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Systemic amyloidosis
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Primary systemic amyloidosis(AL> > AH amyloid protein)
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Plasma cell dyscrasias (more common)
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Multiple myeloma-associated
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Secondary systemic amyloidosis (reactive;AA amyloid protein)
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Chronic inflammation (e.g.rheumatoid arthritis)
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Chronic infection (e.g.tuberculosis)
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Heredofamilial amyloidosis (various amyloid proteins)
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Familial amyloidotic polyneuropathy
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Familial Mediterranean fever
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Organ-limited (localized)amyloidosis
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Cutaneous
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Primary:macular, lichen, biphasic, dyschromic, nodular
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Secondary:within skin tumors
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Endocrine
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Medullary carcinoma of the thyroid, insulinoma, type 2 diabetes
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Cerebral
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Alzheimer 's disease
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