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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
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Classification of cystic lung disease in adults

Classification of cystic lung disease in adults
Classification Description
  1. Neoplastic
  • Lymphangioleiomyomatosis – sporadic as well as associated with tuberous sclerosis
  • Pulmonary Langerhans cell histiocytosis and non-Langerhans cell histiocytoses, including Erdheim-Chester disease
  • Other primary and metastatic neoplasms, such as sarcomas, adenocarcinomas, pleuropulmonary blastoma, etc
  1. Genetic/developmental/congenital
  • Birt-Hogg-Dubé syndrome
  • Proteus syndrome, neurofibromatosis, Ehlers-Danlos syndrome
  • Congenital pulmonary airway malformation, bronchopulmonary dysplasia, etc
  1. Associated with lymphoproliferative and connective tissue disorders
  • Lymphocytic interstitial pneumonia
  • Follicular bronchiolitis
  • Sjögren's disease
  • Amyloidosis
  • Light-chain deposition disease
  1. Infectious
  • Pneumocystis jiroveci
  • Staphylococcal pneumonia
  • Recurrent respiratory papillomatosis
  • Endemic fungal diseases, especially coccidioidomycosis
  • Paragonimiasis
  1. Associated with interstitial lung diseases
  • Hypersensitivity pneumonitis
  • Desquamative interstitial pneumonia
  1. Smoking related
  • Pulmonary Langerhans cell histiocytosis
  • Desquamative interstitial pneumonia
  • Respiratory bronchiolitis
  1. Other/miscellaneous
  • Post-traumatic pseudocysts
  • Fire-eater's lung
  • Hyper-IgE syndrome
  1. DCLD mimics
  • Emphysema
  • Alpha-1 antitrypsin deficiency
  • Bronchiectasis
  • Honeycombing seen in late-stage scarring interstitial lung diseases
Many DCLDs have overlapping features and can be classified in more than one category. Pulmonary Langerhans cell histiocytosis is classified as both a neoplasm and a smoking-related cystic lung disease. Similarly, desquamative interstitial pneumonia is an interstitial lung disease as well as a smoking-related cystic lung disease. Although classified as a lymphoproliferative disorder, light-chain deposition disease could also be considered under the neoplastic category. Similarly, hyper-IgE syndrome, although classified as other/miscellaneous, could also be classified under the category of infections causing cystic lung disease.
DCLD: diffuse cystic lung disease.
Reprinted with permission of the American Thoracic Society. Copyright © 2015 American Thoracic Society. Gupta N, Vassallo R, Wikenheiser-Brokamp KA, McCormack FX. Diffuse Cystic Lung Disease. Part I. Am J Respir Crit Care Med 2015; 191(12):1354-66. The American Journal of Respiratory and Critical Care Medicine is an official journal of the American Thoracic Society.
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