SMD - Portaobjetos 1
Diapositiva de un paciente diagnosticado de síndrome mielodisplásico con exceso de blastos, tipo 2. El SMD-EB2 se define como la aparición de mielodisplasia en combinación con un 5-19% de blastos en sangre periférica. En este paciente, los granulocitos neutrófilos muestran propiedades displásicas con granulación reducida y una forma nuclear anormal (pseudo-pelger huet).
Blastos
Promielocitos
Mielocitos
Metamielocitos
Bandas
Segmentados
Basófilos
Linfocitos
Eritroblastos
Médula ósea
![](https://cdn.cellwiki.net/db/pathology/page-188/gallery-794/001-preview.webp)
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Blastos
![](https://cdn.cellwiki.net/db/pathology/page-188/gallery-1350/001.jpg)
![](https://cdn.cellwiki.net/db/pathology/page-188/gallery-1350/002.jpg)
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![](https://cdn.cellwiki.net/db/pathology/page-188/gallery-1350/007.jpg)
![](https://cdn.cellwiki.net/db/pathology/page-188/gallery-1350/008.jpg)
Pseudo Pelger-Huët
![](https://cdn.cellwiki.net/db/pathology/page-188/gallery-795/001.jpg)
![](https://cdn.cellwiki.net/db/pathology/page-188/gallery-795/002.jpg)
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