Angiokeratoma of the glans penis. multiple, chronically stationary, 0.2-0.4 cm large, blue-red to brownish papules with partly smooth, partly scaly surface in the area of the corona glandis. these are congenital, circumscribed vascular ectasias.
Mucinosis follicularis: itchy, disseminated, follicular, well-defined, pointed, skin-coloured papules with firmly adhering hyperkeratosis on the back and the lateral thoracic parts; clinical picture of a "grating iron skin".
Acrokeratoelastoidosis: In a band-shaped arrangement at the transition zone from field skin to groin skin lichenoid shiny, 0.1-0.2 cm large, polygonally limited, yellowish to skin-coloured, completely asymptomatic papules appear.
Connective tissue nevus, lumbosacral. 30-year-old woman, in whom these changes had been present since earliest childhood. Clinically, in the sacral region, sharply defined, very firm, partly rubbery, slightly raised above the skin level, cobblestone-like arranged, whitish papules and plaques with smooth surface are found. Localization and clinic are characteristic for the diagnosis. Secondary findings are angiofibromas in the face.
Type I Neurofibromatosis, peripheral type or classic cutaneous form. Since puberty slowly increasing formation of these soft, skin-coloured or slightly brownish, painless papules and nodules. Several café-au-lait spots.
Small papular type of Mullusca contagiosa: focal sowing of small papular skin-coloured, smooth efflorescences reminiscent of verrucae planae juveniles; isomorphic irritant effect detectable.
Syringome disseminated:skin-coloured to slightly brownish, completely asymptomatic, surface-smooth, roundish or elongated, broad-based nodules locatedon thetrunk and in the facial region.
Mucinosis follicularis: acute clinical picture developed after heavy sweating; multiple, generalised, 0.1 cm large, itchy, skin-coloured, pointed conical, rough papules bound to follicles.
Basal cell carcinoma, nodular. 2.5 years of persistent, slowly growing, now 1.8 x 2.3 cm large, centrally ulcerated tumor with telangiectasias in the lower border wall at the right nasolabial fold of a 69-year-old patient.
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