Literature DB >> 343585

Chromosomal aneuploidy in a patient with hypereosinophilic syndrome. Evidence for a malignant disease.

J D Bitran, J D Rowley, F Plapp, H M Golomb, J E Ultmann.   

Abstract

A patient with rapidly fatal hypereosinophilic syndrome and a bone marrow chromosomal abnormality, 49,XYY,t(3:5),+8,+mar, is described. Scanning and transmission electron microscopy of eosinophils failed to reveal any significant abnormalities. Previous cytogenetic data on patients with hypereosinophilic syndrome have been deficient in that few studies have been performed with banding technics. These technics may help in the classification of hypereosinophilic syndrome and predict which patients will have a rapidly fatal course.

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Year:  1977        PMID: 343585     DOI: 10.1016/0002-9343(77)90556-3

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  3 in total

1.  Chromosomal mosaicism for inversion of chromosome 3(p25, p26) in a case of idiopathic hypereosinophilic syndrome (IHES).

Authors:  Nasim Valizadeh
Journal:  Indian J Hematol Blood Transfus       Date:  2011-12-13       Impact factor: 0.900

2.  Acute myelomonocytic leukaemia with abnormal eosinophils and inversion of chromosome 16.

Authors:  S Woessner; R Lafuente; L Florensa; J Sans-Sabrafen; J Antich
Journal:  Blut       Date:  1985-01

3.  Separation of hypereosinophilic syndrome from acute lymphoblastic leukemia with reactive eosinophilia.

Authors:  H S Markwell; E Wilson
Journal:  West J Med       Date:  1983-02
  3 in total

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