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Gougerot–Blum syndrome (also known as "Pigmented purpuric lichenoid dermatitis," and "Pigmented purpuric lichenoid dermatitis of Gougerot and Blum"〔) 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. 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.〔Barnhill RL and Crowson AN (eds) Textbook of Dermatopathology, second edition, McGraw-Hill, 2004: 211-212〕 It was characterized in 1925. == See also == * Pigmentary purpuric eruptions * Skin lesion * List of cutaneous conditions 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Gougerot–Blum syndrome」の詳細全文を読む スポンサード リンク
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