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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There may be overlapping characteristics among pigmented purpuric dermatosis and between their signs and those of other purpuric eruptions.
Mayo Clinic Marketplace Check out these best-sellers and special offers on books and newsletters from Mayo Clinic. When blood vessels get inflamed, they can bleed into the skin, causing a reddish-purple rash purpura.
Henoch-Schonlein purpura – Symptoms and causes – Mayo Clinic
See your doctor if you have Henoch-Schonlein purpura and it’s causing serious problems with your digestive tract. Get free access to newly published articles.
Retrieved from ” https: Henoch-Schonlein purpura can ed anyone. You can help Wikipedia by expanding it. Dyschromatosis symmetrica hereditaria Dyschromatosis universalis hereditaria. Argyria Chrysiasis Arsenic poisoning Lead poisoning Titanium metallic discoloration. Infectious triggers may include chickenpox, strep throat, measles and hepatitis.
Other triggers may include certain medications, food, insect bites or exposure to cold weather. Incontinentia pigmenti Scratch dermatitis Shiitake mushroom dermatitis.
HONselect – Pigmentation Disorders
Advertising scnamberg supports our not-for-profit mission. Management of Henoch-Schonlein purpura. Views Read Edit View history. Sign in to download free article PDFs Sign in to access your subscriptions Sign in to your personal account.
Pigmented purpuric dermatosis
Medical care is generally needed if the disorder affects the kidneys. Create a free personal account to make a comment, download free article PDFs, sign up for alerts and more. Sign in to customize your interests Sign in to your personal account.
The condition usually improves on its own. Piebaldism Waardenburg syndrome Tietz syndrome. Nevus depigmentosus Postinflammatory hypopigmentation Pityriasis alba Schambert leukomelanoderma Yemenite deaf-blind hypopigmentation syndrome Wende—Bauckus syndrome.
Disseminated Pruriginous Angiodermatitis (Itching Purpura)
It runs a subacute course and recurrences are not infrequent. But it’s most common in children between the ages of 2 and 6.
Accessed May 18, Ferri’s Clinical Advisor Request an Appointment at Mayo Clinic. 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.
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