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1.
Artículo en Inglés, Ruso | MEDLINE | ID: mdl-26528613

RESUMEN

AIM: The study objective was to summarize our own experience of surgical treatment of spina bifida in adults. MATERIAL AND METHODS: The mean age of patients was 33 years. The time elapsed since the onset of clinical presentations till surgery varied from 11 to 14 years. Among all elective, surgically significant pathologies of the spinal cord (tumors, syringomyelia, arachnoid cysts, spontaneous epidural hematoma, epidural abscess, abscess), spina bifida in adults amounted to 5.9%. RESULTS: The level of social adaptation of patients at the time of diagnosis was quite acceptable (patients had a normal index of intellectual development and the ability to move). The amount of surgery was large and included implementation of several important surgical manipulations. The operative time was 5.5 h, on average. As a result, the spinal cord and its roots were released from compression and retaining structures that, to some extent, allowed for avoiding dissection of the terminal ligament. CONCLUSION: Minimally invasive technologies can not still ensure implementation of all surgical manipulations for correction of the vertebral-medullary anomaly. Surgical treatment of congenital anomalies of the spinal cord in adults proved to be reasonable and effective.


Asunto(s)
Procedimientos Neuroquirúrgicos/métodos , Disrafia Espinal/cirugía , Adulto , Electromiografía , Femenino , Humanos , Imagen por Resonancia Magnética , Masculino , Disrafia Espinal/diagnóstico , Resultado del Tratamiento
2.
Artículo en Inglés, Ruso | MEDLINE | ID: mdl-25909748

RESUMEN

A clinical case of a 12 year-old girl with hydrocephalus complicated by rare condition, lateral ventricular diverticulum, is reported. Progression of the diverticulum was followed up according to MRI. The diverticulum of the lateral ventricular wall has emerged in the interval of 1 year (14 months have passed between the two MRI examinations) and spread towards the quadrigeminal cistern. In addition, compression of cerebellum, aqueductus cerebri Sylvii, and the fourth ventricle of the brain have emerged. A surgical treatment was suggested after the hydrocephalus had been initially revealed (when the diverticulum had not been formed yet); however, the child's parents refused the therapy. One year later, a series of epileptic seizures emerged, and MR scans showed a cystic neoplasm in the postcranial fossa above the cerebellum. The genesis of the cyst and its nature were unclear and additional invasive examination methods were required. MSCT ventriculography confirmed the diverticulum of the right lateral ventricle towards the quadrigeminal cistern.


Asunto(s)
Quistes Aracnoideos , Ventriculografía Cerebral , Hidrocefalia , Ventrículos Laterales/diagnóstico por imagen , Imagen por Resonancia Magnética , Quistes Aracnoideos/diagnóstico por imagen , Quistes Aracnoideos/etiología , Niño , Femenino , Humanos , Hidrocefalia/complicaciones , Hidrocefalia/diagnóstico por imagen
3.
Zh Vopr Neirokhir Im N N Burdenko ; 77(1): 46-52; discussion 52, 2013.
Artículo en Inglés, Ruso | MEDLINE | ID: mdl-23659120

RESUMEN

Sixty-two year old man was admitted to the department of neurosurgery after stroke episode. CT-scan revealed non-traumatic, non-hypertensive intracerebral hemorrhage in the left temporal lobe; cerebral amyloid angiopathy was suspected. Initially, according to Boston criteria, intracerebral hematoma was interpreted as a result of a "probable" cerebral amyloid angiopathy. Surgical evacuation of the hematoma lead to the partial recourse of speech and cognitive deficit. Four weeks after stroke onset and 3 weeks after surgery CT was performed, which revealed intracerebral hematoma in the right parietal lobe; this fact let to diagnose "probable" cerebral amyloid angiopathy. The second hematoma was evacuated, and surgical treatment together with medical therapy improved patient's quality of life. Treatment strategy for the intracerebral hematomas resulting from cerebral amyloid angiopathy has not been justified yet, which requires further investigations.


Asunto(s)
Angiopatía Amiloide Cerebral/diagnóstico , Hemorragias Intracraneales/cirugía , Angiopatía Amiloide Cerebral/complicaciones , Angiopatía Amiloide Cerebral/psicología , Humanos , Hemorragias Intracraneales/diagnóstico , Hemorragias Intracraneales/etiología , Hemorragias Intracraneales/psicología , Angiografía por Resonancia Magnética , Masculino , Persona de Mediana Edad , Tomografía Computarizada Multidetector , Procedimientos Neuroquirúrgicos/métodos , Calidad de Vida , Resultado del Tratamiento
4.
Zh Vopr Neirokhir Im N N Burdenko ; (4): 41-7; discussion 47-8, 2010.
Artículo en Ruso | MEDLINE | ID: mdl-21374936

RESUMEN

The paper describes a case of treatment of 4-year old male patient with rare combination of 2 intracranial arachnoid cysts with hydrocephalus. First surgery (VP-shunt) was performed in the age of 10 months. 3 years later decompensation resulted in seizures. Detailed non-invasive visualization of intracranial CSF compartments was achieved by multispiral CT scans. Selection of surgical treatment was complicated. Reoperation and atypical shunting resulted in balanced relationships of intracranial volumes and steady clinical improvement.


Asunto(s)
Quistes Aracnoideos/cirugía , Hidrocefalia/cirugía , Quistes Aracnoideos/complicaciones , Quistes Aracnoideos/diagnóstico por imagen , Preescolar , Craniectomía Descompresiva/efectos adversos , Humanos , Hidrocefalia/complicaciones , Hidrocefalia/diagnóstico por imagen , Masculino , Complicaciones Posoperatorias/diagnóstico por imagen , Complicaciones Posoperatorias/cirugía , Radiografía , Convulsiones/diagnóstico por imagen , Convulsiones/etiología , Convulsiones/cirugía
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