
Nevus of Ota D22.30
Naevus fuscocoeruleus ophthalmomaxillaris. Irregularly limited, planar, brown to blackish blue, half-sided pigmentation. No clinical symptoms.

Erythema perstans faciei L53.83
Erythema perstans faciei. persistent, butterfly-shaped, livid red erythema in a 3-year-old boy with vitium cordis (pulmonary stenosis, subaortic stenosis, vascular transport and ventricular septal defect).

Crest syndrome M34.1
Crest syndrome,numerous telangiectases, sclerosis of the facial skin, periorbital radial wrinkles.

Rosacea L71.1; L71.8; L71.9;
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.

Rosacea L71.1; L71.8; L71.9;
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.

Erythema perstans faciei L53.83
Erythema perstans faciei: symmetrical, changing redness of both cheeks (here circled) Fixed erythema on chin and cheeks marked with arrows.

Scleroderma systemic M34.0
Scleroderma, systemic: within 2-3 years, newly developed telangiectasia of the facial skin.

Angiosarcoma of the head and face skin C44.-

Argyria L81.8
Argyrie: diffuse, grey to grey-brownish, metallically shiny, diffuse discolouration of the facial skin due to deposition of silver complexes.

Erythema perstans faciei L53.83
erythema perstans faciei. persistent, asymptomatic, symmetrically arranged facial redness. no other diseases known.

Melasma L81.1
Chloasma/melasma ina 27-year-old Ethiopian female patient after prolonged use of oral anticonceptives; large, bizarrely bordered hyperpigmentation of the cheek, lips, nose and forehead.

Teleangiectasia I78.8
Teleangiectasia. Reticularly branched, irregular vascular dilatations in the cheek area.

Erythema infectiosum B08.30
erythema infectiosum. after slight "flu-like" infection intensive redness (and swelling) of both cheeks (cheek whistle face). 2 days later little symptomatic exanthema with anular erythema on the arms. cervical lymphadenopathy. laboratory: o.B.

Melanodermatitis toxica L81.4
Melanodermatitis toxica. solitary, chronically stationary (no growth dynamics), large-area, blurred, symptom-free (only cosmetically disturbing), brown, smooth spot in an obese, 63-year-old patient of Turkish origin. in addition, multiple follicular keratoses are visible in the zygomatic bone region and periorbital right side.

Vitiligo (overview) L80

Chronic actinic dermatitis (overview) L57.1
Dermatitis chronic actinic (type light-provoked atopic eczema). general view: Disseminated, scratched papules and plaques, nodular in places, as well as blurred, large-area, reddened, severely itching erythema on the face of a 51-year-old female patient with atopic eczema existing since birth. the skin changes can be provoked by sunlight and photopatch testing.

Teleangiectasia I78.8
Teleangiectasia. Harm sleeve, reticularly branched, irregular vascular dilatations in the area of both cheeks.

Porphyria cutanea tarda E80.1
Porphyria cutanea tarda: dirty brown hyperpigmentation; hypertrichosis in the area of the temple and cheek.

Acrocyanosis I73.81; R23.0;
acrocyanosis in right heart failure. extensive homogeneous reddening of the facial areas. clearly more prominent in cold weather. moderate cyanosis of the red of the lips. age involution of the chin region with oblique chin furrows. moist corners of the lips with occasional pearlèche.