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CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
bullous congenital ichthyosiform erythroderma Diffusely red, eroded skin at birth, with subsequent scaling, tending to improve in later life, characterised by generalised epidermolytic hyperkeratosis and autosomal dominant inheritance.
See: epidermolytic hyperkeratosis.
Synonym: generalised epidermolytic hyperkeratosis, ichthyismus hystrix, ichthyosis hystrix.
(05 Mar 2000)
congenital ichthyosiform erythroderma A genodermatosis characterised by diffuse chronic erythema and scale formation which may be separated into bullous and nonbullous forms.
Synonym: ichthyosiform erythroderma, ichthyosis spinosa, keratoma malignum.
(05 Mar 2000)
nonbullous congenital ichthyosiform erythroderma Erythroderma or a collodion membrane at birth, usually without improvement during childhood, characterised by proliferation of epidermal keratinocytes with lipid accumulation; autosomal recessive inheritance.
(05 Mar 2000)
ichthyosiform erythroderma A genodermatosis characterised by diffuse chronic erythema and scale formation which may be separated into bullous and nonbullous forms.
Synonym: ichthyosiform erythroderma, ichthyosis spinosa, keratoma malignum.
(05 Mar 2000)
ichthyosiform erythroderma, congenital Designation for several severe forms of ichthyosis, present at birth, that are characterised by hyperkeratotic scaling. Infants may be born encased in a collodion membrane which begins shedding within 24 hours. This is followed in about two weeks by persistent generalised scaling. The forms include bullous (hyperkeratosis, epidermolytic), non-bullous (ichthyosis, lamellar), wet type, and dry type.
(12 Dec 1998)
acquired nevus A melanocytic nevus that is not visible at birth, but appears in childhood or adult life.
(05 Mar 2000)
balloon cell nevus A nevus in which many of the cells are large, with clear cytoplasm.
(05 Mar 2000)
basal cell nevus A hereditary disease noted in infancy or adolescence, characterised by lesions of the eyelids, nose, cheeks, neck, and axillae, appearing as uneroded flesh-coloured papules, some becoming pedunculated, and histologically indistinguishable from basal cell epithelioma; also noted are punctate keratotic lesions of the palms and soles; the lesions usually remain benign, but in some cases ulceration and invasion occur and are evidence of malignant change; autosomal dominant inheritance.
(05 Mar 2000)
basal cell nevus syndrome <syndrome> An inherited group of defects which involve abnormalities of the skin, eyes, nervous system, endocrine, glands and bones.
The condition is characterised by an unusual facial appearance and a predisposition for skin cancer.
(27 Sep 1997)
bathing trunk nevus These large pigmented (often hairy) congenital nevi are important because of their increased risk (10 to 15%) of conversion into malignant melanoma. A biopsy can confirm if cells have turned malignant. Any change in a pre-existing nevus should prompt a physician evaluation.
(27 Sep 1997)
Becker's nevus A nevus first seen as an irregular pigmentation of the shoulders, upper chest, or scapular area, gradually enlarging irregularly and becoming thickened and hairy.
Synonym: pigmented hair epidermal nevus.
(05 Mar 2000)
blue nevus A dark blue or blue-black nevus covered by smooth skin and formed by heavily pigmented spindle-shaped or dendritic melanocytes in the reticular dermis.
Synonym: Jadassohn-Tieche nevus.
(05 Mar 2000)
blue rubber bleb nevus syndrome <radiology> Bean syndrome, sporadic (some autosomal dominant), rubbery, raised blue-black skin nevi (cavernous haemangiomata, 0.1 - 5 cm), GI mucosal haemangiomata, bowel: polypoid filling defects of varying sizes, visceral haemangiomata (by angio) associated with: leukaemia, medulloblastoma, hypernephroma, Mafucci syndrome More info: blue rubber bleb nevus syndrome
(12 Dec 1998)
capillary nevus Capillary haemangioma of the skin.
(05 Mar 2000)
verrucous nevus A skin-coloured or darker wartlike, often linear, lesion appearing at birth or early in childhood, and occurring in various sizes and locations, single or multiple.
(05 Mar 2000)
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