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A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Pigmented. Barnatán, M., and Casalá, A. M.: Dos casos de enfermedad de Schamberg generalizada, Arch Argent Derm , 3. Doucas, C., and Kapetanakis, . in Schamberg’s disease. Finzi15 have . simulate those of Schamberg’s disease. The lower limbs are enfermedad de Schamberg generalizada, Arch Argent.

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Mayo Clinic Marketplace Check out these best-sellers and special offers on books and newsletters from Mayo Clinic. The fundamental clinical characteristics of this condition, which stands out from the ed of the purpuric and pigmentary dermatitides and which was first observed in many countries slightly over ten years ago, consist of widely disseminated purpuric lesions associated with pruritus.

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From Wikipedia, the free encyclopedia. Albinism Oculocutaneous albinism Ocular albinism.

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Pigmented purpuric dermatosis

Purchase access Subscribe now. A few very small non-blinded studies of treatment with narrow-band ultraviolet light have been reported as promising. Andrews’ Diseases of the Skin: Although vascular damage may be present, it is insufficient for these conditions to be considered forms of vasculitis. As a contribution towards its knowledge, we have reviewed the literature and described the symptomatology and treatment, and we suggest its inclusion as a separate entity among the conditions which bear the generic name of angiodermatitis.

Why this initial inflammation develops isn’t clear.

HONselect – Pigmentation Disorders

But it’s most common in children between the ages of 2 and 6. Create a free personal account to download free article PDFs, sign up for alerts, customize your interests, and more. Sign in to make a comment Sign in to your personal account.

Acanthosis nigricans Freckle Familial progressive hyperpigmentation Pallister—Killian syndrome Periorbital hyperpigmentation Photoleukomelanodermatitis of Kobori Postinflammatory hyperpigmentation Transient neonatal pustular melanosis. Alezzandrini syndrome Vogt—Koyanagi—Harada syndrome.

Accessed May 18, D ICD – This cutaneous condition article is a stub. Dyschromatosis symmetrica hereditaria Dyschromatosis universalis hereditaria. Dermatopathia pigmentosa reticularis Pigmentatio reticularis faciei et colli Reticulate acropigmentation of Kitamura Reticular pigmented anomaly of the flexures Naegeli—Franceschetti—Jadassohn syndrome Dyskeratosis congenita X-linked reticulate pigmentary disorder Galli—Galli disease Revesz syndrome.


Argyria Chrysiasis Arsenic poisoning Lead poisoning Titanium metallic discoloration. Rarely serious kidney damage can occur. By using this site, you agree to the Terms of Use and Privacy Policy. Sign in to customize your interests Sign in to your personal account. Create a free personal account to access your subscriptions, sign up for alerts, and more.

In Henoch-Schonlein purpura, some of the body’s small blood vessels become inflamed, which can cause bleeding in the skin, abdomen and kidneys.

Views Read Edit View history. Henoch-Schonlein purpura can affect anyone. Create a zchamberg account to register for email alerts with links to free full-text articles. Pigmented purpuric dermatosis are distinguished from other purpura by size 0. For most people, symptoms improve within a month, leaving no lasting problems.

Skin color Skin whitening Tanning Sunless.