Search results
Results from the WOW.Com Content Network
Differential diagnosis includes non-specific interstitial pneumonia, pulmonary Langerhans cell histiocytosis, respiratory bronchiolitis-associated interstitial lung disease, and hypersensitivity pneumonia. DIP is primarily treated by quitting smoking, but it may not be enough in all cases. In moderate to severe cases, corticosteroids are used.
Lobar pneumonia usually has an acute progression. Classically, the disease has four stages: [1] Congestion in the first 24 hours: This stage is characterized histologically by vascular engorgement, intra-alveolar fluid, and small numbers of neutrophils, often numerous bacteria. Grossly, the lung is heavy and hyperemic.
The lung tissue lies within the same visceral pleura as the lobe in which it occurs. [1] Males and females are equally affected. [1] The arterial supply is usually derived from the lower thoracic or upper abdominal aorta. Venous drainage is usually to the left atrium via pulmonary veins establishing a left to left shunt.
High-resolution CT image showing ground-glass opacities in the periphery of both lungs in a patient with COVID-19 (red arrows). The adjacent normal lung tissue with lower attenuation appears as darker areas. Ground-glass opacity (GGO) is a finding seen on chest x-ray (radiograph) or computed tomography (CT) imaging of the lungs.
While patchy bilateral disease is typical, there are unusual variants of organizing pneumonia where it may appear as multiple nodules or masses. One rare presentation, focal organizing pneumonia, may be indistinguishable from lung cancer based on imaging alone, requiring biopsy or surgical resection to make the diagnosis. [20]
There are ten bronchopulmonary segments in the right lung: three in the superior lobe, two in the middle lobe, and five in the inferior lobe. Some of the segments may fuse in the left lung to form usually eight to nine segments (four to five in the upper lobe and four to five in the lower lobe.
Pulmonary artery stenosis (PAS) is a narrowing of the pulmonary artery.The pulmonary artery is a blood vessel moving blood from the right side of the heart to the lungs. . This narrowing can be due to many causes, including infection during pregnancy, a congenital heart defect, a problem with blood clotting in childhood or early adulthood, or a genetic ch
Congenital pulmonary airway malformation (CPAM), formerly known as congenital cystic adenomatoid malformation (CCAM), is a congenital disorder of the lung similar to bronchopulmonary sequestration. In CPAM, usually an entire lobe of lung is replaced by a non-working cystic piece of abnormal lung tissue.