Papular amyloidosis (Q106242): Difference between revisions
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16 August 2026
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Latest revision as of 13:04, 17 August 2026
Papular amyloidosis (lichen amyloidosis) presents as multiple discrete, firm, pruritic, skin-coloured or hyperpigmented papules which have a tendency to coalesce into plaques. These are located most commonly on the shins though the thighs and upper extremities may also be affected. The amyloid material is thought to originate from degenerate keratinocytes. Papular amyloidosis tends to be persistent and resistant to treatment.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1889504911 |
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| English | Papular amyloidosis |
Papular amyloidosis (lichen amyloidosis) presents as multiple discrete, firm, pruritic, skin-coloured or hyperpigmented papules which have a tendency to coalesce into plaques. These are located most commonly on the shins though the thighs and upper extremities may also be affected. The amyloid material is thought to originate from degenerate keratinocytes. Papular amyloidosis tends to be persistent and resistant to treatment. |
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CID11:ID_1889504911
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dki-india-ID_1889504911
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Concluído
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16 August 2026
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