Wakdenström macroglobulinemia: case report and update
保存先:
| 著者: | , |
|---|---|
| フォーマット: | artículo original |
| 状態: | Versión publicada |
| 出版日付: | 2013 |
| その他の書誌記述: | 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. |
| 国: | Portal de Revistas UCR |
| 機関: | Universidad de Costa Rica |
| Repositorio: | Portal de Revistas UCR |
| 言語: | Español |
| OAI Identifier: | oai:portal.ucr.ac.cr:article/8071 |
| オンライン･アクセス: | https://revistas.ucr.ac.cr/index.php/medica/article/view/8071 |
| キーワード: | macroglobulinemia de waldenström linfoma Linfoplasmocítico síndrome de hiperviscosidad waldenström macroglobulinemia lymphoplasmacytic lymphoma hyperviscosity syndrome |