| PAP | 1) Prostatic Acid Phosphatase; Àü¸³¼º »ê¼º ÀλêºÐÇØÈ¿¼Ò 2) Primary Atypical Pneumoni... |
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| ALP | acute leukemia protocol; acute lupus pericarditis; alkaline phosphatase; alveolar proteinosis; anter... |
| PAP | pancreatitis-associated protein; Papanicolaou [test]; papaverine; passive-aggressive personality; pa... |
| PAP | Pulmonary Alveolar Proteinosis |
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| proteinosis | A state characterised by disordered protein formation and distribution, particularly as manifested by the deposition of abnormal proteins in tissues. Origin: protein + G. -osis, condition (05 Mar 2000) |
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| alveolar proteinosis | A very rare disease in which a phospholipid is widely distributed in cells and accumulates in the alveolar spaces in the lung. In some cases the underlying cause is unknown. In others it may relate to an infection or an immune system dysfunction. The net effect is a progressive interference in the ability of the lung (alveoli) to exchange oxygen and carbon dioxide. Symptoms include cough, weight loss, fatigue, shortness of breath and nail abnormalities (clubbing). Chest X-ray may show infiltrates, but a bronchoscopy with trans-tracheal biopsy is necessary to make a tissue diagnosis or alveolar proteinosis. Spontaneous remission may occur in some individuals while complete respiratory failure occurs in others. (27 Sep 1997) |
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| pulmonary alveolar proteinosis | <radiology> Overproduction of surfactant which can lead to alveolar (end-air-space) filling, peak age: 20 - 50 yrs, 33% asymptomatic, treatment: lavage Findings: bat-wing alveolar infiltrate, no interstitial disease, no adenopathy (12 Dec 1998) |
| lipoid proteinosis | <disease> A familial disease occurring in the course of latent diabetes, marked by yellowish nodules due to deposits of a protein-lipid complex on the oral tongue and sublingual and faucial areas, translucent keratotic papillomatous eyelid lesions, keratotic lesions on the extremities, and hoarseness. It is due to a disturbance of lipid metabolism with autosomal recessive inheritance and is frequently associated with intracranial calcifications. inheritance: autosomal recessive. Synonym: hyalinasis cutis et mucosae, lipoidosis cutis et mucosae, Urbach-Wiethe disease. (05 Mar 2000) |
| proteinosis |
the accumulation of excess protein in the tissues.
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