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星形细胞瘤的成骨细胞性转移:两例报告。

Osteoblastic metastases from astrocytomas: a report of two cases.

作者信息

Longee D C, Friedman H S, Phillips P C, Burger P C, Oakes W J, Heffez D, Wharam M, Strauss L, Fuller G N, Schold S C

机构信息

Department of Pediatrics, Duke University Medical Center, Durham, North Carolina.

出版信息

Med Pediatr Oncol. 1991;19(4):318-24. doi: 10.1002/mpo.2950190419.

Abstract

The spread of primary central nervous system (CNS) neoplasms beyond the confines of the neuraxis is a relatively uncommon observation. Extraneural metastases involving bone are quite rare, and have been observed almost exclusively in cases of medulloblastoma, high-grade (III-IV) astrocytoma, and glioblastoma multiforme. To date there has been only one case reported of bone metastasis from a "well-differentiated" astrocytoma. We now report two cases of astrocytoma in children with diffuse osteoblastic metastases and a fulminant clinical course. These cases demonstrate that due to the potential morphologic heterogeneity of these neoplasms, an initial biopsy diagnosis of low-grade astrocytoma does not always imply a benign clinical course.

摘要

原发性中枢神经系统(CNS)肿瘤扩散至神经轴范围之外是一种相对不常见的现象。涉及骨骼的神经外转移相当罕见,几乎仅在髓母细胞瘤、高级别(III - IV级)星形细胞瘤和多形性胶质母细胞瘤病例中观察到。迄今为止,仅有一例“高分化”星形细胞瘤发生骨转移的报告。我们现在报告两例儿童星形细胞瘤伴有弥漫性成骨转移及暴发性临床病程的病例。这些病例表明,由于这些肿瘤潜在的形态学异质性,最初活检诊断为低级别星形细胞瘤并不总是意味着临床病程良性。

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