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复合型神经节神经母细胞瘤。对婴儿期后诊断的神经母细胞瘤中组织学成熟度意义的评估。

Composite ganglioneuroblastoma. An assessment of the significance of histological maturation in neuroblastoma diagnosed beyond infancy.

作者信息

Bove K E, McAdams A J

出版信息

Arch Pathol Lab Med. 1981 Jun;105(6):325-30.

PMID:6894529
Abstract

At Cincinnati Childrens Hospital Medical Center, 19 cases of composite ganglioneuroblastoma (CGNB) comprise one third of the cases of neuroblastoma diagnosed after 1 year of age. We have not identified this condition in an infant. Usually located in the mediastinum, CGNB is typically resectable and has a favorable prognosis, but retains potential to metastasize until nests of neuroblasts have disappeared. Prognosis is independent of proportion of ganglioneuroma or neuroblastoma and is closely related to stage. The interval between diagnosis and death in fatal CGNB was typically prolonged. Survival of older children with poorly differentiated neuroblastoma was rare and neuromatous maturation was absent or trivial in unresected primary tumors studied at the time of autopsy. We conclude that favorable outcome in neuroblastoma diagnosed after 1 year of age is closely related to histological maturation as herein defined.

摘要

在辛辛那提儿童医院医疗中心,19例复合性神经节神经母细胞瘤(CGNB)占1岁以后诊断出的神经母细胞瘤病例的三分之一。我们在婴儿中未发现这种情况。CGNB通常位于纵隔,通常可切除且预后良好,但在神经母细胞巢消失之前仍有转移的可能。预后与神经节瘤或神经母细胞瘤的比例无关,而与分期密切相关。致命性CGNB从诊断到死亡的间隔通常较长。年龄较大的低分化神经母细胞瘤患儿的存活率很低,在尸检时研究的未切除原发性肿瘤中,神经瘤成熟不存在或很轻微。我们得出结论,1岁以后诊断出的神经母细胞瘤的良好预后与本文所定义的组织学成熟密切相关。

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