Apolipoprotein C-II Deposition Amyloidosis: A Potential Misdiagnosis as Light Chain Amyloidosis

Hereditary amyloidoses are rare and pose a diagnostic challenge. We report a case of hereditary amyloidosis associated with apolipoprotein C-II deposition in a 61-year-old female presenting with renal failure and nephrotic syndrome misdiagnosed as light chain amyloidosis. Renal biopsy was consistent...

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Bibliografski detalji
Izdano u:Case Rep Nephrol
Glavni autori: Lohani, Sadichhya, Schuiteman, Emily, Garg, Lohit, Yadav, Dhiraj, Zarouk, Sami
Format: Artigo
Jezik:Inglês
Izdano: Hindawi Publishing Corporation 2016
Teme:
Case Report
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5093243/
https://ncbi.nlm.nih.gov/pubmed/27840752
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/8690642
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