AL amyloidosis (Q40143): Difference between revisions

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+August 2026Timestamp +2026-08-13T00:00:00Z
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@@ Property / Collection date: 13 August 2026 / rank @@
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+E85.8
@@ Property / Linked ICD 10: E85.8 / rank @@
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Latest revision as of 05:50, 13 August 2026

AL (Amyloid Light-Chain) Amyloidosis is due to the deposition of immunoglobulin light chains in glomeruli where they are seen as Congo red binding fibrils and immuno-stain specifically for kappa or lambda light chains. By light microscopy there is amorphous hyaline material in the mesangium and capillary walls. A light chain producing plasma cell or B-cell dysplasia is responsible. Other organs are also involved in this systemic disease.

Language	Label	Description	Also known as
default for all languages	5D00.0
English	AL amyloidosis	AL (Amyloid Light-Chain) Amyloidosis is due to the deposition of immunoglobulin light chains in glomeruli where they are seen as Congo red binding fibrils and immuno-stain specifically for kappa or lambda light chains. By light microscopy there is amorphous hyaline material in the mesangium and capillary walls. A light chain producing plasma cell or B-cell dysplasia is responsible. Other organs are also involved in this systemic disease.