Invernizzi R, Custodi P, de Fazio P, Bergamaschi G, Fenoglio C, Ricevuti G, Rosti V, Zambelli L M, Ascari E
Dipartimenti di Medicina Interna (Sez. Clinica Medica II) e di Bioloiga Animale, Università, IRCCS Policlinico San Matteo, Pavia, Italy.
Haematologica. 1990 Nov-Dec;75(6):532-6.
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.
作者报告了一例罕见血液系统恶性肿瘤的临床和生物学发现,其形态学特征为粒细胞出现奇异的核异常,表现为染色质过度凝集以及明显的核碎裂,并伴有核分叶缺失。他们强调增殖和发育异常特征并存是该疾病的一个独特标志,并提出它可能代表非典型慢性髓系白血病(Ph1和ber阴性)中一种独特的罕见形态学实体。