Image diagnoses for "Macule"
332 results with 1231 images
Results forMacule

Melanotic spots of the mucous membranes L81.4
Lentigo of the mucous membrane: sharply defined, brownish hyperpigmentation of the red of the lips and the lip mucosa.

Psoriasis vulgaris L40.00
psoriasis vulgaris. treated psoriasis vulgaris. the previously existing typical psoriatic plaques are replaced by red spots with marginal hyperpigmentation. the treatment was carried out locally with dithranol [cignolin]. scaling no longer present. the brewing discoloration of the lesional surroundings are reversible discolorations of the nromal skin by diathranol. the diagnosis "psoriasis" is doubtless due to the known anamnesis.

Hypomelanosis ito Q82.3
Incontinentia pigmenti achromians: Mosaic-like hypopigmentations of the left trunk and leg in a 2-year-old girl which appeared for the first time in the 4th month of life and have been progressive since then.

Becker's nevus D22.5
Becker nevus: planar and spatter-like hyperpigmentation, focal hypertrichosis in the region of the lateral thoracic wall in young men; hardly visible at birth, postpubertal expression.

Lentigo maligna melanoma C43.L

Cutis marmorata teleangiectatica congenita Q27.8
Cutis marmorata teleangiectatica congenita (localisata), symptomless vascular malformation with reticular and extensive redness and vascular veins sharply limited to hands and the distal forearm.

Ashy dermatosis L81.02
Erythema dyschromicum perstans. 49-year-old male. Several months old with extensive gray-brown patches on the trunk. No itching. No drug history?

Striated leukonychia L60.8
Dermatoscopy: Periodic, stripe-shaped (since years existing) white coloration of the nail plate in a 50-year-old woman, middle finger.

Acrocyanosis I73.81; R23.0;
Acrocyanosis: A flat, symptomless, blurredly limited, red-livid spot in the buttocks of a 52-year-old woman, which becomes much more prominent when exposed to cold.

Asymmetrical nevus flammeus Q82.5
Vascular (capillary) malformation (so-called naevus flammeus): Congenital, generalized, irregularly configured, spotty erythema from the scalp to the sole of the foot in a 5-year-old boy, developed according to age. Here changes of the sole of the foot.

Nevus anaemicus Q82.5
Naevus anaemicus: Approximately palm-sized, irregularly limited, white, smooth stain. No reddening after rubbing the stain. On glass spatula pressure the borders to the surrounding area disappear.

Atopic dermatitis in children and adolescents L20.8
eczema atopic in childhood: 14-year-old adolescent with generalized atopic eczema. striking grey-brown, dry skin. multiple scratched papules and plaques. extensive, therapy-resistant pyoderma on the left thigh (developed after traumatic abrasion)

Nail diseases (overview) L60.8
Striped onychodystrophy: harmless, age-related striped onychodystrophy with a girdles-like stripe pattern

Vasculitis leukocytoclastic (non-iga-associated) D69.0; M31.0
Vasculitis leukocytoclastic (non-IgA-associated): multiple, since 1 week existing, on both legs symmetrically localized, irregularly distributed, 0.1-0.2 cm large, confluent in places, symptomless, red, smooth spots (not compressible).

Chronic actinic dermatitis (overview) L57.1
Dermatitis, chronic actinic (type actinic reticuloid). large-area, chronically dynamic, severe eczema reaction limited to UV-exposed skin areas with rough, extensive eminently itchy plaques with fine dense scaling. massive actinic elastosis (see deep rhomboidal skin field of the entire face). already after brief exposure to the sun, increase in burning itching. no history of atopy. probably caused by the intake of thiazide-containing diuretics.

Adult dermatomyositis M33.1
dermatomyositis: reflected light microscopy. hyperkeratotic nail folds. pathologically increased and enlarged torqued capillaries. older bleeding into the nail fold.

Purpura thrombocytopenic M31.1; M69.61(Thrombozytopenie)
Thrombocytopenic purpura: colorful picture of a symmetrical, orthostatic purpura with fresh, punctiform, red bleeding.

Purpura thrombocytopenic M31.1; M69.61(Thrombozytopenie)
Purpura thrombocytopenic: acutely occurring, partly large-area, partly punctiform, non-anemic spots with a tendency to confluence; sudden onset with fever, multiple thromboses, disorientation, stupor; it is a drug-induced form of thrombotic thrombocytopenic purpura with hemolytic microangiopathic anemia at the base of an infectious disease and a previously unknown drug allergy.






