Mieloma IgD: una infrecuente observación

Authors

  • René Hernández Benedicto
  • Rafael Pila Pérez
  • Rafael Pila Peláez
  • Víctor A. Holguín Prieto

Abstract

Se describe el caso de un paciente de 50 años, masculino, con el diagnóstico de un mieloma IgD, que debuta con la presencia de anemia y dolores óseos generalizados. Se destaca la baja frecuencia de este subtipo de mieloma y su comportamiento biológico. El mieloma IgD constituye solamente el 2, 1 % de todos los mielomas. El peor pronóstico del MM IgD con respecto a otro tipo de mielomas está en relación con la mayor frecuencia de insuficiencia renal, invasiones extraóseas y amiloidosis que se presentan. Se describen las características clínicas y humorales del paciente. Se resalta el estudio diagnóstico y la terapéutica empleada.

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Published

2014-11-11

How to Cite

1.
Hernández Benedicto R, Pila Pérez R, Pila Peláez R, Holguín Prieto VA. Mieloma IgD: una infrecuente observación. Arch méd Camagüey [Internet]. 2014 Nov. 11 [cited 2025 Oct. 20];11(3). Available from: https://revistaamc.sld.cu/index.php/amc/article/view/2704

Issue

Vol. 11 No. 3 (2007)

Section

Case Reports

License

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