How do you get rid of pigmented purpuric dermatosis?
No medical intervention is of consistent benefit for the treatment of the pigmented purpuric dermatoses. Pruritus may be alleviated by the use of topical corticosteroids and antihistamines. Associated venous stasis should be treated by compression hosiery. Prolonged leg dependency should be avoided.
What is Schamberg’s purpura?
Schamberg purpura is the result of leakage of blood from small capillaries in the superficial papillary dermis. The resultant purpura is nonblanching but is not palpable. No pronounced damage occurs to the blood vessel walls, differentiating this condition from vasculitis.
What is lichenoid purpura?
Pigmented purpuric lichenoid dermatitis of Gougerot-Blum (PPLD) is a chronic, relapsing, uncommon benign variant of pigmented purpuric dermatosis (PPD), first described by Gougerot and Blum in 1925. It typically affects middle-aged men, although it may present earlier in life [1, 2].
How do you treat majocchi’s granuloma?
Oral terbinafine has been used worldwide for Majocchi granuloma. The administration of systemic terbinafine for 6 weeks is the best treatment option in a patient with a transplanted kidney and Majocchi granuloma. Oral antifungals are usually necessary because topical agents alone are not effective.
Is schamberg disease fatal?
There is no cure for Schamberg’s disease, however, this condition is not life-threatening or a major health concern. The most usual problems that patients will encounter is discoloration of the skin and, occasionally, itching. Itching may be improved by applying a cortisone cream.
How long does it take purpura to go away?
Most purpuric lesions last between one and three weeks, though the discoloration may be permanent after they fade. You can talk to your dermatologist about how to reduce their appearance.
What does pigmented purpura look like?
The main features of pigmented purpuric dermatosis (PPD) are petechiae (tiny red spots due to broken blood vessels) or purpura (purple-colored spots or patches due to broken blood vessels), and yellow to brown pigmented patches. The most common sites are the legs, although lesions also may develop in other areas.
Is pigmented purpuric dermatosis genetic?
The cause of pigmented purpuric dermatosis is unknown. Occasionally, it occurs as a reaction to a medication, food additive, viral infection or following exercise. In rare cases, there appears to be a genetic component.
What is Gougerot Blum PPLD?
Pigmented purpuric lichenoid dermatitis of Gougerot-Blum (PPLD) is a chronic, relapsing, uncommon benign variant of pigmented purpuric dermatosis (PPD), first described by Gougerot and Blum in 1925. It typically affects middle-aged men, although it may present earlier in life [1, 2].
What is pigmented purpuric lichenoid dermatitis of Gougerot and Blum?
The topic Pigmented Purpuric Lichenoid Dermatitis of Gougerot and Blum you are seeking is a synonym, or alternative name, or is closely related to the medical condition Gougerot-Blum Disease. Gougerot-Blum Disease is a skin condition that manifests as multiple, small papules that form plaques.
What is Gougerot-Blum disease?
Gougerot-Blum Disease is a skin condition that manifests as multiple, small papules that form plaques. These are usually observed in the legs, which then slowly spreads to the rest of the body It is also known as Pigmented Purpuric Lichenoid Dermatitis of Gougerot and Blum and has no known cause.
Is Gougerot-Blum dermatitis related to Schamberg’s disease?
The clinical and histological findings in a case of pigmented purpuric lichenoid dermatitis of Gougerot-Blum is presented, and the relationship of this disease to Schamberg’s disease, Majocchi’s disease, and angioma serpiginosum of Hutchinson is reviewed. Pigmented purpuric lichenoid dermatitis of Gougerot-Blum