| ¿µ¹® | cellulitis | ÇÑ±Û | ¿¬Á¶Á÷¿° |
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| JRA | Juvenile Rheumatoid Arthritis; ¿¬¼Ò±â ·ù¸¶ÅäÀÌµå °üÀý¿° = Juvenile Chronic Arthritis; ¿¬¼Ò±â ¸¸¼º °üÀý... |
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| JD | jejunal diverticulitis; juvenile delinquent; juvenile diabetes |
| HSM Syndrome | juvenile-familial Endocrinopathy Hypoparathyroidism Addison's Disease Menillansis |
| LCP Disease | Legg-Calve-Perthes Disease ? Stages of LCP Disease(= Juvenile Idiopathic AVN) &nb... |
| DJOA | dominant juvenile optic atrophy |
| AR-JP | Autosomal recessive juvenile parkinsonism |
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| GJP | Generalized Juvenile Periodontitis |
| IJ | infective juvenile |
| JA | Juvenile Arthritis |
| JCA | Juvenile Chronic Arthritis |
| gangrenous cellulitis | Infection of soft tissue with anaerobes, usually including clostridia, producing extensive tissue necrosis. Synonym: necrotizing cellulitis. (05 Mar 2000) |
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| cellulitis | <dermatology> An acute, diffuse, spreading, oedematous, suppurative inflammation of the deep subcutaneous tissues and sometimes muscle, which may be associated with abscess formation. It is usually caused by infection of an operative or traumatic wound, burn or other cutaneous lesion by various bacteria, but group A streptococci and Staphylococcus aureus are the most common aetiological agents. Cellulitis may also occur in immunocompromised hosts or it may follow erysipelas. It tends to spread to tissue spaces and cleavage planes owing to bacterial elaboration of large amounts of hyaluronidases that, break down polysaccharide ground substance, fibrinolysins that digest fibrin barriers and lecithinases that destroy cell membranes. Clinical manifestations include an area of oedema, warmth and tenderness with indistinct margins. Compare: erysipelas. (13 Nov 1997) |
| pelvic cellulitis | <medicine> Inflammation of the cellular tissue in the vicinity of the uterus. Origin: NL. See Para-, and Metritis. Source: Websters Dictionary (01 Mar 1998) |
| phlegmonous cellulitis | An obsolete term for diffuse phlegmon. (05 Mar 2000) |
| necrotizing cellulitis | Synonym: gangrenous cellulitis. (05 Mar 2000) |
| dissecting cellulitis | perifolliculitis abscedens et suffodiens |
| elbow, cellulitis of the | Inflammation of the skin around the elbow due to infection (cellulitis) commonly occurs as a result of abrasions or puncture wounds permitting bacteria on the surface of the skin to invade the deeper layers of the skin. This causes inflamed skin characterised by heat, redness, warmth, and swelling. The most common bacteria that cause cellulitis include Staphylococcus ( Staph ) and Streptococcus ( Streop ). One can have an associated low-grade fever. Cellulitis generally requires antibiotic treatment, either orally or intravenously. Heat application can help in the healing process. (12 Dec 1998) |
| eosinophilic cellulitis | <syndrome> Recurrent cellulitis followed by brawny edematous skin lesions, or a less acute presentation of papular, annular, or gyrate skin lesions which are sometimes urticarial; affected skin and subcutis are heavily infiltrated by eosinophils and histiocytes, with scattered small necrotic foci (flame figures) of varied aetiology; sometimes follows an arthropod bite. Synonym: eosinophilic cellulitis. (05 Mar 2000) |
| epizootic cellulitis | A highly contagious viral disease caused by equine arteritis virus, member of the family Togaviridae, and characterised by a high fever and respiratory and digestive tract signs; the essential lesions involve smaller arteries, with necrosis which may be followed by thrombosis, infarction, haemorrhages, and oedema; abortion is a common result. Synonym: epizootic cellulitis, equine typhoid. (05 Mar 2000) |
| arthritis, juvenile rheumatoid | Rheumatoid arthritis of children occurring in three major subtypes defined by the symptoms present during the first six months following onset: systemic-onset (still's disease, juvenile-onset) polyarticular-onset, and pauciarticular-onset. Adult-onset cases of still's disease (still's disease, adult-onset) are also known. Only one subtype of juvenile rheumatoid arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. (12 Dec 1998) |
| benign juvenile melanoma | A benign, slightly pigmented or red superficial small skin tumour composed of spindle-shaped, epithelioid, and multinucleated cells that may appear atypical; most common in children, but also appearing in adults. Synonym: benign juvenile melanoma, epithelioid cell nevus, spindle cell nevus. (05 Mar 2000) |
| rheumatoid arthritis, systemic-onset juvenile | Also known as systemic-onset juvenile chronic arthritis. Still's disease presents with systemic (bodywide) illness including high intermittent fever, a salmon-coloured skin rash, swollen lymph glands, enlargement of the liver and spleen, and inflammation of the lungs (pleuritis) and around the heart (pericarditis). The arthritis may not be immediately apparent but it does appear and may persist after the systemic symptoms are gone. (12 Dec 1998) |
| periodontitis, juvenile | Localised periodontitis in teenagers and young adults. The onset is during the circumpubertal period but the diagnosis can be made beyond puberty. Lesions are confined predominantly to the first permanent molars or incisors and the distribution of lesions is usually symmetrical. The gingiva may appear normal. The lesions are highly active immediately following puberty but later destruction may slow or cease spontaneously. The disease is four times more prevalent in females than males and more prevalent in african americans than in other races or ethnic groups. (12 Dec 1998) |
| xanthogranuloma, juvenile | Benign disorder of infants and children characterised by multiple nodules with lipid-laden, non-langerhans-cell histiocytes. (12 Dec 1998) |
| systemic-onset juvenile chronic arthritis | See: Systemic-onset juvenile rheumatoid arthritis (still's disease). (12 Dec 1998) |
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