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Primary cutaneous amyloidosis
rareCutaneous amyloidosis refers to a variety of skin diseases characterized histologically by the extracellular accumulation of amyloid deposits in the dermis. Rare forms include lichen amyloidosus, X-linked reticulate pigmentary disorder, primary localized cutaneous nodular amyloidosis, and macular amyloidosis.
- Identifiers
- MONDO:0015301 Orphanet:137807
- Part of
- AmyloidosisDermis disorder
- Also known as
- amyloidosis familial cutaneous lichen · amyloidosis IX · amyloidosis, primary localised cutaneous · lichen amyloidosis familial · primary localised cutaneous amyloidosis
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.