| juvenile papillomatosis | A form of fibrocystic disease of the breast in young women, with florid and sclerosing adenosis that microscopically may suggest carcinoma. (05 Mar 2000) |
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| palatal papillomatosis | Closely arranged papules of the palatal mucosa underlying an ill-fitting denture. Synonym: palatal papillomatosis. (05 Mar 2000) |
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| papillomatosis | A disorder with numerous papillomas. (12 Dec 1998) |
| papillomatosis, laryngeal | Warty growths on the vocal cords. most common in young children. Recurrences are, unfortunately, frequent. Remission may occur after several years. Papillomatosis of the larynx can be due to the baby contracting human papilloma virus (HPV) during birth through the vaginal canal from a mother with genital warts (which are due to HPV). Each year, about 300 infants are born with the virus on their vocal cords because of maternal transmission. (12 Dec 1998) |
| confluent and reticulate papillomatosis | Discrete and confluent gray-brown papules of the anterior and posterior mid-chest, spreading gradually; Malassezia furfur has been found in the keratin layer. Synonym: Gougerot-Carteaud syndrome. (05 Mar 2000) |
| subareolar duct papillomatosis | A benign tumour which may clinically resemble Paget's disease, but which is a papillary or solid growth of columnar and myoepithelial cells producing a florid pseudoinfiltrative pattern. Synonym: adenoma of nipple, erosive adenomatosis of nipple. (05 Mar 2000) |
| florid oral papillomatosis | Diffuse involvement of the lips and oral mucosa with benign squamous papillomas; microscopically, it resembles verrucous carcinoma, but is not invasive or localised to a specific area of the oral mucosa. (05 Mar 2000) |
| laryngeal papillomatosis | <radiology> most common laryngeal tumour in kids, probably viral, transbronchial spread: uncommonly (<5%) in patients with large, chronic papillomata, and multiple surgical procedures, nodular lung densities, thin-walled cavities (frequently RUL) (12 Dec 1998) |
| 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) |
| systemic-onset juvenile rheumatoid arthritis | <rheumatology> A form of joint disease, arthritis, that presents with systemic upset. Clinical signs: 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 itself may not be immediately apparent but once apparent, it may persist after the systemic symptoms have resolved. Synonym: Still's disease. (03 Jul 1999) |
| juvenile | Pertaining to youth or childhood, young or immature. (18 Nov 1997) |