Results: 6

Granulomatous pigmented purpuric dermatosis: report of a Latin-American case with blaschkoid distribution

An. bras. dermatol; 94 (5), 2019
Abstract Granulomatous pigmented purpuric dermatosis clinically manifests as hyperpigmented maculae and petechiae, predominantly on the lower extremities. Histopathologically, it is characterized by a lymphocytic infiltrate in the upper dermis, extravasated erythrocytes, and hemosiderin deposits. There i...

Pigmented purpura and cutaneous vascular occlusion syndromes

An. bras. dermatol; 93 (3), 2018
Abstract: Purpura is defined as a visible hemorrhage in the skin or mucosa, which is not evanescent upon pressure. Proper classification allows a better patient approach due to its multiple diagnoses. Purpuras can be categorized by size, morphology, and other characteristics. The course varies according ...

Schamberg's disease: case report with therapeutic success by using colchicine

An. bras. dermatol; 92 (2), 2017
Abstract: Pigmented purpuric dermatoses (PPD) include a spectrum of diseases with different clinical aspects, but with similar histopathological features. Specific clinical findings allow the division of PPD in variants. Schamberg's disease is the most common. Treatment is sometimes ineffective and recur...

Dermatoscopic findings of pigmented purpuric dermatosis

An. bras. dermatol; 91 (5), 2016
Abstract: Background: Pigmented purpuric dermatosis is a chronic skin disorder of unknown aetiology characterised by symmetrical petechial and pigmented macules, often confined to the lower limbs. The aetiology of pigmented purpuric dermatosis is unknown. Dermatoscopy is a non-invasive diagnostic techni...

Cocaine/levamisole-induced systemic vasculitis with retiform purpura and pauci-immune glomerulonephritis

Braz. j. med. biol. res; 49 (5), 2016
Levamisole has been increasingly used as an adulterant of cocaine in recent years, emerging as a public health challenge worldwide. Levamisole-associated toxicity manifests clinically as a systemic vasculitis, consisting of cutaneous, hematological, and renal lesions, among others. Purpura retiform, cuta...

Dermatosis purpúrica pigmentaria, variante granulomatosa, a propósito de un caso
Granulomatous variant of chronic pigmented purpuric dermatosis: case report

Rev. chil. dermatol; 32 (1), 2016
La dermatosis purpúrica pigmentaria (DPP) corresponde a un grupo de enfermedades caracterizadas clínicamente por petequias y coloración bronce de la piel. Generalmente se localiza en las extremidades inferiores y se describen varios tipos, dentro de los cuales se encuentra la variante granulomatosa. S...