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Open AccessJournal ArticleDOI

Gammapatías monoclonales de significado renal

Fernando Caravaca-Fontán, +3 more
- 01 Sep 2017 - 
- Vol. 37, Iss: 5, pp 465-477
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TLDR
La importancia de discriminar el termino GMSR radica en poder indicar procedimientos diagnosticos y terapeuticos dirigidos al control of the sintesis y secrecion of las proteinas monoclonales independientemente of los criterios clasicos vinculados with the expansion tumoral maligna.
Abstract
The term monoclonal gammopathy of renal significance (MGRS) comprises a group of diseases pathogenetically characterised by proliferation of a B-cell or plasma cell clone that synthesises and secretes a monoclonal immunoglobulin or its components (light and/or heavy chains), that may deposit and cause glomerular, tubular, interstitial and/or vascular damage. The importance of differentiating the term MGRS from other monoclonal gammopathies lies in the fact that diagnostic and therapeutic procedures aimed at controlling monoclonal protein synthesis and secretion can be indicated, irrespective of the classic criteria based on malignant tumour expansion. Renal pathology associated with MGRS is highly heterogeneous, and therefore renal biopsy should be considered a key diagnostic tool. A precise diagnostic approach, however, must also identify the monoclonal protein in plasma and/or in urine, together with a complete haematological study in order to determine the nature and extension of cell clones. Recent advances in the understanding of these entities have resulted in significant improvements in clinical course and survival in several forms of MGRS, although more studies and clinical experience are needed in order to delineate more effective therapeutic strategies. In this review, we summarise the main clinical and pathological features of MGRS, highlighting the most appropriate diagnostic approach and current therapeutic options.

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Citations
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Update on C3 Glomerulopathy: A Complement-Mediated Disease.

TL;DR: In recent years, several important advances have taken place in the understanding of C3G, but still further studies are warranted to elucidate the best therapeutic strategies that could improve prognosis of this entity.
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Chronological change of renal pathological findings in the proliferative glomerulonephritis with monoclonal IgG deposits considered to have recurred early after kidney transplantation.

TL;DR: The case of a 46-year-old man who presented with nephrotic syndrome and progressive kidney injury following kidney transplantation and was diagnosed with recurrent PGNMID case in the allograft, where the graft function was eventually lost.
References
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Journal ArticleDOI

Criteria for the classification of monoclonal gammopathies, multiple myeloma and related disorders: a report of the International Myeloma Working Group

TL;DR: The International Myeloma Working Group has reviewed the criteria for diagnosis and classification with the aim of producing simple, easily used definitions based on routinely available investigations to facilitate comparison of therapeutic trial data.
Journal ArticleDOI

Prevalence of Monoclonal Gammopathy of Undetermined Significance

TL;DR: Among residents of Olmsted County, Minnesota, MGUS was found in 3.2% of persons 50 years of age or older and 5.3 percent of persons 70 years ofAge or older, which are higher in men than in women.
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