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Saudi J Kidney Dis Transpl ; 31(2): 508-514, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32394925

RESUMO

Amyloidosis has traditionally been of a few defined varieties, most commonly including light-chain amyloidosis (AL amyloidosis) and secondary amyloidosis due to chronic inflammation (AA amyloidosis). Apolipoprotein A-I/A-II cystatin C, gelsolin, lysozyme, fibrinogen alpha chain, beta 2 microglobulin, and transthyretin familial amyloidosis represent rarer but reported varieties. Ten years ago, the first reports linked leukocyte chemotactic factor 2 (LECT2) amyloidosis as a pathological agent identified as a novel class of amyloid-generating protein. Epidemiology suggested that this was a new cause of amyloidosis that is especially common in Hispanic patients and somewhat common among patients from the Middle East-North Africa (MENA) region. We report a case of splenic and renal LECT 2 amyloidosis in a 62-year- old Hispanic male with diabetes mellitus. After an unremarkable serological workup, LECT 2 amyloidosis was diagnosed on renal biopsy. The case presentation is reviewed as a typical presentation, and the literature is reviewed regarding this newly reported entity, resulting in infiltrative renal amyloidosis and chronic renal disease.


Assuntos
Amiloidose/diagnóstico , Rim/química , Insuficiência Renal Crônica/diagnóstico , Esplenopatias/diagnóstico , Amiloidose/metabolismo , Amiloidose/patologia , Amiloidose/terapia , Biomarcadores/análise , Biópsia , Humanos , Peptídeos e Proteínas de Sinalização Intercelular/análise , Rim/ultraestrutura , Masculino , Microscopia Eletrônica , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Insuficiência Renal Crônica/metabolismo , Insuficiência Renal Crônica/patologia , Insuficiência Renal Crônica/terapia , Esplenopatias/metabolismo , Esplenopatias/patologia , Esplenopatias/terapia , Coloração e Rotulagem , Resultado do Tratamento
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