Lung mass pathophysiology: Difference between revisions
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==Pathophysiology== | ==Pathophysiology== | ||
==Genetics== | |||
EGFR mutations are seen in about 20%- 50% of lung adenocarcinoma (especially in Asian population) | |||
*EGFR mutations are responsible for the constitutive activation of the tyrosine kinase. | |||
*The most frequent mutations are present in exons 18e21 of the EGFR gene. | |||
**Other mutation involves translocations involving the anaplastic lymphoma kinase (ALK) tyrosine kinase are most frequently EML4-ALK fusions and are seen in estimated 10% of patients with lung adenocarcinoma. | |||
==Associated Conditions== | |||
==Gross Pathology== |
Revision as of 16:56, 22 February 2018
Lung Mass Microchapters |
Diagnosis |
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Treatment |
Lung mass pathophysiology On the Web |
American Roentgen Ray Society Images of Lung mass pathophysiology |
Risk calculators and risk factors for Lung mass pathophysiology |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief:
Overview
A lung mass is defined as an opacity in the lungs that is more than 3 cms (or 1 ½ inches) in size. Lung opacity less than 3 cms are classified as lung nodules.
Pathophysiology
Genetics
EGFR mutations are seen in about 20%- 50% of lung adenocarcinoma (especially in Asian population)
- EGFR mutations are responsible for the constitutive activation of the tyrosine kinase.
- The most frequent mutations are present in exons 18e21 of the EGFR gene.
- Other mutation involves translocations involving the anaplastic lymphoma kinase (ALK) tyrosine kinase are most frequently EML4-ALK fusions and are seen in estimated 10% of patients with lung adenocarcinoma.