Image diagnoses for "Macule"
321 results with 1208 images

Purpura thrombocytopenic: line shaped, fresh skin bleeding (diascopically not pushable away) after intensive scratching

ecchymosis syndrome, painful, intermittent manifestation of painful skin bleeding in a 48-year-old man. initial development of oedematous, overheated, pressure-sensitive erythema. subsequent development of skin bleeding and slow expansion of the skin changes. scarless healing after 1-2 weeks. in the present case, there was a severely pronounced clinical picture with multiple accompanying symptoms, especially fever, weight loss, fatigue, muscle and headaches, arthralgia, epistaxis, haemoptysis and haematuria.

Nevus, melanocytic, halo-nevus. solitary, depigmented, oval, sharply defined, smooth, white patch with central, sharply defined, brown, slightly raised papule. 27-year-old patient with multiple halo-nevi is shown here.

Lentigo solaris. detail enlargement: inhomogeneously coloured, light brown, sharply defined spot.

Argyrie: diffuse gray coloration of the facial skin after multiple roll cures due to ulcus ventriculi.

Glomus tumor. reflected light microscopy: Livid striped vascular drawing below the nail plate in the area of the lunula and the eponychium. in this area a punctual, strong pressure pain can be induced.

Naevus fuscocoeruleus ophthalmomaxillaris. irregular, planar, brown to blackish blueish, half-sided pigmentation. half-sided manifestation running along the trigeminal nerve in the cheek area.

Dermatomyositis; acutely occurring, succulent exanthema, massive itching with scratching effects; general fatigue,

Dermatitis perioralis. periorally localized, large red spots, smallest follicular vesicles and papules. perioral dermatitis is characterized by an inflammation-free zone immediately adjacent to the red of the lips. 21-year-old woman with several months of therapy with an extemporaneous formulation containing glucorticoids.

Crest syndrome,numerous telangiectases, sclerosis of the facial skin, periorbital radial wrinkles.

Purpura jaune d'ocre. extensive hyperpigmentation with single congestive hemorrhages (Purpura jaune d'ocre) in the area of the right lower leg in case of a previously known CVI. In addition, there is a short-term, extensive redness (erysipelas) extending from the calf to the knee as well as fever, chills and lymphadenitis.

Erythromelalgia. seizure-like, very painful, hyperemic, reddened and swollen skin of the hands and feet with increased sensitivity to heat. improvement of symptoms by cooling under running water.

rosacea. rosacea erythematosa, stage I of rosacea with individual inflammatory papules and pustules. flat, relatively sharply defined, symmetrical erythema (plaque) of the cheeks with clear protrusion of the follicles (skin pores). no comedones. perioral area remaining free. redness is now permanently present after earlier volatility but with varying intensity. at the same time, a feeling of tension and a slight burning sensation with shearing activity.

Purpura eczematide-like purpura: non-symptomatic (no itching) eczema-like disease that has been recurrent for months in a completely healthy patient (no history of medication).

Stage I-IIrosacea (rosacea papulopustulosa) In this 34-year-old female patient, single, recurrent red papules and pustules have been present on the nose, cheeks and chin for about 4 years.

Amyloidosis systemic of the Al type: in relapses, more prominent after physical exertion, completely asymptomatic, permanently persistent purpura on both lower legs in a 65-year-old. Known plasmocytoma.

Mixed connective tissue disease: 43-year-old female patient (with clinical aspect of systemic lupus erythematosus) who fulfils the criteria of MCTD: U1.nRNP : titre : >1:1600; characteristics of systemic lupus erythematosus, Raynaud's phenomenon, swollen hands as well as feeling ill, fatigue, proximal muscle weakness (typical myositis symptoms).

Klippel-Trénaunay syndrome: extensive vascular malformation with extensive nevus flammeus affecting the trunk and both arms. no evidence of soft tissue hypertrophy so far. no AV fistulas. here detailed picture of the back of the right hand

Purpura jaune d'ocre: multiple, chronically stationary, on the distal lower legs localized, proximally isolated, distally confluent, blurred, symptom-free, light to dark brown, rough, scaling to varying degrees; detectable chronic venous insufficiency (CVI).