The authors report the clinical and biological findings of a case of a rare haematological malignant entity, morphologically characterised by a bizarre nuclear abnormality in granulocytes, consisting of exaggerated chromatin clumping and apparent fragmentation of the nucleus, with a loss of segmentation. They emphasize the coexistence of proliferative and dysplastic characteristics as a distinctive marker of this disorder and suggest it may represent a distinct rare morphological entity among the atypical chronic myeloid leukaemias, Ph1 and ber negative.

The syndrome of abnormal chromatin clumping in leucocytes: clinical and biological study of a case.

INVERNIZZI, ROSANGELA;FENOGLIO, CARLA;RICEVUTI, GIOVANNI;ASCARI, EDOARDO
1990-01-01

Abstract

The authors report the clinical and biological findings of a case of a rare haematological malignant entity, morphologically characterised by a bizarre nuclear abnormality in granulocytes, consisting of exaggerated chromatin clumping and apparent fragmentation of the nucleus, with a loss of segmentation. They emphasize the coexistence of proliferative and dysplastic characteristics as a distinctive marker of this disorder and suggest it may represent a distinct rare morphological entity among the atypical chronic myeloid leukaemias, Ph1 and ber negative.
1990
The Hematology category covers resources concerned with blood, blood-forming tissues, bone marrow, plasma, and transfusions. Coverage also includes resources on specialties such as hemophilia, leukemia, and lymphoma.
Sì, ma tipo non specificato
Inglese
Internazionale
STAMPA
75
6
532
536
5
Chromatin clumping; Myelodysplasia; Atypical chronic myeloid leukemia
9
info:eu-repo/semantics/article
262
Invernizzi, Rosangela; P., Custodi; P., De Fazio; G., Bergamaschi; Fenoglio, Carla; Ricevuti, Giovanni; V., Rosti; L. M., Zambelli; Ascari, Edoardo...espandi
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/439713
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