Cohen Marta C, Karaman Ilgin, Squier Waney, Farrel Tom, Whitby Elspeth H
Department of Histopathology, Sheffield Children's NHS Foundation Trust, Sheffield, S10 2TH, UK.
Pediatr Dev Pathol. 2012 Jan-Feb;15(1):45-9. doi: 10.2350/10-01-0783-CR.1. Epub 2011 Jul 15.
Dandy-Walker malformation (DWM) is a developmental abnormality characterized by cystic dilatation of the fourth ventricle, complete or partial agenesis of the cerebellar vermis, and enlarged posterior fossa with upward displacement of the lateral sinuses, tentorium, and torcula. Calcification of brain tissue is a feature of congenital infection, particularly those involving the TORCH ( Toxoplasma gondii , rubella virus, Cytomegalovirus, and herpesvirus) group. An autosomal-recessive congenital infection-like syndrome with intracranial and extracranial calcifications has been categorized as pseudo-TORCH syndrome. We describe two male siblings diagnosed as DWM by ultrasound and by in utero and postmortem magnetic resonance imaging (MRI) but in whom the neuropathology revealed features of intracranial necrosis and calcification in the absence of extracranial calcific deposition. The fetal anomaly was identified by routine prenatal ultrasound scan at 16 weeks. In both cases the postmortem MRI showed bilateral ventriculomegaly with distortion of the overlying cortices, enlarged posterior fossa with a cyst related to small cerebellar hemispheres, and an incomplete cerebellar vermis. The diagnosis of DWM was offered. The histology revealed hypoplastic cerebral hemispheres with poorly cellular developing cortex. The white matter and periventricular matrix were disrupted by areas of necrosis and calcification not associated with any inflammatory infiltration, organisms, inclusions, or giant cells. To our knowledge, these two male siblings are the 1st cases that show pseudo-TORCH syndrome with distinctive intracranial calcification presenting as DWM. An autosomal-recessive or X-linked inheritance needs to be considered. Our study confirms the relevance of the multidisciplinary teamwork involved in the diagnosis of these complex cases.
丹迪-沃克畸形(DWM)是一种发育异常,其特征为第四脑室囊性扩张、小脑蚓部完全或部分发育不全,以及后颅窝增大伴外侧窦、小脑幕和窦汇向上移位。脑组织钙化是先天性感染的一个特征,尤其是那些涉及TORCH(弓形虫、风疹病毒、巨细胞病毒和疱疹病毒)组的感染。一种伴有颅内和颅外钙化的常染色体隐性先天性感染样综合征已被归类为假性TORCH综合征。我们描述了两名男性同胞,他们通过超声以及产前和产后磁共振成像(MRI)被诊断为DWM,但神经病理学显示其颅内有坏死和钙化特征,而颅外无钙化沉积。胎儿异常在孕16周时通过常规产前超声扫描发现。在这两个病例中,死后MRI均显示双侧脑室扩大,上方皮质变形,后颅窝增大,伴有与小脑半球小有关的囊肿,以及小脑蚓部不完整。诊断为DWM。组织学显示大脑半球发育不全,皮质细胞发育不良。白质和脑室周围基质被坏死和钙化区域破坏,这些区域与任何炎症浸润、生物体、包涵体或巨细胞无关。据我们所知,这两名男性同胞是首例表现为假性TORCH综合征且伴有独特颅内钙化并呈现DWM的病例。需要考虑常染色体隐性或X连锁遗传。我们的研究证实了多学科团队合作在诊断这些复杂病例中的相关性。