Oct 7, 2020 Technology by admin

Original Article from The New England Journal of Medicine — Bronchiectasis: Treatment and Prevention. Original Article from The New England Journal of Medicine — The Pathogenesis of Bronchiectasis. 4 days ago Read the latest NEJM Case Records of the Massachussetts General Bronchiectasis may develop in patients with a history of recurrent.

Author: Brataxe Tegor
Country: Kuwait
Language: English (Spanish)
Genre: Relationship
Published (Last): 7 January 2015
Pages: 468
PDF File Size: 16.59 Mb
ePub File Size: 16.85 Mb
ISBN: 981-6-97422-752-9
Downloads: 87041
Price: Free* [*Free Regsitration Required]
Uploader: Tygorr

Bronchiectasis is characterized by irreversible damage of the airways that results in dilatation.

A Woman with Recurrent Sinusitis, Cough, and Bronchiectasis

Cystic fibrosis is a recessive genetic disease that is caused by mutations in both alleles of the CFTR gene, which encodes the cystic fibrosis transmembrane conductance regulator CFTR. Primary ciliary dyskinesia can also cause left—right asymmetry.

Request to Join has invited you to join this group. Describe features of primary ciliary dyskinesia.

A Woman with Recurrent Sinusitis, Cough, and Bronchiectasis | NEJM Resident

Log in via Email. The CFTR protein forms a chloride channel that is critical to efficient mucus transport. Back to Social Login. Primary ciliary dyskinesia is a congenital, autosomal recessive disorder that is characterized by immotile or dyskinetic cilia.


This is the target of action of the drugs lumacaftor and bronchkectasis.

In addition to impaired airway clearance, fertility problems can arise in males as a result of impaired spermatozoa motility and in females as a result of impaired ciliary nejjm in the oviduct. There are close to recognized CFTR mutations, and each one confers a different degree of diminished chloride ion transport. In bronchiectadis, the qualifying mutations for the administration of ivacaftor were expanded to include DH. Bronchiectasis may develop in patients with a history of recurrent pneumonia, particularly those with chronic aspiration.

Create your account Back to Social Login.

We will not share your email with anyone. Patients with immunodeficiency syndromes are at high risk for the development of bronchiectasis. Show or Hide the password you are typing. Therefore, nodal ciliary dysfunction can produce dextrocardia, situs inversus totalis, and situs ambiguus.

Many lung infections can result in the development of bronchiectasis, including those caused by Mycobacterium tuberculosis and Bordetella pertussis. The primary defect that is caused by the Phedel mutation is that the CFTR protein is synthesized but misfolded, which keeps it from reaching the cell nejmm.

  KB3926QF A1 PDF

In some people, inhalation of Aspergillus fumigatus provokes a brisk allergic response that is characterized by eosinophilia and a high level of IgE bronchiecyasis. Password must be at least 8 characters. With the administration of these treatments at cystic fibrosis—specific treatment centers, median survival has increased from The DH mutation is considered to be a partial-function mutation that results in diminished ion transport.

This type of mutation is the target of the drug ivacaftor, which restores partial ion transport. Mutations in CFTR disrupt sodium absorption, chloride secretion, and water transport, leading to the development of viscous mucus that adheres to the airway and impairs bacterial clearance. A hypersensitivity response, known as allergic bronchopulmonary aspergillosis, may ensue, leading to a cycle of bronchial inflammation, mucoid impaction, and bronchial obstruction that results in bronchiectasis.

What are some of the causes of bronchiectasis?