Literature DB >> 10996825

Dysplastic changes in idiopathic thrombocytopenic purpura and the effect of corticosteroids to increase dysplasia and cause hyperdiploid macropolycytes.

L Olcay1, S Yetgin, H Okur, S Erekul, M Tuncer.   

Abstract

This study evaluates the dysplastic hematological changes in nine patients with idiopathic thrombocytopenic purpura (ITP) in 11 attacks, before and after corticosteroid treatment. The pretreatment blood smears of patients with ITP, displayed more neutrophils with bizarre nuclei (P < 0.001), Döhle or Döhle-like inclusions (P < 0. 01), irregular distribution of granules (P < 0.05), hypo-agranulation (P < 0.05), pseudo-Pelger-Huet-like cells (P < 0. 01), and nuclei with chromatine clumping (P < 0.01) than the normal children. The eosinophils of ITP patients were also dysplastic, before treatment. The pretreatment diameter of the neutrophils and the percentage of macropolycytes were greater than those of the patients with viral infections and normal group (P < 0.05 for all). The percentage of neutrophils with bizarre nuclei and nuclei with chromatine clumping and the diameter of neutrophils and macropolycyte percentage increased with corticosteroid therapy (P < 0.01, < 0.01, < 0.01, and < 0.05, respectively). The neutrophil diameter, percentage of macropolycytes, and number of neutrophils with bizarre nuclei decreased within 1-4 weeks after the therapy was stopped. In the neutrophils of two patients, diploidy and hyperdiploidy were established before and on the last day of therapy, respectively, and diploidy reversed after therapy was stopped. In conclusion, ITP patients display dysplastic findings in both neutrophils and eosinophils before treatment and corticosteroids cause transient significant increase in some of the dysplastic changes in neutrophils. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10996825     DOI: 10.1002/1096-8652(200010)65:2<99::aid-ajh2>3.0.co;2-k

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  2 in total

1.  A child with psoriasis, hypogammaglobulinemia, and monosomy 7-positive myelodysplastic syndrome.

Authors:  Namık Özbek; Arzu Yazal Erdem; Özlem Arman Bilir; Fatma Karaca Kara; Mutlu Yüksek; Neşe Yaralı; Meltem Özgüner; Nazmiye Yüksek; Bahattin Tunç
Journal:  Turk J Haematol       Date:  2015-03-05       Impact factor: 1.831

2.  Both Granulocytic and Non-Granulocytic Blood Cells Are Affected in Patients with Severe Congenital Neutropenia and Their Non-Neutropenic Family Members: An Evaluation of Morphology, Function, and Cell Death

Authors:  Lale Olcay; Şule Ünal; Hüseyin Onay; Esra Erdemli; Ayşenur Öztürk; Deniz Billur; Ayşe Metin; Hamza Okur; Yıldız Yıldırmak; Yahya Büyükaşık; Aydan İkincioğulları; Mesude Falay; Gülsüm Özet; Sevgi Yetgin
Journal:  Turk J Haematol       Date:  2018-07-24       Impact factor: 1.831

  2 in total

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