Papular amyloidosis (Q106242): Difference between revisions

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A amiloidose papular (líquen amiloide) apresenta-se como múltiplas pápulas discretas, firmes, pruriginosas, da cor da pele ou hiperpigmentadas que têm tendência a coalescer em placas. Localizam-se mais comumente nas canelas, embora as coxas e as extremidades superiores também possam ser afetadas. Acredita-se que o material amilóide se origine de queratinócitos degenerados. A amiloidose papular tende a ser persistente e resistente ao tratamento.
description / endescription / en
 
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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Property / Canonical URI: https://id.who.int/icd/entity/1889504911 / rank
 
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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
Timestamp+2026-08-16T00:00:00Z
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CalendarGregorian
Precision1 day
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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.
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    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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