prurigo การใช้

• In 1971, Nagashima reported a peculiar pruritic dermatosis he designated Prurigo pigmentosa.
• It is sometimes considered to be a term encompassing Besnier prurigo and other conditions.
• The most common prurigo simplex symptoms are skin nodules resembling insect bites that are intensely itchy.
• Prurigo simplex is a pruritus disorder of the skin characterized by extremely itchy skin nodules and lesions.
• The eponymous Besnier's prurigo is named for a skin disorder that often follows infantile atopic dermatitis.
• Rarely it may represent a genetic susceptibility to light damage ( e . g . xeroderma pigmentosum or actinic prurigo ).
• "' Actinic prurigo "'is a common sunlight-induced, pruritic, papular or nodular skin eruption.
• Typically, there is no known direct cause of prurigo simplex, but some factors are known to trigger or aggravate it.
• Prurigo pigmentosa is a rare skin condition of unknown cause that affects depressed places on the chest and back like the intermammary area.
• Was a Japanese dermatologist, the first professor of dermatology at Kyorin University, who proposed the designation of " Prurigo pigmentosa ".
• In 1808 he obtained his medical doctorate in Paris with the thesis " " Dissertation sur une maladie de la peau d閟ign閑 sous le nom de prurigo " ".
• Some experts use the term " actinic prurigo " for Hutchinson's summer prurigo ( aka " hydroa aestivale " ) and several other photodermatoses that might, or might not, be distinct clinical entities.
• Some experts use the term " actinic prurigo " for Hutchinson's summer prurigo ( aka " hydroa aestivale " ) and several other photodermatoses that might, or might not, be distinct clinical entities.
• Some patients may show erythema or severe pruritus alone, wheals of chronic urticaria, purpuric lesions resembling petechiae on hands and feet, palmo-plantar keratosis, leukocytoclastic vasculitis-like appearance, and / or lesions mimicking prurigo pigmentosa.
• Some medical experts use the term " actinic prurigo " to denote a rare photodermatosis that develops in childhood and is chronic and persistent; this rare photodermatosis, associated with the human leukocyte antigen HLA-DR4, is often called " Familial polymorphous light eruption of American Indians " or " Hereditary polymorphous light eruption of American Indians " but some experts consider it to be a variant of the syndrome known as polymorphous light eruption ( PMLE ).