIFICATION; GUIDELINES;
D O I
10.1016/j.mcna.2018.12.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There are hundreds of rare orphan lung diseases. We have highlighted five of them, one from each of the five major categories of pulmonary disorders: pleuroparenchymal fibroelastosis (a rare diffuse parenchymal lung disease), pulmonary alveolar proteinosis (a rare autoimmune and diffuse parenchymal lung disease), lymphangioleiomyomatosis (a rare cystic lung disease), yellow nail syndrome (a rare pleural disease), and Mounier-Kuhn syndrome (a rare airway disorder). The pathogenesis, clinical presentation, diagnostic criteria, treatment options, and prognosis of each disorder is discussed. This review is by no means exhaustive and further research is needed to improve our understanding of these disorders.
引用
收藏
页码:503 / +
页数:14
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