Abstract |
We report a case of an unusual myeloproliferative disorder with trisomy of chromosome 8 characterized by peripheral blood thrombocythaemia and pronounced bone marrow myelodysplastic features. Treatment with interferon-alpha at intermediate dosages, together with a complete bone marrow and peripheral blood haematology remission, was able to induce a cytogenetic remission, shown by the complete disappearance at the conventional cytogenetic analysis of trisomy 8 abnormality characterizing the neoplastic clone at diagnosis. However, trisomy 8 was still detectable by FISH in a small proportion of cells, showing that profound suppression of, but not complete eradication of, the neoplastic clone had occurred. The ability of interferon-alpha to induce a major cytogenetic remission in a +8, Philadelphia-chromosome negative, myeloproliferative disorder has not previously been documented and may provide further indications for the use of this drug in these disorders.
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Authors | M Petrini, P Simi, G Saglio |
Journal | British journal of haematology
(Br J Haematol)
Vol. 92
Issue 4
Pg. 941-3
(Mar 1996)
ISSN: 0007-1048 [Print] England |
PMID | 8616089
(Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Adult
- Chromosomes, Human, Pair 8
- Humans
- In Situ Hybridization, Fluorescence
- Interferon-alpha
(therapeutic use)
- Male
- Myeloproliferative Disorders
(genetics, therapy)
- Trisomy
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