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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...

詳細記述

保存先:
書誌詳細
出版年:Oxf Med Case Reports
主要な著者: Ayan, Mohamed S., Abdelrahman, Abd Almonem M., Khanal, Nabin, Elsallabi, Osama S., Birch, Nathan C.
フォーマット: Artigo
言語:Inglês
出版事項: Oxford University Press 2015
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4664885/
https://ncbi.nlm.nih.gov/pubmed/26634137
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omv025
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