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Cystic spinal dysraphism of the cervical and upper thoracic region.

Cystic spinal dysraphism of the cervical and upper thoracic region. Research Abstract Details 

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  • Cystic spinal dysraphism of the cervical and upper thoracic region. Abstract Text:

    j francisco J Francisco , cavalheiro Cavalheiro,hamilton matushitaHamilton Matushita, leibinger Leibinger,antonio r bellasAntonio R Bellas,elide vanazziElide Vanazzi,luiz a m de souzaLuiz A M de Souza, nardi Nardi,

    BACKGROUND: Cystic dysraphic lesions of the cervical and upper thoracic region are rare and only a few series have been published about the topic. These malformations can be divided into categories that include both myelocystoceles and the so-called cervical meningoceles or myelomeningoceles. METHODS: A retrospective study of 18 patients was conducted. RESULTS: In 17 patients a squamous or a cicatricial epithelium of variable thickness covered the dome of the lesions, while the base was covered with full-thickness skin. In one case the skin was entirely normal. Four patients displayed associated CNS malformations and three more had systemic congenital anomalies. All patients underwent surgical exploration and the length of time between birth and surgery ranged from 6 h to 9 months. The most frequent surgical finding, seen in 14 patients, was a stalk connecting the dorsal surface of the spinal cord to the cyst. In three patients the findings were consistent with myelocystocele. Only in one case was a true meningocele found. Hydrocephalus and Chiari II malformation were not as consistently associated as in myelomeningoceles. Neurological signs and symptoms were not so marked as in myelomeningoceles and were found in the follow-up of four patients. In two of them there was a non-progressive deficit, probably expressing an imperceptible involvement of the nervous system in the first year of life. The histopathological findings were of three types: neuroglial stalks, fibrovascular stalks and myelocystoceles. CONCLUSIONS: Cystic dysraphisms of the cervical and upper thoracic region differ clinically and structurally from meningomyelocele and have a more favorable outcome. We believe that these malformations have not been properly labeled and propose a classification based on the structures found inside the cyst.

    Cystic spinal dysraphism of the cervical and upper thoracic region. Publishing Authors By Initials

    jf JF ,s cavalheiroS Cavalheiro,h matushitaH Matushita,rd leibingerRD Leibinger,ar bellasAR Bellas,e vanazziE Vanazzi,la de souzaLA de Souza,ag nardiAG Nardi,

    For similar abstracts research abstracts see: abstracts research

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    Cystic spinal dysraphism of the cervical and upper thoracic region. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Child's nervous system : ChNS : official journal o

    VOLUME: 22

    Page Numbers: 234-42

    Journal Abbreviation:

    ISSN: 0256-7040

    DAY: 4

    MONTH: 06

    YEAR: 2005

    Cystic spinal dysraphism of the cervical and upper thoracic region. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8503227

    Cystic spinal dysraphism of the cervical and upper thoracic region. Keywords Mesh Terms:

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    Grant and Affiliation Information for Cystic spinal dysraphism of the cervical and upper thoracic region.

    AFFILIATION: Section of Pediatric Neurosurgery, Department of Pediatric Surgery, Fernandes Figueira Institute, Oswaldo Cruz Foundation MS-Fiocruz, Av. Rui Barbosa, 716, Rio de Janeiro, Brazil. fsalomao@ism.com.br

    Country: Germany

    Germany Research PublicationGermany Research Publication

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    MEDLINETA: Childs Nerv Syst

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