Wakdenström macroglobulinemia: case report and update
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| Autores: | , |
|---|---|
| 格式: | artículo original |
| 狀態: | Versión publicada |
| Fecha de Publicación: | 2013 |
| 實物特徵: | 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. |
| País: | Portal de Revistas UCR |
| 機構: | Universidad de Costa Rica |
| Repositorio: | Portal de Revistas UCR |
| 語言: | Español |
| OAI Identifier: | oai:portal.ucr.ac.cr:article/8071 |
| 在線閱讀: | https://revistas.ucr.ac.cr/index.php/medica/article/view/8071 |
| Palabra clave: | macroglobulinemia de waldenström linfoma Linfoplasmocítico síndrome de hiperviscosidad waldenström macroglobulinemia lymphoplasmacytic lymphoma hyperviscosity syndrome |