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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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Pigmented purpuric dermatosis

Create a personal account to register for email alerts with links to free full-text articles. A few very small non-blinded studies of treatment with ce ultraviolet light have been reported as promising. Sign in to access your subscriptions Sign in to your personal account.

Purchase access Subscribe to the journal. Pigmented purpuric dermatosis also known as “progressive pigmentary dermatosis,” “purpura pigmentosa chronica,” “pigmentary purpuric eruptions,” or “progressive pigmenting purpura” or “Schamberg’s disease” refers to one of the three major classes of skin conditions characterized by purpuric skin eruptions.

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From Wikipedia, the free encyclopedia. Mayo Clinic Marketplace Check out these best-sellers and special offers on books and newsletters from Mayo Clinic. Its etiopathogenesis is as yet unknown. Disseminated Pruriginous Angiodermatitis Itching Purpura.

In other projects Wikimedia Commons. Retrieved from ” https: Skin color Skin whitening Tanning Sunless. Interventions for preventing and treating scnamberg disease in Henoch-Schonlein purpura. There may be overlapping characteristics among pigmented purpuric dermatosis and enfermedd their signs and those of other purpuric eruptions.

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

Retrieved 22 May enfremedad Oculocutaneous albinism Ocular albinism. But it’s most common in children between the ages of 2 and 6.

Acanthosis nigricans Freckle Familial progressive hyperpigmentation Pallister—Killian syndrome Periorbital hyperpigmentation Photoleukomelanodermatitis of Kobori Postinflammatory hyperpigmentation Transient neonatal pustular melanosis. By using this site, you agree to the Terms of Use and Privacy Policy.

Infobox enfsrmedad condition new All stub articles. Purchase access Subscribe to JN Learning for one year. Related Protein in urine Nausea and vomiting Abdominal pain.

The fundamental clinical characteristics of this condition, which stands out from the rest 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. Sign in to download free article PDFs Sign in to access your subscriptions Sign scuamberg to your personal account. Henoch-Schonlein purpura is an inflammation of the small blood vessels of the skin, joints, bowels and kidneys.


Dee 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.

Clinical manifestations and diagnosis of Henoch-Schonlein purpura.

HONselect – Pigmentation Disorders

When blood vessels get inflamed, they can bleed into the skin, causing a reddish-purple rash purpura. Advertising revenue supports our not-for-profit mission.

Kliegman RM, et al. Vascular-related cutaneous conditions Cutaneous condition stubs.

Henoch-Schonlein purpura – Symptoms and causes – Mayo Clinic

Other triggers may include certain medications, food, insect bites or exposure to cold weather. 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.

It may be the result of the immune system responding inappropriately to certain triggers.

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