Image diagnoses for "red"
857 results with 4400 images

Naevus flammeus (Port-wine stain): sharply defined red vascular nevus that affects the upper and lower eyelid as well as the temporal region.

Dermatitis bullosa pratensis: Stripy, itchy and burning erythema with blistering on the leg after a walk through a high meadow with subsequent tanning.

Carcinoma, verrucous, cauliflower-like, ulcerated tumor in the genital region with right-sided lymph node metastasis that has existed for years.

Lupus erythematosus: cutaneous chronic (scarring) lupus erythematosus (chronic discoid lupus erythematosus). years of progression with circumscribed red scarring plaques (circle - with whitish scarring - atrophic area without follicular structure): arrow: dermal melanocytic nevus.

Scleroderma systemic: edematous swelling of the hands and fingers. when stretching the fingers, white discoloration of the tense skin areas (see right index finger) occurs. Raynaud's syndrome known for several years. increased sensitivity to cold, rheumatoid joint complaints, ANA:1:620; SCL70AK+.

Mycosis fungoides: tumor stage. 53-year-old man with multiple, disseminated, 1.0-5.0 cm large, in places also large, moderately itchy, clearly consistency increased, red, rough, confluent plaques (nodules)

Dermatosis IgA-lineare: detailed picture with circulatory smaller and larger red blisters on urticarial background.

Lingua plicata in Melkersson-Rosenthal syndrome

Melanoma, malignant, amelanotic. 1.5 x 1.6 cm measuring, sharply defined, non-pigmented, white-red tumor with whitish to yellowish, verrucous, partly erosive changed surface on the lower leg of a 70-year-old patient.

Acrodermatitis continua suppurativa: for years a chronic recurrent clinical picture with painful pustules, nail destruction with formation of erosive areas

Granuloma anulare subcutaneum. several, moderately pressure-dolent, skin-coloured to brown-red, deeply dermal or subcutaneously situated, moderately coarse, shifting, 0.4-1.5 cm large nodules and nodes. existence for years (5-15 years).

Angioimmunoblastic T-cell lymphoma: Dress syndrome in AIP.  Figure taken from: Mangana Jet al. (2017)

Malformations, vascular. mixed venous/capillary malformation with predominant subcutaneous venous part.

Erythema anulare centrifugum: characteristic (fresh) lesions with peripherally progressive plaques, which are peripherally palpable as well limited (like a wet wolfaden) Histological clarification necessary.

Squamous cell carcinoma in actinically damaged skin.:since > 1year, slowly growing, very firm, little pain-sensitive lump, which (at the time of examination) was no longer movable on its support. Bleeding repeatedly.

Infant hemangioma. scrotal and perineal hemangioma and aggregated papules in a 2-month-old boy. From day 6-7 after birth red spots appeared at first on the scrotum, which then increased in size and spread to the anus.

Plaqueform mucinosis of the skin: follicle-accentuating (peau d'orange) deposits of mucin in the skin.

Kaposi sarcoma HIV-associated: flat, symptomless plaques; HIV infection known for several years.

Lichen planus of the vulva: itching for months. 35-year-old female patient with veil-like white discolouration of the large labia marked by arrows. Fig. from Eiko E.Petersen, Colour Atlas of Vulva Diseases, with the permission of Kaymogyn GmbH Freiburg.