Lena G, van Calenberg F, Genitori L, Choux M
Department of Pediatric Neurosurgery, Hôpital des Enfants, La Timone, Marseille, France.
Childs Nerv Syst. 1995 Oct;11(10):568-73. doi: 10.1007/BF00300994.
Cerebrospinal-fluid-filled interhemispheric cysts associated with callosal agenesis are relatively rare lesions, and have been subject to a varied and confusing terminology. From a pragmatic surgical point of view, we believe that the dorsal III ventricular cyst [35] and the giant interhemispheric cyst [23], although of different embryological origin, can be classified as one group. The most important condition that must be distinguished from interhemispheric cysts is the alobar form of holoprosencephaly. We describe the clinical symptomatology in 16 children who were surgically treated with a cysto-peritoneal shunt. The outcome, both neurologically and developmentally, was good in the large majority of cases, and compared favorably to similar cases in the older literature. It therefore seems reasonable, at the present state of knowledge and until further studies clarify the origin and natural history of these cysts, to treat them as early as possible in order to prevent gross developmental deficits.
与胼胝体发育不全相关的充满脑脊液的半球间囊肿是相对罕见的病变,并且有各种各样令人困惑的术语。从务实的手术角度来看,我们认为背侧第三脑室囊肿[35]和巨大半球间囊肿[23],尽管胚胎学起源不同,但可归为一组。必须与半球间囊肿区分开的最重要情况是无脑叶型前脑无裂畸形。我们描述了16例接受囊肿 - 腹腔分流手术治疗的儿童的临床症状。在大多数病例中,神经和发育方面的结果良好,与旧文献中的类似病例相比具有优势。因此,在目前的知识水平下,并且在进一步研究阐明这些囊肿的起源和自然史之前,尽早治疗它们以防止严重的发育缺陷似乎是合理的。