Volume 50, Issue 1 pp. 49-52
Original Article
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Simultaneous occurrence of tetrasomy 21 and trisomy 8 in a patient with early blastic metamorphosis of chronic myeloproliferative disorder

Lucia Sebastio

Lucia Sebastio

Servizio Di Genetica Medica, Divisione di Ematologia, Napoli, Italia

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Dr. Felicetto Ferrara

Corresponding Author

Dr. Felicetto Ferrara

Servizio Di Genetica Medica, Divisione di Ematologia, Napoli, Italia

Via Pigna 76 F/G, 80128, Napoli, ItalySearch for more papers by this author
Laura Vicari

Laura Vicari

Servizio Di Genetica Medica, Divisione di Ematologia, Napoli, Italia

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Rosella Di Noto

Rosella Di Noto

Oncologia Sperimentale C, Istituto Nazionale dei Tumori, Napoli, Italia

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Luigi Del Vecchio

Luigi Del Vecchio

Servizio di Immunoematologia, Ospedale Cardarelli, Napoli, Italia

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Fabrizio Pane

Fabrizio Pane

Dipartimento di Biochimica e Ceinge, Universita Federico II, Napoli, Italia

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Alfredo Fasanaro

Alfredo Fasanaro

Dipartimento di Biochimica e Ceinge, Universita Federico II, Napoli, Italia

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Renato Cimino

Renato Cimino

Dipartimento di Biochimica e Ceinge, Universita Federico II, Napoli, Italia

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Francesco Salvatore

Francesco Salvatore

Dipartimento di Biochimica e Ceinge, Universita Federico II, Napoli, Italia

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Valerio Ventruto

Valerio Ventruto

Servizio Di Genetica Medica, Divisione di Ematologia, Napoli, Italia

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First published: September 1995
Citations: 7

Abstract

We report an unusual hyperdiploid karyotype characterized by the simultaneous occurrence of tetrasomy 21 and trisomy 8 detected during early blastic evolution of a BCR-ABL-negative chronic myeloproliferative disorder. Blast cells from this patient showed a striking response to all-trans-retinoic acid (ATRA)-induced differentiation as evaluated by CD15 expression following in vitro exposure to this inducer. Our report represents the first description of such a composite karyotype in human hematologic malignancies.

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