Donaldson Sarah S, Laningham Fred, Fisher Paul Graham
Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA.
J Clin Oncol. 2006 Mar 10;24(8):1266-72. doi: 10.1200/JCO.2005.04.6599.
The diagnosis of brainstem glioma was long considered a single entity. However, since the advent of magnetic resonance imaging in the late 1980s, neoplasms within this anatomic region are now recognized to include several tumors of varying behavior and natural history. More recent reports of brainstem tumors include diverse sites such as the cervicomedullary junction, pons, midbrain, or the tectum. Today, these tumors are broadly categorized as either diffuse intrinsic gliomas, most often in the pons, or the nondiffuse brainstem tumors originating at the tectum, focally in the midbrain, dorsal and exophytic to the brainstem, or within the cervicomedullary junction. Although we briefly discuss the nondiffuse tumors, we focus specifically on those diffuse brainstem tumors that regrettably still carry a bleak prognosis.
脑干胶质瘤的诊断长期以来被视为单一疾病。然而,自20世纪80年代末磁共振成像出现以来,现在人们认识到这个解剖区域内的肿瘤包括几种行为和自然病程各异的肿瘤。最近关于脑干肿瘤的报告包括不同部位,如颈髓交界处、脑桥、中脑或顶盖。如今,这些肿瘤大致分为两类,一类是弥漫性固有胶质瘤,最常见于脑桥,另一类是非弥漫性脑干肿瘤,起源于顶盖、中脑局部、脑干背侧并向外生长或位于颈髓交界处。虽然我们简要讨论了非弥漫性肿瘤,但我们特别关注那些预后仍然令人悲观的弥漫性脑干肿瘤。