| Literature DB >> 26778239 |
Jan Palmblad1, Christer C Nilsson1, Petter Höglund2, Helen A Papadaki3.
Abstract
Neutropenias (NPs), being acute and often transient, or chronic, range from life-threatening conditions with very low absolute neutrophil blood counts (ANC) to disorders characterized by only mild NP and of no obvious significance for health. Many are caused by genetic variations/mutations, e.g. the benign familial NP and the chronic severe NPs (e.g. Kostmann disease). Some of the latter are associated with various bodily malformations. Many of the mild-to-moderate NPs are signs of underlying disorders that need specialized treatments (e.g. HIV, hepatitis, autoimmune disorders, the large granular lymphocyte syndrome). We provide here means for the evaluation of a previously unknown NP, suggest a triage and treatments.Entities:
Keywords: G-CSF; Neutropenia; adverse drug reactions; agranulocytosis; autoimmune neutropenia; idiopathic neutropenia; large granular lymphocytosis; plerixafor; severe chronic neutropenia
Mesh:
Year: 2016 PMID: 26778239 DOI: 10.1586/17474086.2016.1142867
Source DB: PubMed Journal: Expert Rev Hematol ISSN: 1747-4094 Impact factor: 2.929