Pseudo-Pelger-Huët Anomaly in Megaloblastic Anemia

Journal Title: International Blood Research & Reviews - Year 2017, Vol 7, Issue 3

Abstract

The Pelger-Huët anomaly (PHA) is a morphologic abnormality of segmentation involving the neutrophils predominantly; however, all leucocytes may be variably affected; it is an autosomal dominant condition. It has a global prevalence; with certain Indian populations having a reported prevalence as high as 1 in 300. PHA should be considered when clinical labs suggest a profound left shift in the setting of normal leucocyte count. Clinically, PHA needs differentiation from the pseudo-Pelger-Huët anomaly (PPHA), which though morphologically similar is associated with multiple disease states such as; myelodysplasia, myeloproliferative disorders, leukemias, or drugs. PPHA with megaloblastic anemia is rarely seen. Reported herein, is a case of megaloblastic anemia with PPHA.

Authors and Affiliations

Ajay Kumar Khandal

Keywords

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  • EP ID EP306717
  • DOI 10.9734/IBRR/2017/34868
  • Views 139
  • Downloads 0

How To Cite

Ajay Kumar Khandal (2017). Pseudo-Pelger-Huët Anomaly in Megaloblastic Anemia. International Blood Research & Reviews, 7(3), 1-5. https://europub.co.uk/articles/-A-306717