Gougerot–Blum syndrome
| Gougerot–Blum syndrome | |
|---|---|
| Other names | Pigmented purpuric lichenoid dermatitis, and Pigmented purpuric lichenoid dermatitis of Gougerot and Blum |
| Pigmented purpuric lichenoid dermatitis of Gougerot and Blum | |
| Specialty | Dermatology |
| Named after |
|
Gougerot–Blum syndrome is a variant of pigmented purpuric dermatitis, a skin condition characterized by minute, rust-colored to violaceous, lichenoid papules that tend to fuse into plaques of various hues.: 829 Relative to other variants, it is characterized clinically by a male predominance, pruritus, with a predilection for the legs, and histologically, it features a densely cellular lichenoid infiltrate.
It was characterized in 1925.
Gougerot–Blum syndrome is named after the French dermatologists Henri Gougerot (1881–1955) and Paul Blum (1878–1933).