| AFPP | acute fibropurulent pneumonia |
|---|---|
| AFSP | acute fibrinoserous pneumonia |
| BEAP | bronchiectasis, eosinophilia, asthma, pneumonia |
| BOOP | bronchiolitis obliterans-organizing pneumonia |
| CEP | chronic eosinophilic pneumonia; chronic erythropoietic porphyria; congenital erythropoietic porphyri... |
| traumatic progressive encephalopathy | A chronic progressive brain damage resulting from multiple brain injuries, e.g., dementia pugilistica. (05 Mar 2000) |
|---|---|
| essential progressive atrophy of iris | Progressive atrophy of the iris without inflammatory signs, characterised by patchy loss of all layers of the iris with hole formation, migration of the pupil, degeneration of the corneal endothelium, peripheral anterior synechiae, and secondary glaucoma; usually unilateral, predominantly affecting women in their middle years. (05 Mar 2000) |
| lenticular progressive degeneration | <gastroenterology, neurology> An inherited (autosomal recessive) disorder where there is excessive quantities of copper in the tissues, particularly the liver and central nervous system. Wilson's disease causes the body to absorb and retain copper. The copper deposits in the liver, brain, kidneys and eyes. Complications include dementia and liver failure. Symptoms include jaundice, vomiting, tremors, weakness and slow stiff movements. Blood tests show serum ceruloplasmin is low. Medications are given to remove the excess copper from the body. Even with life-long treatment, disabling (and life-threatening) side effects are common. Inheritance: autosomal recessive. (27 Sep 1997) |
| leukoencephalopathy, progressive multifocal | Rare demyelinating disease of the central nervous system which develops in immunocompromised patients secondary to lymphoproliferative disease, immunosuppressive therapy, autoimmune disorders, or aids. It is caused by the jc virus, a polyomavirus. (12 Dec 1998) |
| acute interstitial pneumonia | A severe and usually fatal form of pneumonia occurring primarily in infants usually considered a form of hypersensitivity pneumonitis. (05 Mar 2000) |
| alcoholic pneumonia | Pneumonia occurring in patient with alcoholism, usually after a period of intoxication with stupor, resulting in aspiration. (05 Mar 2000) |
| anthrax pneumonia | A form of anthrax acquired by inhalation of dust containing Bacillus anthracis; there is an initial chill followed by pain in the back and legs, rapid respiration, dyspnea, cough, fever, rapid pulse, and extreme cardiovascular collapse. Synonym: anthrax pneumonia, ragpicker's disease, ragsorter's disease, rag-sorter's disease, wool-sorter's pneumonia, woolsorter's disease, wool-sorter's disease. (05 Mar 2000) |
| apex pneumonia | Apical pneumonia, pneumonia of the apex or apices. (05 Mar 2000) |
| aspiration pneumonia | <chest medicine> Refers to the inappropriate passage of food, water, stomach acid, vomit or another foreign material into the lungs. Aspiration, particularly involving gastric acid, will often result in a serious pneumonia. (27 Sep 1997) |
| atypical pneumonia | <chest medicine> This refers to a type of pneumonia that does not follow the typical signs and symptoms of pneumonia. A number of different viral and bacterial agents have been identified which can cause this form of respiratory infection. Examples include Chlamydia pneumonia, psittacosis, Mycoplasma, influenza A or B, adenovirus and Legionella. Antibiotics will be necessary in all but the mildest cases. Symptoms generally improve in less than 2 weeks. (27 Sep 1997) |
| bacterial pneumonia | Infection of the lung with any of a large variety of bacteria, especially Streptococcus pneumoniae(pneumococcus). (05 Mar 2000) |
| bilious pneumonia | Pneumonia following aspiration of gastric contents containing bile. (05 Mar 2000) |
| bronchial pneumonia | <chest medicine> A name given to an inflammation of the lungs which usually begins in the terminal bronchioles. These become clogged with a mucopurulent exudate forming consolidated patches in adjacent lobules. The disease is frequently secondary in character, following infections of the upper respiratory tract, specific infectious fevers and debilitating diseases. In infants and debilitated persons of any age it may occur as a primary affection. Synonym: bronchial pneumonia, bronchoalveolitis, bronchopneumonitis, lobular pneumonia. (11 Jan 1998) |
| bronchiolitis obliterans organizing pneumonia | A disease formerly considered a form of interstitial pneumonia. Its aetiology is obscure but it may be associated with toxic fumes, infection, and connective tissue disease. Clinical symptoms include cough, dyspnea and influenza-like symptoms with the development of the usual interstitial pneumonia in many cases. Obstructive symptoms are limited to smokers. There are patchy polypoid masses of intra-alveolar granulation tissue in small airway lumina and alveolar ducts. "organizing" refers to unresolved pneumonia (in which the alveolar exudate persists and eventually undergoes fibrosis) in which fibrous tissue forms in the alveoli. (12 Dec 1998) |
| bronchiolitis obliterans with organizing pneumonia | Bronchiolitis fibrosa obliterans complicated by pneumonia with organization. Acronym: BOOP (05 Mar 2000) |