Preterm-related posthemorrhagic hydrocephalus: Review of our institutional series with a long-term follow-up / Hidrocefalia poshemorrágica del prematuro: revisión de nuestra serie a largo plazo

Introduction Preterm-related posthemorrhagic hydrocephalus is a major cause of neurological impairment and a common indication for a ventriculoperitoneal shunt in infants that are prone to diverse complications. Protocols of diagnosis and treatment are in continuous evolution and require evaluation of their results. Objective To review the clinical characteristics and results of a series of preterm-related posthemorrhagic hydrocephalus needing a definitive shunt from 1982 to 2020 in our institution. As a secondary objective we evaluated the safety of the changes in our protocol of treatment from 2015. Methods Retrospective review, clinical investigation. Results 133 patients were implanted a shunt in the study period. Shunt infection was diagnosed in 15 patients. Proximal shunt obstruction as the first complication was diagnosed in 30% of cases at one year, 37% at two years and 46% at five years. 61 patients developed very small or collapsed ventricles at last follow-up. Two thirds of our patients achieved normal neurological development or mild impairment. Changes in protocol did not significantly modify clinical results although improvement in most outcomes was observed. Mean follow-up was over nine years. Conclusions Clinical outcomes are comparable to previous reported data. Changes in protocol proved to be safe and improved our results. Programmable shunts can be used safely in preterm patients although they may not prevent tendency towards ventricular collapse, which is very common after long follow-up (AU)

Antecedentes La hidrocefalia poshemorrágica del prematuro continúa siendo una causa importante de lesión cerebral perinatal y una indicación frecuente de cirugía derivativa valvular en un grupo de pacientes particularmente vulnerable y expuesto a complicaciones. Los protocolos de diagnóstico y tratamiento están en continua evolución y requieren un análisis de los resultados asociados a ellos. Objetivo Revisar las características clínicas y los resultados de tratamiento en una serie de prematuros con hidrocefalia poshemorrágica en los que se implantó una derivación ventriculoperitoneal permanente en nuestro hospital entre 1982 y 2000. Como objetivo secundario evaluamos la seguridad de los cambios introducidos en nuestro protocolo desde 2015. Material y método Estudio clínico retrospectivo, serie de casos. Resultados 133 prematuros requirieron una derivación ventriculoperitoneal permanente en el tiempo de estudio. En 15 de ellos se diagnosticó una infección del sistema de derivación. La obstrucción proximal de la derivación como primera complicación posquirúrgica ocurrió en un 30% de los pacientes al primer año, en el 37% de los pacientes a los dos años y en el 46% de los casos a los 5 años de seguimiento. 61 pacientes desarrollaron un colapso ventricular clínico o radiológico. Dos tercios de los pacientes presentaron un desarrollo psicomotor normal o un retraso de carácter leve. Los cambios incorporados en nuestro protocolo de tratamiento no modificaron la evolución clínica significativamente, aunque se asociaron a una evolución globalmente más favorable. La media de seguimiento fue superior a los 9 años. Conclusiones Los resultados clínicos presentados se encuentran en línea con las series publicadas, Los cambios incorporados en nuestro protocolo actualizado demostraron ser seguros y pueden asociarse a una evolución más favorable (AU)

Preterm-related posthemorrhagic hydrocephalus: Review of our institutional series with a long-term follow-up.

INTRODUCTION: Preterm-related posthemorrhagic hydrocephalus is a major cause of neurological impairment and a common indication for a ventriculoperitoneal shunt in infants that are prone to diverse complications. Protocols of diagnosis and treatment are in continuous evolution and require evaluation of their results. OBJECTIVE: To review the clinical characteristics and results of a series of preterm-related posthemorrhagic hydrocephalus needing a definitive shunt from 1982 to 2020 in our institution. As a secondary objective we evaluated the safety of the changes in our protocol of treatment from 2015. METHODS: Retrospective review, clinical investigation. RESULTS: 133 patients were implanted a shunt in the study period. Shunt infection was diagnosed in 15 patients. Proximal shunt obstruction as the first complication was diagnosed in 30% of cases at one year, 37% at two years and 46% at five years. 61 patients developed very small or collapsed ventricles at last follow-up. Two thirds of our patients achieved normal neurological development or mild impairment. Changes in protocol did not significantly modify clinical results although improvement in most outcomes was observed. Mean follow-up was over nine years. CONCLUSIONS: Clinical outcomes are comparable to previous reported data. Changes in protocol proved to be safe and improved our results. Programmable shunts can be used safely in preterm patients although they may not prevent tendency towards ventricular collapse, which is very common after long follow-up.

Giant nasofrontal meningioma: endoscopic and transcranial approach followed by microvascularized vastus laterallis flap reconstruction.

A 12-year-old girl presented with headache, nasal voice, and anosmia. Magnetic resonance imaging demonstrated a 11 × 9 × 8-cm tumor extending from the nasal cavity to the frontal lobes. Histological analysis was consistent with transitional meningioma WHO grade I. As far as we know, this is the first reported case of a giant olfactory groove meningioma invading the nasal cavity through the anterior cranial base. Complete surgical removal was accomplished with excellent result via a staged endoscopic and transcranial approach. A microvascularized vastus laterallis flap was used for reconstruction. Surgical options and technical details in the management of this lesion are reviewed.

Postoperative epidural hematoma contributes to delayed upper cord tethering after decompression of Chiari malformation type I.

BACKGROUND: Symptomatic arachnoiditis after posterior fossa surgical procedures such as decompression of Chiari malformation is a possible complication. Clinical presentation is generally insidious and delayed by months or years. It causes disturbances in the normal flow of cerebrospinal fluid and enlargement of a syrinx cavity in the upper spinal cord. Surgical de-tethering has favorable results with progressive collapse of the syrinx and relief of the associated symptoms. CASE DESCRIPTION: A 30-year-old male with Chiari malformation type I was treated by performing posterior fossa bone decompression, dura opening and closure with a suturable bovine pericardium dural graft. Postoperative period was uneventful until the fifth day in which the patient suffered intense headache and progressive loose of consciousness caused by an acute posterior fossa epidural hematoma. It was quickly removed with complete clinical recovering. One year later, the patient experienced progressive worsened of his symptoms. Upper spinal cord tethering was diagnosed and a new surgery for debridement was required. CONCLUSIONS: The epidural hematoma compressing the dural graft against the neural structures contributes to the upper spinal cord tethering and represents a nondescribed cause of postoperative fibrosis, adhesion formation, and subsequent recurrent hindbrain compression.