Image diagnoses for "brown"
372 results with 1434 images
Results forbrown

Parry Romberg syndrome G51.8
Hemiatrophia faciei progressiva: Fig. 1 Initial documentation of the hemifacial atrophy.

Hyperpigmentation L81.89
Physiological tanning by solarium, reduced pigmentation at the contact points.

Extrinsic skin aging L98.8
Chronic light damage: poikiloderma after years of excessive UV exposure, including hyperpigmentation, depigmentation and numerous precanceroses of the actinic keratosis type.

Acanthosis nigricans (overview) L83
Acanthosis nigricans: Bilateral greyish-brown, papillomatous-hyperkeratotic, asymptomatic, flat, rough plaques in a 40-year-old obese African-American patient.

Sarcoidosis of the skin D86.3
Sarcoidosis plaque form: 5.0 cm large, coarse lamellar scaling, reddish-brown plaque, existing for several years, without symptoms, detailed view.

Nevus verrucosus Q82.5
Naevus verrucosus with bizarre arrangement of brownish papules and plaques along the Blaschko lines.

Kaposi's sarcoma (overview) C46.-
Kaposi's sarcoma epidemic (overview): HIV-associated Kaposi's sarcoma with disseminated, bizarrely configured, reddish-brown plaques, sometimes in a striped arrangement.

Lentigo maligna melanoma C43.L

Sarcoidosis of the skin D86.3
Sarcoidosis of the skin: slightly pressure-painful, scaly brown plaque of the skin that slides over the underlay.

Bowen's disease D04.9
Bowen's disease: Sharply bordered brownish plaque that has existed for 2 years, is completely asymptomatic, sharply bordered and brown in colour.

Chloasma gravidarum perstans L81.1

Lichen simplex chronicus L28.0
Lichen simplex chronicus indark skin. several lesions with 0.1-0.2 cm large, marginally disseminated, firm brown-black papules confluent in the centre of the lesions. permanent itching.

Lymphomatoids papulose C86.6
Lymphomatoid papulosis: chronic, relapsing, completely asymptomatic clinical picture with multiple, 0.3 - 1.2 cm large, flat, scaly papules and nodules as well as ulcers. 35-year-old otherwise healthy man.

Neurofibromatosis (overview) Q85.0
Type I Neurofibromatosis, peripheral type or classic cutaneous form Peripheral neurofibromatosis with multiple skin-coloured to light brown, soft nodes and nodules, sometimes also stalked, bulging soft, skin-coloured dewlap on the left hip.

Hyperpigmentation postinflammatory L81.0

Keratosis areolae mammae naeviformis Q82.5
Keratosis areolae mammae naeviformis: Chronic stationary plaque in a 45-year-old man, unchanged for years, limited to the nipple and areola, moderately increased in consistency, without symptoms, brown, rough (warty) plaque.