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.

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Describe features of primary ciliary dyskinesia. Therefore, nodal ciliary dysfunction can produce dextrocardia, situs inversus totalis, and situs ambiguus.

Password must be at least 8 characters. 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 surface.

Request to Join has invited you to join this group. This is the target of action of the drugs lumacaftor and tezacaftor.

A Woman with Recurrent Sinusitis, Cough, and Bronchiectasis

Patients with immunodeficiency syndromes are at high risk for the development of bronchiectasis. With the administration of these treatments at cystic fibrosis—specific treatment centers, median survival has increased from bronchectasis What are some of the causes of bronchiectasis?


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 ndjm in the oviduct. Create your account Back to Social Login. Many lung infections can result in the development of bronchiectasis, including those caused by Mycobacterium tuberculosis and Bordetella pertussis.

The CFTR protein forms a chloride channel that is critical to efficient mucus transport. Log in via Email. This type of mutation is the target of the drug ivacaftor, which restores partial ion transport.

There are close to recognized CFTR mutations, and each one confers a different degree of diminished chloride ion transport. Inthe qualifying mutations for the administration of bronchiectwsis were broncuiectasis to include DH. In some people, inhalation of Aspergillus fumigatus provokes a brisk allergic response that is characterized by eosinophilia and a high level of IgE antibodies. 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.

Primary ciliary dyskinesia is a congenital, autosomal recessive disorder that is characterized by immotile or dyskinetic cilia. The DH mutation is considered to be a partial-function mutation that results in diminished ion transport. A hypersensitivity response, known as allergic bronchopulmonary aspergillosis, may ensue, leading to a cycle of bronchial vronchiectasis, mucoid impaction, and bronchial obstruction that results in bronchiectasis.


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

Show or Hide the password you are typing. 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.

Bronchiectasis is characterized by irreversible damage of the airways that results in dilatation. We will not share your email with anyone.

Back to Social Login. Primary ciliary dyskinesia can also cause left—right asymmetry. Bronchiectasis may broncjiectasis in patients with a history of recurrent pneumonia, particularly those with chronic aspiration.