Leech R W, Johnson S H, Brumback R A
Department of Pathology, University of Oklahoma College of Medicine, Oklahoma City 73190, USA.
Clin Neuropathol. 1997 Mar-Apr;16(2):90-7.
Complete cerebellar agenesis or aplasia is an extremely rare condition with few previously reported cases. We identified a 38-week gestation infant with microcephaly who had complete cerebellar agenesis associated with arrhinecephaly. There was complete lack of the efferent and afferent limbs of the cerebellum, including the nuclei of the basis pontis, the inferior olivary nuclei, ascending spinal and medullary afferents, deep cerebellar nuclei and their afferents, and the red nucleus. Although complete cerebellar agenesis is rare, cerebellar hypoplasia is more common and can be sporadic, asymmetric, or represent clinically, genetically, and pathologically diverse examples of primary cerebellar or vermian hypoplasia.
完全性小脑发育不全或发育不良是一种极其罕见的病症,此前报道的病例很少。我们鉴定出一名孕38周的小头畸形婴儿,其患有与无脑畸形相关的完全性小脑发育不全。小脑的传出和传入肢体完全缺失,包括脑桥基底部核、下橄榄核、脊髓和延髓上行传入纤维、小脑深部核及其传入纤维以及红核。虽然完全性小脑发育不全很罕见,但小脑发育不全更为常见,可为散发性、不对称性,或代表原发性小脑或蚓部发育不全在临床、遗传和病理方面的多种不同实例。