Letters to the Editor
AA amyloidosis as a rare presentation leading to the diagnosis of mevalonate kinase deficiency in a male adult: a diagnostic challenge mimicking familial Mediterranean fever
A.C. Pozzi1, G. Voltarel2, P. Airo'3, M. Frassi4, I. Cavazzana5, F. Crisafulli6
- Rheumatology and Clinical Immunology Unit, ERN ReCONNET, ASST Spedali Civili of Brescia; and Department of Clinical and Experimental Sciences, University of Brescia, Italy.
- Rheumatology and Clinical Immunology Unit, ERN ReCONNET, ASST Spedali Civili of Brescia; and Department of Clinical and Experimental Sciences, University of Brescia, Italy.
- Rheumatology and Clinical Immunology Unit, ERN ReCONNET, ASST Spedali Civili of Brescia; and Department of Clinical and Experimental Sciences, University of Brescia, Italy.
- Rheumatology and Clinical Immunology Unit, ERN ReCONNET, ASST Spedali Civili of Brescia; and Department of Clinical and Experimental Sciences, University of Brescia, Italy.
- Rheumatology and Clinical Immunology Unit, ERN ReCONNET, ASST Spedali Civili of Brescia; and Department of Clinical and Experimental Sciences, University of Brescia, Italy.
- Rheumatology and Clinical Immunology Unit, ERN ReCONNET, ASST Spedali Civili of Brescia; and Department of Clinical and Experimental Sciences, University of Brescia, Italy. crisafulli.francesca10@gmail.com
CER19978
Letters to the Editor
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PMID: 42873706 [PubMed]
Received: 30/03/2026
Accepted : 08/05/2026
In Press: 09/10/2026
