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A Case of Severe Cholestasis due to Hepatic AL Amyloidosis
INTRODUCTION: Immunoglobulin light chain-associated amyloidosis results from extracellular tissue deposition of fibril-forming monoclonal immunoglobulin light chains, secreted by a clone of plasma cells. Although the liver is often involved histologically, most cases are clinically asymptomatic, and...
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| Vydáno v: | GE Port J Gastroenterol |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
S. Karger AG
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6876644/ https://ncbi.nlm.nih.gov/pubmed/31832498 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000496185 |
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