Image diagnoses for "Armpit"
45 results with 80 images

Pemphigus chronicus benignus familiaris: Diagnostically path-breaking, lineal and punctiform erosions during stretching of the skin within a sharply defined focus in the intertriginous regions (accordion phenomenon).

pemphigus chronicus benignus familiaris. multiple, chronically dynamic (very changeable course with weeping), large, red, rough plaques in the armpit area, interspersed with multiple fissures. pronounced foetid smell. diagnostically path-breaking, lineal and punctiform erosions when stretching the skin. nikolski phenomenon I + II positive.

Pemphigus chronicus benignus familiaris: Chronic dynamic (changing course), smearily covered, sharply defined, red, rough plaque with multiple erosions that become gaping and streaky when stretched (accordion phenomenon).

Pemphigus chronicus benignus familiaris: chronic, extremely therapy-resistant, varying in size, sharply defined, rough, red, marginal plaques in the armpit area with marginal Collerette-like scaling

Psoriasis vulgaris, detail section: Chronic dynamic plaque in the axilla of a 6-year-old girl, occurring in recurrent attacks and existing for 10 days, increasing, solitary, red, rough, covered with cap-like scales.

Scabies. Disseminated papules, single ductal structures in the axilla.

Steatocystoma multiplex: Multiple, for about 6-7 years persistent, up to 6 mm large, whitish papules in the right axilla of a 25-year-old female patient.

Acanthosis nigricans benigna: symmetric, black-brown hyperpigmentations with velvety, partly also verrucous plaques. blurred demarcation from the surroundings. no detectable underlying disease.

Fibroma molle with Acanthosis nigricans

Fibroma molle. numerous, stalked, pendulous, soft, skin-coloured or slightly brownish, symptomless outgrowths in the area of the axilla

Bending atopic eczema; skin lesions in a 13-year-old girl; positive atopic FA; EA: pollinosis known; IgE>100IU; in infancy milk crust; for weeks now, in the area of both axils therapy-resistant, blurred, reddened, slightly scaly, moderately itchy plaques.

Lichen sclerosus of the axilla: large, less symptomatic, whitish, also reddish, atrophic shiny plaque; blurred, feathered border.

Pemphigus chronicus benignus familiaris: chronic, extremely therapy-resistant, sharply defined, rough, red,border-emphasized plaques in the area of the armpit; in the surrounding area, some already healed areas.

Psoriasis inversa, minus variant: discrete psoriatic affection of the axilla.

Erythrasma: sharply defined, extensive, non-itching brownish discoloration in the armpit area.

Hyalinosis cutis et mucosae: extensive yellowish deposits in the area of both axillae.

Lichen planus pigmentosus: extensive post-inflammatory pigmentation, no itching.

Scabies in a 3-year-old child: a generalized clinical picture that has been present for several months, with massive itching, disseminated scaly papules and plaques.

Acne inversa: severe clinical, therapy-resistant finding in a 52-year-old female patient. existing since the age of 20. conspicuous sausage-shaped scar strands.

Extramammary Paget's disease: Continuously growing focal point with different coloration and consistency for3 years; in the center, 2 red sharply bordered plaques encircled by an only slightly accentuated erythema.

Trichobacteriosis axillaris: yellow-coloured plaque that is difficult to strip off and envelops the hair; usually penetrating axillary sweat odour.

Mycosis fungoides: advanced tumor stage with aggregated red plaques and nodules in the axillary region.

Candidosis intertriginous: unusual pustular candidiasis in a strictly bedridden elderly patient.

Hidradenitis suppurativa: chronically persistent, brownish or reddish livid scarring in the right axilla of a man. multiple, partly florid, red plaques and nodules. also scar fields. strong nicotine abuse for 30 years.