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  1. Chee CP
    Neurosurgery, 1987 Nov;21(5):749-51.
    PMID: 3696416
    The author describes a posterolateral extradural approach for total excision of small to moderate symptomatic lateral thoracic meningoceles. Its advantages over the classical laminectomy, intradural repair, and thoracotomy excision are discussed.
    Matched MeSH terms: Meningocele/surgery*
  2. Al-Edrus SA, Mohamed Mukari SA, Ganesan D, Ramli N
    Spine J, 2011 Aug;11(8):796-7.
    PMID: 21724472 DOI: 10.1016/j.spinee.2011.05.013
    Matched MeSH terms: Meningocele/surgery
  3. Donnenfeld AE, Hughes H, Weiner S
    Am J Perinatol, 1988 Jan;5(1):51-3.
    PMID: 3337758
    Frontoethmoidal meningoencephaloceles (FEM) are exceedingly rare in the western hemisphere, Australia, and Europe with an estimated frequency of 1 in 40,000 live births. Among the inhabitants of Thailand, Burma, Malaysia, Indonesia, and parts of the Soviet Union, however, the frequency is as high as 1 in 5000, accounting for 15% of all neural tube defects (NTD). Normal maternal serum alpha-fetoprotein (MSAFP) values usually will be found in these cases since most encephaloceles are closed, skin covered defects. Correct interpretation of the sonographic findings is crucial in establishing a diagnosis as well as giving prognostic and recurrence risk information. To our knowledge, this is the first reported case of prenatally diagnosed FEM. Perinatal management, differential diagnosis for disorders associated with this malformation, and epidemiologic information regarding this rare condition are discussed. It is anticipated that the prenatal sonographic findings may be applied to establish this diagnosis in similarly affected fetuses.
    Matched MeSH terms: Meningocele/surgery
  4. Sabir BI, Rahmat K, Bux SI, Rajagopal NS, Looi LM, Sia SF
    Clin Neurol Neurosurg, 2013 Oct;115(10):2192-6.
    PMID: 23791432 DOI: 10.1016/j.clineuro.2013.05.023
    Matched MeSH terms: Meningocele/surgery
  5. Thambidorai CR, Muin I, Razman J, Zulfiqar A
    Dis Colon Rectum, 2003 Jul;46(7):974-7.
    PMID: 12847376
    PURPOSE: Currarino triad, which comprises anorectal stenosis, anterior sacral defect, and a presacral mass, is an uncommon cause of constipation in children and adults. The presacral mass in this triad is most often caused by an anterior sacral meningocele, a teratoma, or an enterogenous cyst, but rarely may be caused by dual pathology. A neonate with Currarino triad and dual pathology in the presacral mass is described in this report.

    METHOD: A male Chinese neonate, who presented with abdominal distention and constipation on the second day of life, was found to have features of Currarino triad. Colostomy was done in the neonatal period, and the presacral mass was excised by posterior sagittal perineal approach at the age of six months.

    RESULTS: The excised presacral mass consisted of an anterior meningocele and a teratoma. The patient continued to have constipation during follow-up and required anorectoplasty to correct residual anorectal stenosis. At the time of this report the patient was three years old and growing normally with normal anorectal function.

    DISCUSSION: Of a total of about 200 cases of complete Currarino triad found in the literature, in only 22 patients did the presacral mass contain both meningocele and teratoma. The features of these 22 patients and the current views on the surgical management of Currarino triad are discussed.

    Matched MeSH terms: Meningocele/surgery
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