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  2. Diffuse alveolar damage - Wikipedia

    en.wikipedia.org/wiki/Diffuse_alveolar_damage

    The most important factor for treating DAD or ARDS is to treat the underlying cause of the injury to the lungs, [9] for example pneumonia or sepsis. These patients will have problems with oxygenation, meaning they will likely need a breathing tube , medications to keep them comfortable (sedative, paralytic, and/or analgesic), and a mechanical ...

  3. Pulmonary hemorrhage - Wikipedia

    en.wikipedia.org/wiki/Pulmonary_hemorrhage

    Infant prematurity is the factor most commonly associated with pulmonary hemorrhage. Other associated factors are those that predisposed to perinatal asphyxia or bleeding disorders, including toxemia of pregnancy, maternal cocaine use, erythroblastosis fetalis, breech delivery, hypothermia, infection (like pulmonary tuberculosis), Infant respiratory distress syndrome (IRDS), administration of ...

  4. 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 ...

  5. Lymphoproliferative disorders - Wikipedia

    en.wikipedia.org/wiki/Lymphoproliferative_disorders

    Lymphoproliferative disorders are a set of disorders characterized by the abnormal proliferation of lymphocytes into a monoclonal lymphocytosis. The two major types of lymphocytes are B cells and T cells, which are derived from pluripotent hematopoietic stem cells in the bone marrow.

  6. Lymphocytic interstitial pneumonia - Wikipedia

    en.wikipedia.org/wiki/Lymphocytic_interstitial...

    Lymphocytic interstitial pneumonia (LIP) is a syndrome secondary to autoimmune and other lymphoproliferative disorders. Symptoms include fever, cough, and shortness of breath. Lymphocytic interstitial pneumonia applies to disorders associated with both monoclonal or polyclonal gammopathy. [1]

  7. Usual interstitial pneumonia - Wikipedia

    en.wikipedia.org/wiki/Usual_interstitial_pneumonia

    Regardless of cause, UIP is relentlessly progressive, usually leading to respiratory failure and death without a lung transplant. [citation needed] Some patients do well for a prolonged period of time, but then deteriorate rapidly because of a superimposed acute illness (so-called "accelerated UIP"). The outlook for long-term survival is poor.

  8. Necrotizing pneumonia - Wikipedia

    en.wikipedia.org/wiki/Necrotizing_pneumonia

    Necrotizing pneumonia (NP), also known as cavitary pneumonia or cavitatory necrosis, is a rare but severe complication of lung parenchymal infection. [1] [2] [3] In necrotizing pneumonia, there is a substantial liquefaction following death of the lung tissue, which may lead to gangrene formation in the lung.

  9. Chylothorax - Wikipedia

    en.wikipedia.org/wiki/Chylothorax

    A chylothorax is an abnormal accumulation of chyle, a type of lipid-rich lymph, in the pleural space surrounding the lung.The lymphatic vessels of the digestive system normally return lipids absorbed from the small bowel via the thoracic duct, which ascends behind the esophagus to drain into the left brachiocephalic vein.