Cutting L E, Koth C W, Burnette C P, Abrams M T, Kaufmann W E, Denckla M B
Developmental Cognitive Neurology, Kennedy Krieger Institute, Baltimore, MD 21205, USA.
J Child Neurol. 2000 Mar;15(3):157-60. doi: 10.1177/088307380001500303.
Using quantitative magnetic resonance imaging morphometry, we report that the whole brain volumes of patients with neurofibromatosis-1 are significantly larger than normal, confirm the prevalence of macrocephaly as about 50%, and report that macrocephaly in patients with neurofibromatosis-1 does not appear to be related to the familial or sporadic origin of the neurofibromatosis-1 or to the presence or absence of T2-weighted hyperintensities. No strong relationship emerged between the extent of neurofibromatosis-1-associated impairment of cognitive functions and degree of macrocephaly; however, the macrocephalic neurofibromatosis-1 group did have a significant verbal impairment relative to the nonmacrocephalic neurofibromatosis-1 group in vocabulary (P < .009).
通过定量磁共振成像形态学,我们报告1型神经纤维瘤病患者的全脑体积显著大于正常水平,证实巨头畸形的患病率约为50%,并报告1型神经纤维瘤病患者的巨头畸形似乎与1型神经纤维瘤病的家族性或散发性起源无关,也与T2加权高信号的有无无关。1型神经纤维瘤病相关的认知功能损害程度与巨头畸形程度之间未发现强相关性;然而,与非巨头畸形的1型神经纤维瘤病组相比,巨头畸形的1型神经纤维瘤病组在词汇量方面确实存在显著的语言损害(P < 0.009)。