Image diagnoses for "red"
876 results with 4456 images

Dermatitis contactallergic. typical for the allergic pathogenesis of eczema is the blurred, scattering limitation of the inflammatory zone.

Mycobacteriosis, atpic. lymphatic (sporotrichoid) spread of painless red nodules.

Eczema atopic (overview): severe, universal (erythrodermic) atopic eczema. exacerbation phase since about 3 months. patient with rhinitis and conjunctivitis in pollinosis. total IgE >1.000IU.

Infant hemangioma (series: findings after 2 years): No therapy, extensive regression of the node.

Remark: In the meantime the hemangioma is completely healed (except for some telangiectasias).

Prurigo simplex subacuta:0.3-0.4 cm large, red, centrally eroded or ulcerated, moderately sharply defined, interval-like, violently itching papules, which are shown in the present image detail in different stages of development.

Lupus erythematosus so-called chilbalin lupus: recurrent course for years; bluish-livid, painful plaques reminiscent of frostbite (chilblain).

Keloids: Flat, smooth-surfaced, firm, red nodules, increased vascular drawing. In this clinical picture a dermatofibrosarcoma protuberans can be excluded by differential diagnosis.

Dermatomyositis

Xanthomas, eruptive: 0.1-0.3 cm in size, yellow-brown, flat raised, superficially smooth and shiny, disseminated, clearly consistent papules in dense seeding in a 45-year-old patient with known hyperlipoproteinemia type IV. Seeding increasing since 6 months preferably on trunk and back. Clinic is typical, histology is diagnostic.

Purpura pigmentosa progressiva: aetiologically unexplained (medication?) pronounced clinical picture that has been changing for several months with symmetrically distributed, disseminated, non-itching, yellow-brown, spots (detailed picture).

Felty syndrome. Detail enlargement of the above findings.

Pyoderma gangraenosum: deep, painful ulcer that has existed for several months; ulcerative colitis ulcerosa that is located at the base of the tract.

Dorsal cyst, mucoid: painless, approximately 1.0 cm large, skin-coloured, plumply elastic, surface-smooth "nodule" (cyst) which has existed for about 1 year and from which a gelatinous substance has emptied itself (crust-covered part) under pressure, whereby the whole nodule has disappeared.

Alopecia, scarring. dynamically progressing, increasing inflammatory, scarring hairlessness in generalized dyskeratosis follicularis.

Lymphomatoid papulosis. 64-year-old patient with a history of 15 years. recurrent, intermittent course with formation of 4-10 painless nodules, which grow to the size shown here within a few days. rapid central ulceration. healing within 8-10 weeks leaving a sunken scar. recurrent secondary infections of the ulcerated nodules. previously known non-Hodgkin lymphoma in full remission.

Dermatomyositis. Gottron papules in a 72-year-old woman. Smaller, striated, reddish-livid papules appear, which confluent in the region of the end phalanges to form flat plaques. Strongly pronounced nail fold capillaries on dig. III and V. The Keining sign was strongly positive in the clinical examination.

Onychogrypose: crumbly onychodystrophy with excessive thickening of the fingernail; previously known, long-standing mycosis fungoides.

Urticaria pigmentosa: general view: about 0.5-1.0cm large, disseminated, oval or round, brownish-red spots. only when rubbed, increased redness of the spots with accompanying itching. also in warm showers or baths increased redness and clearly palpable elevation of the lesions.

Infantile acrolocalized papulo-vesicular syndrome: Papulo-vesicular exanthema with environmental erythema of the upper extremity in an 8-month-old boy.

Pityriasis rosea: typical exanthema of bright red papules and flat plaques on the trunk and proximal extremities, some with typical Collerette scaling. there is little itching. duration of existence at first presentation 2 weeks. pat male, 29 yrs.