Image diagnoses for "skin-colored"
277 results with 598 images

Mycosis fungoides follikulotrope: generalized clinical picture; for about 8 weeks massive painless lymph node swelling on the right side subementally.

Pronounced livedo racemosa: Intermediate findings after 2 more years (period of clinical follow-up over a period of 8 years); extensive scar healing after therapy with high-dose venous immunoglobulin therapy (IVIG)

Herpes simplex virus infection:. grouped standing, crystal clear, shiny vesicles; no central nabekung is visible.

Syringome disseminated: very discreet, skin-coloured, completely symptomless, only cosmetically disturbing nodules in the eyelid area.

Lymphedema, secondary: acutely occurring bulging of the penis in erysipelas.

Necrobiosis lipoidica: Necrobiosis lipoidica that has existed for several years. Large, atrophic scarring (translucent vessels) in the centre. Reddened progression zone at the edges.

Scleroderma, systemic: taut, shiny facial skin (see chin region); distinct perioral fibrosis, which becomes clearly visible when the lips are tapered.

Chronic lymphoedema with positive Stemmer's sign. Massive indurative swelling of the back of the toes with bulging transverse wrinkles.

Lymph cysts with lymphorrhoea in chronic lymphedema of the vulva.

Gynaecomastia: pronouncedbilateral enlargement of the mammae in a 72-year-old male patient; marked obesity.

Lipoma: A subcutaneous lump which has existed for years, is completely unattractive and asymptomatic, can be easily defined and is movable above the underlying tissue and which has developed after an upper abdominal operation.

Atrophy of the skin: age-related flabby atrophy of the dorsal skin with partly swirled, partly parallel, vertical wrinkles; no significant light aging

Light aging of the skin: smooth atrophic skin with flat actinic keratosis (frontal area) with translucent vessels

Lymphedema: one-sided, skin-coloured swelling due to insufficient transport capacity of the lymph vessel system.

Gout tophi: non-inflammatory gout on themetatarsophalangeal joint of the big toe and the back of the foot.

Circumscripts of scleroderma (type Hemiatrophia faciei - Parry-Romberg): Circumscribed, light brown, centrally partly depigmented, porcelain-like shining, non-displaceable substance defect mandibular left. Miniaturized, partly completely atrophic hair follicles and atrophic musculature.
 

Molluscum contagiosum: extensive findings in cases of known immunodeficiency.

Lipomas: spherical soft painless tumours, no longer growing.

Acne conglobata: symmetrically distributed, eminently chronic, inflammatory and melting papules and pustules as well as strong, retracted scar formation, with retention fluctuating in places.

Dorsal cyst, mucoid: painless, approximately 1.0 cm large, skin-coloured, plump, elastic, surface-smooth "nodule" (cyst) which has existed for about 1 year and from which a gelatinous substance has been evacuated at the proximal end (crust-covered part) under pressure, whereby the whole nodule has disappeared. As shown here, a pressure-induced groove-shaped nail dystrophy may occur in the case of longer existing "dorsal cysts".

Small papular type of Mullusca contagiosa: focal sowing of small papular skin-coloured, smooth efflorescences reminiscent of verrucae planae juveniles; isomorphic irritant effect detectable.

Zoster oticus (Ramsay-Hunt Syndrome): pronounced right-sided facial nerve palsy lasting about 3/4 years as a complication of zoster oticus; release of the present illustration by Dr. Martin Hermans, MD.

pachydermoperiostosis, primary: A 32-year-old man of Han Chinese origin presented with a 15-year history of a peculiar facial appearance (Panel A). after puberty, he had noticed a progressive enlargement of his hands and feet as well as facial furrowing. the patient reported that the progression of disease had stabilized by the time he was 27 years of age. on examination, he had excessive sebaceous secretions and thick, furrowed, and redundant skin on his forehead, cheeks, and chinese. soft-tissue hypertrophy reduced the motion of his hands and feet, with terminal broadening of the fingers (Panel B) and toes and cylindrical enlargement of the limbs. the patient received a clinical diagnosis of pachydermoperiostosis, a rare genetic disease characterized by pachyderma, digital clubbing, and periostosis. his parents and son did not have similar symptoms; no genetic testing was performed. the therapy was performed in two stages. in the first stage, we implanted an expander under the patient's forehead skin to enlarg

Congenital fibrolipomatous hamartoma of the calcaneus: congenital soft bulge of the skin, Figure taken from: Yang JH et al (2011) Precalcaneal congenital fibrolipomatous hamartoma Ann Dermatol 23:92-94.

Calcinosis metastatica (detail): Symmetrical, stelae linearly arranged, moderately painful, hard, skin-coloured papules and plaques.