| Autor: |
S. Pirasath, T. Kumanan, G. Selvaratnam, V. Sujanitha, D. D. Dikowita |
| Jazyk: |
angličtina |
| Rok vydání: |
2019 |
| Předmět: |
|
| Zdroj: |
Sri Lanka Journal of Medicine, Vol 28, Iss 1, Pp 65-69 (2019) |
| Druh dokumentu: |
article |
| ISSN: |
2579-1990 |
| DOI: |
10.4038/sljm.v28i1.101 |
| Popis: |
SSystemic AL- amyloidosis is a disorder of protein folding in which there is extra-cellular accumulation as β pleated fibrillar deposits of monoclonal immunoglobulin light chain fragments. AL- amyloidosis is a rare clinical entity. A presentation with clinical and histological evidence of gastrointestinal amyloidosis is even rare. Here we report primary AL- amyloidosis secondary to lamda (λ) light chain myeloma in a middle-aged woman who presented with nephrotic syndrome and motor peripheral neuropathy. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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