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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Dades bibliogràfiques
Publicat a:Case Rep Nephrol
Autors principals: Lohani, Sadichhya, Schuiteman, Emily, Garg, Lohit, Yadav, Dhiraj, Zarouk, Sami
Format: Artigo
Idioma:Inglês
Publicat: Hindawi Publishing Corporation 2016
Matèries:
Case Report
Accés en línia: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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