Humphreys Peter, Muzumdar Dattatraya P, Sly Lloyd E, Michaud Jean
Department of Pediatrics (Neurology Division), Children's Hospital of Eastern Ontario, and University of Ottawa, Ottawa, Ontario, Canada.
Pediatr Neurol. 2007 Apr;36(4):236-43. doi: 10.1016/j.pediatrneurol.2006.12.013.
A variety of developmental brain anomalies have been described in individuals with fetal hydrocephalus, regardless of etiology. Examples include callosal dysgenesis, periventricular gray matter heterotopia, hippocampal and white matter hypoplasia, and cortical polygyration. The present report draws attention to another anomaly not reported in previous case series of fetal hydrocephalus: focal cerebral mantle disruption. Neonatal imaging findings (where available) and post-shunt, stable-state magnetic resonance imaging, or pathological findings were reviewed in 77 subjects with fetal hydrocephalus (55 myelomeningocele, 16 sporadic aqueductal stenosis, 6 miscellaneous). Of these, 12 subjects (15.6%) demonstrated a combination of absence of the septum pellucidum and severe thinning or absence of the posteromesial cerebral mantle. On axial sequences, this combination created the illusion of a common ventricle, as in lobar holoprosencephaly. All 12 subjects had massive hydrocephalus at birth, accompanied in 7 by posteromesial ventricular diverticula. Two subjects, and one other subject with distinct lateral ventricles, demonstrated unilateral or bilateral mantle clefts suggestive of schizencephaly. Close radiological (n = 2) or pathological (n = 1) inspection showed that the clefts were only partially lined with gray matter and contained a transverse gliotic membrane. These findings are consistent with the hypothesis that massive early fetal hydrocephalus may completely disrupt cerebral mantle formation, particularly in the posteromesial hemispheres.
无论病因如何,胎儿脑积水患者已被描述出多种脑发育异常情况。例如胼胝体发育不全、脑室周围灰质异位、海马和白质发育不全以及皮质多回畸形。本报告提请注意胎儿脑积水既往病例系列中未报道的另一种异常:局灶性脑皮质破坏。对77例胎儿脑积水患者(55例脊柱裂脊膜膨出、16例散发性导水管狭窄、6例其他)的新生儿影像学检查结果(若有)以及分流术后稳态磁共振成像或病理检查结果进行了回顾。其中,12例患者(15.6%)表现为透明隔缺如以及大脑后内侧皮质严重变薄或缺失。在轴位序列上,这种情况造成了类似叶状全前脑畸形中共同脑室的假象。所有12例患者出生时均有大量脑积水,其中7例伴有后内侧脑室憩室。2例患者以及另1例有明显侧脑室的患者表现出提示脑裂畸形的单侧或双侧皮质裂。细致的影像学检查(2例)或病理检查(1例)显示,这些裂隙仅部分衬有灰质,并含有横向胶质膜。这些发现与以下假设一致,即早期严重胎儿脑积水可能完全破坏脑皮质形成,尤其是在后内侧半球。