Case of acquired or pseudo-Pelger-Huët anomaly

Pelger-Huët anomaly (PHA) is a rare benign autosomal-dominant anomaly with an incidence of ∼1 in 6000. It does not cause neutrophilia, but it can cause a false increase in band forms. It should be differentiated from acquired or pseudo-Pelger-Huët anomaly (PPHA), which has similar morphology, howeve...

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Detalles Bibliográficos
Autores principales: Ayan, Mohamed S., Abdelrahman, Abd Almonem M., Khanal, Nabin, Elsallabi, Osama S., Birch, Nathan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664885/
https://www.ncbi.nlm.nih.gov/pubmed/26634137
http://dx.doi.org/10.1093/omcr/omv025

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664885/
https://www.ncbi.nlm.nih.gov/pubmed/26634137
http://dx.doi.org/10.1093/omcr/omv025

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