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Published in: Rheumatology International 8/2020

01-08-2020 | Vasculitis | Case Based Review

Crystalglobulinemia manifested as acute renal failure and thrombotic vasculopathy

Authors: L. Gómez-Lechón Quirós, M. E. Acosta De La Vega, O. Compán Fernández, S. Pastor Navarro, C. Montilla Morales, D. Moyano Bueno, J. Martín Centellas, A. Santos-Briz Terrón, C. Hidalgo Calleja

Published in: Rheumatology International | Issue 8/2020

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Abstract

Crystalglobulinemia is an extremely rare pathology that is associated in most cases with plasma cell dyscrasia, mainly multiple myeloma. In most cases, it may be the manifestation of incipient gammopathy or it manifests shortly after diagnosis. We report a patient with ischemic lesions of thrombotic origin in lower limbs. Subsequently, renal involvement occurs, in view of this involvement, it is suspected that the patient may have an associated vasculitis. After performing the biopsy and with the subsequent diagnosis of monoclonal gammopathy of uncertain significance, the diagnosis is made. We review the most recent bibliography of patients who have been diagnosed with crystalglobulinemia associated with plasma dyscrasia focusing in those with thrombotic vasculopathy or acute renal failure. In our case, in addition to being associated with monoclonal gammopathy of undetermined significance that is less frequent, the debut of the symptoms is years before the detection of the monoclonal peak. This could speak of patients with a low peak of monoclonal component (not detected by immunoelectrophoresis) who could have kidney and vascular damage.
Literature
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Metadata
Title
Crystalglobulinemia manifested as acute renal failure and thrombotic vasculopathy
Authors
L. Gómez-Lechón Quirós
M. E. Acosta De La Vega
O. Compán Fernández
S. Pastor Navarro
C. Montilla Morales
D. Moyano Bueno
J. Martín Centellas
A. Santos-Briz Terrón
C. Hidalgo Calleja
Publication date
01-08-2020
Publisher
Springer Berlin Heidelberg
Published in
Rheumatology International / Issue 8/2020
Print ISSN: 0172-8172
Electronic ISSN: 1437-160X
DOI
https://doi.org/10.1007/s00296-020-04620-6

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