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Blue nevus D22.-
Blue nevus: Large blue nevus (so-called Mongolian spot) with a deep dark melanocytic nevus.
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Mononucleosis infectious B27.9
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Mastocytosis (overview) Q82.2
Urticaria pigmentosa adultorum: Classical form of cutaneous mastocytosis (excess of mast cells in the skin) with multiple red patches and wheals (positive Darier sign, due to the friction of the trousers) clearly protruding in the buttock area, and light brown in the adjacent lumbar area, 0.1-0.3 cm in size.
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Lupus erythematosus subacute-cutaneous L93.1
Lupus erythematosus, subacute-cutaneous. Within a few months developing, light-emphasized exanthema with multi-forms and large plaques. No feeling of illness. High titre SSA-Ac.
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Atrophodermia idiopathica et progressiva L90.3
Atrophodermia idiopathica et progressiva: Confluent brownish foci with a central whitish sclerosed area.
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Anticonvulsant hypersensitivity syndrome T88.7
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Mastocytosis (overview) Q82.2
Mastocytosis of the urticaria pigmentosa type: generalised infestation of the integument with disseminated brown spots, patches, papules and plaques, which in some places congregate to form larger areas
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Solar dermatitis L55.-
Dermatitis solaris. almost universal, succulent erythema in a 30-year-old patient (skin type II) after intensive, several hours of sunbathing in the midday sun. accompanying strong sensation of heat, chills and circulatory weakness about 7 hours after exposure to the sun.
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Maculopapular cutaneous mastocytosis Q82.2
Urticaria pigmentosa: Generalized, macular, livid-red to brownish, partly confluent "exanthem-like" clinical picture on the trunk of a 41-year-old woman.
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Mycosis fungoides C84.0
Mycosis fungoides: Plaque stage. 32-year-old male with multiple, disseminated, 1.0-5.0 cm large, moderately itchy, hardly consistency increased, red, rough plaques; clinically and histologically no detectable LK infection.
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Purpura pigmentosa progressive L81.7
Purpura pigmentosa progressiva. discrete blurred red to red-brown spots. slight itching. occurs after taking ibuprofen due to a flu-like infection.
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Nappes claires C84.4
Nappes claires: almost erythrodermic poicolodermatic form of Mycosis fungoides, splashes of light skin in the large mycotic plaques.
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Klippel-trénaunay syndrome Q87.2
Klippel-Trénaunay syndrome. Extensive nevus flammeus; so far no evidence of soft tissue hypertrophy. No pelvic obliquity!
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Phototoxic dermatitis L56.0
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Neurofibromatosis (overview) Q85.0
Neurofibromatosis segmental, type V Neurofibromatosis. Unilaterally distributed café au lait stains.
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Mosaic cutaneous
Mosaic cutaneous(Hypomelanosis Ito): congenital fernlike depigmentation of the skin, no symptoms.