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  2. Lymphangioleiomyomatosis - Wikipedia

    en.wikipedia.org/wiki/Lymphangioleiomyomatosis

    Preservation of lung volumes in the presence of increased interstitial markings is a radiographic hallmark of LAM that helps distinguish it from most other interstitial lung diseases, in which alveolar septal and interstitial expansion tend to increase the lung's elastic recoil properties and decreased lung volumes.

  3. 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 ...

  4. Pulmonary fibrosis - Wikipedia

    en.wikipedia.org/wiki/Pulmonary_fibrosis

    [1] [3] Diagnosis may be based on symptoms, medical imaging, lung biopsy, and lung function tests. [1] No cure exists and treatment options are limited. [1] Treatment is directed toward improving symptoms and may include oxygen therapy and pulmonary rehabilitation. [1] [4] Certain medications may slow the scarring. [4] Lung transplantation may ...

  5. Pneumonia - Wikipedia

    en.wikipedia.org/wiki/Pneumonia

    Pneumonia is an inflammatory condition of the lung primarily affecting the small air sacs known as alveoli. [3] [14] Symptoms typically include some combination of productive or dry cough, chest pain, fever, and difficulty breathing. [15]

  6. Restrictive lung disease - Wikipedia

    en.wikipedia.org/wiki/Restrictive_lung_disease

    Restrictive lung diseases are a category of extrapulmonary, pleural, or parenchymal respiratory diseases that restrict lung expansion, [2] resulting in a decreased lung volume, an increased work of breathing, and inadequate ventilation and/or oxygenation. Pulmonary function test demonstrates a decrease in the forced vital capacity.

  7. Idiopathic pulmonary fibrosis - Wikipedia

    en.wikipedia.org/wiki/Idiopathic_pulmonary_fibrosis

    The tissue in the lungs becomes thick and stiff, which affects the tissue that surrounds the air sacs in the lungs. [7] Symptoms typically include gradual onset of shortness of breath and a dry cough. [1] Other changes may include feeling tired, and clubbing abnormally large and dome shaped finger and toenails. [1]

  8. Sarcoidosis - Wikipedia

    en.wikipedia.org/wiki/Sarcoidosis

    The disease usually begins in the lungs, skin, or lymph nodes. [2] Less commonly affected are the eyes, liver, heart, and brain, though any organ can be affected. [2] The signs and symptoms depend on the organ involved. [2] Often, no symptoms or only mild symptoms are seen. [2]

  9. Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia

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

    The morbidity associated with DIPNECH is due to the associated obstructive lung disease. The lung disease tends to be slowly progressive, but given enough time can lead to significant disability and require supplemental oxygen therapy. [8] There have been reports of lung transplantation in the setting of end-stage DIPNECH. [11]

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