Related Experiment Video
Updated: May 31, 2025

07:53
Multidimensional Coculture System to Model Lung Squamous Carcinoma Progression
Published on: March 17, 2020
7.1K
Lung Cancers Associated with Cystic Airspaces
Clara Valsecchi1, Francesco Petrella2, Stefania Freguia3
1Clinic of Radiology EOC, Istituto Imaging della Svizzera Italiana (IIMSI), Via Tesserete 46, 6900 Lugano, CH, Switzerland.
Cancers
|January 25, 2025
Summary
Early detection of lung cancer is crucial. Lung cancers in cystic airspaces are understudied but awareness can improve diagnosis and reduce mortality.
Area of Science:
- Oncology
- Radiology
- Pulmonology
Background:
- Lung cancer is a leading cause of cancer-related death globally.
- Computed tomography (CT) screening increases the detection of early-stage lung cancers.
- Lung cancers associated with cystic airspaces are an understudied subgroup.
Purpose of the Study:
- To highlight the significance of identifying lung cancers associated with cystic airspaces.
- To emphasize the need for increased radiologist awareness regarding these specific lung cancers.
- To underscore the potential for improved early diagnosis and reduced mortality.
Main Methods:
- Review of existing literature on lung cancers associated with cystic airspaces.
- Analysis of radiological and pathological features.
- Estimation of prevalence based on delayed diagnoses.
Main Results:
- Lung cancers in cystic airspaces exhibit complex cystic components and evolve over time.
- Adenocarcinoma is the predominant histological type, often peripherally located.
- These cancers may be misdiagnosed as inflammatory or emphysematous changes on CT scans.
Conclusions:
- Lung cancers associated with cystic airspaces are estimated to account for a significant portion of delayed diagnoses.
- Enhanced radiologist awareness is critical for timely identification.
- Improved detection can lead to cost-effective reductions in lung cancer mortality.
More Related Videos
Related Concept Videos
Other Pulmonary Disorders
799
Respiratory disorders encompass a range of conditions with varying levels of severity. Asthma, marked by chronic airway inflammation and hypersensitivity, is one such condition. It can lead to airway obstruction due to factors like bronchial spasms, mucosal edema, increased mucus secretion, or epithelial damage. Asthma triggers are diverse, ranging from allergens to emotional upset, and treatment focuses on both immediate relief through bronchodilators and long-term inflammation suppression.
799
Cystic Fibrosis: Pathogenesis
182
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
182
Gross Anatomy of the Lungs
1.5K
The lungs are a pair of vital organs connected to the trachea via the left and right bronchi. The base of these organs meets the dome-shaped muscle known as the diaphragm. Encased by the pleurae, the lungs contact the mediastinum. The right lung is shorter yet wider, and has a larger volume than the left lung. The left lung has an indentation known as the cardiac notch. The superior region of the lungs is referred to as the apex, whereas the base is the lower region near the diaphragm. The...
1.5K
Pleura of the Lungs
1.5K
The lungs are nestled in a cavity, shielded by the pleura. The pleura, a form of serous membrane, wraps around each lung. This membrane arrangement consists of two layers: the visceral and parietal pleurae. The visceral pleura lines the surface of the lungIn contrast, the parietal pleura is the outer layer and contacts to the thoracic wall, the mediastinum, and the diaphragm. The hilum is the point of connection between the visceral and parietal layers. The space between the parietal and...
1.5K
Cystic Fibrosis: Management
139
Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic...
Sinus disease and chronic...
139
lncRNA - Long Non-coding RNAs
8.5K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
8.5K

