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2017, Número 2

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Rev Hematol Mex 2017; 18 (2)


Manifestación inusual de mieloma múltiple activo. Disfibrinogenemia adquirida e inhibidor del factor V

Suárez-González L, Sanabria-Alba L, García D, Paoletti M, Pepe A

Idioma: Español
Referencias bibliográficas: 22
Paginas: 92-98
Archivo PDF: 265.93 Kb.


RESUMEN

El mieloma múltiple es la segunda hemopatía maligna más frecuente (10%), seguida de los linfomas no Hodgkin. El cuadro clínico de manifestación suele estar en relación con los signos CRAB (hipercalcemia, insuficiencia renal, anemia y lesiones óseas) y en raras ocasiones puede manifestarse con sangrado por coagulopatías asociadas, como es el caso de la disfibrinogenemia e inhibidor del factor V de la coagulación. Este artículo describe un caso que fue derivado a nuestra consulta para estudio de anemia secundaria a sangrado y se revisa la bibliografía.


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