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一名患有多形性胶质母细胞瘤的儿童在初诊时出现弥漫性骨转移。病例报告。

Diffuse bony metastases at presentation in a child with glioblastoma multiforme. A case report.

作者信息

Gamis A S, Egelhoff J, Roloson G, Young J, Woods G M, Newman R, Freeman A I

机构信息

Department of Pediatrics, Children's Mercy Hospital, University of Missouri-Kansas City School of Medicine, MO 64108.

出版信息

Cancer. 1990 Jul 1;66(1):180-4. doi: 10.1002/1097-0142(19900701)66:1<180::aid-cncr2820660132>3.0.co;2-m.

Abstract

At initial diagnosis, an 11-year-old girl with glioblastoma multiforme (GBM) presented with diffuse osteoblastic metastases. Primary brain tumors rarely metastasize outside of the central nervous system (CNS) without prior neurosurgery. Extracranial spread at diagnosis has been previously documented in just two adults. Extracranial metastasis of a childhood glioma without prior neurosurgery at any time during the course of the disease is exceedingly rare. Spread to bone by gliomas is also infrequent, and when they occur, bony metastases are usually isolated to one or two sites in any given patient. The widespread osseous metastases in our patient have been reported in three prior cases of high-grade gliomas. This child's GBM likely reflects a highly aggressive variant with the potential to spread outside the CNS and with a predilection for bone. Oncologists should be aware that GBM may present in this fashion during childhood.

摘要

初诊时,一名11岁的多形性胶质母细胞瘤(GBM)女孩出现弥漫性成骨性转移。原发性脑肿瘤在未经神经外科手术前很少转移至中枢神经系统(CNS)以外。诊断时颅外转移此前仅在两名成人患者中有记录。儿童胶质瘤在疾病过程中任何时候未经神经外科手术而发生颅外转移极为罕见。胶质瘤转移至骨骼也不常见,一旦发生,骨转移在任何给定患者中通常局限于一两个部位。我们患者广泛的骨转移在之前三例高级别胶质瘤病例中曾有报道。这名儿童的GBM可能反映了一种极具侵袭性的变体,有可能扩散至CNS以外并倾向于转移至骨骼。肿瘤学家应意识到GBM在儿童期可能以这种方式出现。

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