• Skip to primary navigation
  • Skip to main content
BC

biochimica clinica

en_US English
en_US English it_IT Italian

CASI CLINICI – Case Reports

Volume:

Biochimica Clinica 2016; 40(2) e12-e15

Published on-line:

April 26, 2016

DOI:

10.19186/BC_2016.005

Download in PDF:

Utilità del saggio Hevylite nella gestione clinica di una paziente affetta da amiloidosi AL con gammopatia biclonale

AUTHORS

Veronica Valentini1, Francesca Lavatelli1, Paolo Milani1, Francesca Russo1, Marco Basset1, Tiziana Bosoni2, Laura Pirolini2, Filomena Li Bergolis2, Gabriele Sarais2, Giovanni Palladini1, Giampaolo Merlini1,2
1Centro per lo Studio e la Cura delle Amiloidosi Sistemiche, Fondazione IRCCS Policlinico San Matteo, Pavia e Dipartimento di Medicina Molecolare, Università degli Studi di Pavia
2Laboratorio Analisi-Chimico-Cliniche, Fondazione IRCCS Policlinico San Matteo, Pavia

Questo lavoro è stato in parte presentato al 46° Congresso Nazionale SIBioC, 13-15 Ottobre 2014, Roma, all'interno della Sessione "Casi clinici indimenticabili: il contributo della Medicina di Laboratorio".

ABSTRACT

Usefulness of the Hevylite assay in the management of a patient with AL amyloidosis and biclonal gammopathy

Patients with AL amyloidosis often have small monoclonal components (MCs) difficult to quantify by densitometry. IgA are the most problematic, due to anodic migration and possible masking under proteins migrating in β zone. We evaluated the usefulness of the Hevylite assay (Binding Site, Birmingham UK), at diagnosis and during follow-up, in a patient with AL amyloidosis and biclonal gammopathy. At diagnosis serum immunofixation identified an IgGλ and an IgAλ band (the last one not reliably quantifiable in capillary electrophoresis). The κ serum free light chain (FLC) concentration was 4.94 mg/L and λ 26 mg/L (κ/λ ratio 0.19). The Hevylite test showed both IgGλ and IgAλ above the reference limits, with abnormal κ/λ ratios. After treatment, a 27% decrease in IgGλ and a 56% decrease in IgAλ concentration were documented by Hevylite, which was the only mean to quantify the monoclonal components in this patient.

REFERENCES