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  2. Interstitial lung disease - Wikipedia

    en.wikipedia.org/wiki/Interstitial_lung_disease

    Interstitial lung disease (ILD), or diffuse parenchymal lung disease (DPLD), [3] is a group of respiratory diseases affecting the interstitium (the tissue) and space around the alveoli (air sacs) of the lungs. [4] It concerns alveolar epithelium, pulmonary capillary endothelium, basement membrane, and perivascular and perilymphatic tissues. It ...

  3. Idiopathic pulmonary fibrosis - Wikipedia

    en.wikipedia.org/wiki/Idiopathic_pulmonary_fibrosis

    IPF is one specific presentation of idiopathic interstitial pneumonia (IIP), which is in turn a type of ILD, also known as diffuse parenchymal lung disease (DPLD). [citation needed] The 2002 American Thoracic Society/European Respiratory Society (ATS/ERS) classification of IIPs was updated in 2013. [10]

  4. Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia

    en.wikipedia.org/wiki/Diffuse_idiopathic...

    Pulmonary function: increased residual volume, increased total lung capacity, fixed obstruction, low diffusing capacity of the lung for carbon monoxide that corrects with alveolar volume; High-resolution CT scan: diffuse pulmonary nodules 4–10 mm, greater than 20 nodules, mosaic attenuation or air trapping in greater than 50% of the lung

  5. List of medical abbreviations: D - Wikipedia

    en.wikipedia.org/wiki/List_of_medical...

    DPLD: diffuse parenchymal lung disease: DPM: Doctor of Podiatric Medicine: DPT: diphtheria-pertussis-tetanus (DPT vaccine) DRE: Digital Rectal ExaminationDilated Retinal Exam DRPLA: Dentatorubral-Pallidoluysian Atrophy: DRT: dead right there DS: disease Down syndrome (trisomy 21) diopters sphere DSA: digital subtraction angiography Donor ...

  6. Idiopathic interstitial pneumonia - Wikipedia

    en.wikipedia.org/wiki/Idiopathic_interstitial...

    Idiopathic interstitial pneumonia (IIP), or noninfectious pneumonia [1] are a class of diffuse lung diseases. These diseases typically affect the pulmonary interstitium, although some also have a component affecting the airways (for instance, cryptogenic organizing pneumonitis). There are seven recognized distinct subtypes of IIP. [2]

  7. Pulmonary fibrosis - Wikipedia

    en.wikipedia.org/wiki/Pulmonary_fibrosis

    The actual number may be significantly higher due to misdiagnosis. Typically, patients are in their forties and fifties when diagnosed, while the incidence of idiopathic pulmonary fibrosis increases dramatically after age 50. But loss of pulmonary function is commonly ascribed to old age, heart disease, or more common lung diseases. [40]

  8. Usual interstitial pneumonia - Wikipedia

    en.wikipedia.org/wiki/Usual_interstitial_pneumonia

    The differential diagnosis includes other types of lung disease that cause similar symptoms and show similar abnormalities on chest radiographs. Some of these diseases cause fibrosis, scarring or honeycomb change. The most common considerations include: chronic hypersensitivity pneumonitis; non-specific interstitial pneumonia; sarcoidosis

  9. Acute interstitial pneumonitis - Wikipedia

    en.wikipedia.org/wiki/Acute_interstitial_pneumonitis

    Acute interstitial pneumonitis (also known as acute interstitial pneumonia) is a rare, severe lung disease that usually affects otherwise healthy individuals. There is no known cause or cure. Acute interstitial pneumonitis is often categorized as both an interstitial lung disease and a form of acute respiratory distress syndrome (ARDS).

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