SciELO - Scientific Electronic Library Online

 
vol.86 número2Diagnosis of proximal colonic cancer due to hemorrhagic complication of thrombolytic therapy on myocardial infarctionReport of a case of liver rupture in preeclampsia and HELLP syndrome índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

  • No hay artículos similaresSimilares en SciELO

Compartir


Revista médica del Hospital General de México

versión On-line ISSN 2524-177Xversión impresa ISSN 0185-1063

Resumen

NAVARRO-OLVERA, José L. et al. A rare association between intracranial neuroenteric cyst and Klippel-Feil syndrome: a case report. Rev. med. Hosp. Gen. Méx. [online]. 2023, vol.86, n.2, pp.79-84.  Epub 16-Oct-2023. ISSN 2524-177X.  https://doi.org/10.24875/hgmx.22000050.

Neuroenteric cysts (NEC) are congenital malformations of endodermal origin, denoting 0.01% of all tumors, where most of these lesions have a spinal location. The authors reported a case that presents an intracranial NEC and Klippel-Feil syndrome (KFS) simultaneously. A 21-year-old male patient with clinical data related with KFS presented to the hospital with obstructive hydrocephalus secondary to an infratentorial lesion, located in the right cerebellum. An urgent ventriculoperitoneal shunt was placed and a midline suboccipital craniectomy with resection of C1 posterior arch and tumor excision was carried out, obtaining a lesion characteristic of NEC through histopathological study.

Palabras llave : Neuroenteric cyst; Intracranial; Posterior fossa; Klippel-Feil syndrome; Neurosurgery.

        · texto en Inglés     · Inglés ( pdf )