Revista Médica de la Universidad de Costa Rica ISSN electrónico: 1659-2441

OAI: https://revistas.ucr.ac.cr/index.php/medica/oai
Wakdenström macroglobulinemia: case report and update
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Keywords

macroglobulinemia de waldenström
linfoma Linfoplasmocítico
síndrome de hiperviscosidad
waldenström macroglobulinemia
lymphoplasmacytic lymphoma
hyperviscosity syndrome

How to Cite

Quirós Quirós, W., & Rojas Castrillo, Y. (2013). Wakdenström macroglobulinemia: case report and update. Revista Médica De La Universidad De Costa Rica, 6(2), 64–71. https://doi.org/10.15517/rmu.v6i2.8071

Abstract

The Waldenström Macroglobulinemia is a rare hematologic malignancy characterized by medullar infiltration of  lymphocytes clonally related, which secrete monoclonal IgM protein. According to the World Health Organization  classification, this entity corresponds to a B-cell No Hodgkin Linfom known as lymphoplasmacytic lymphoma that occurs most often in people over 65 years and particularly in Caucasian males. It is essential to make a proper differential diagnosis between this disease and other similar entities associated with monoclonal component. The etiology is unknown but has been associated with genetic factors and family. We report a case of a patient with symptomatic Waldenström Macroglobulinemia, which present an aggressive clinical picture of retinal  bleeding  plus others typical signs caused by the disease.
https://doi.org/10.15517/rmu.v6i2.8071
PDF (Español (España))

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