Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 3 de 3
Filtrer
Plus de filtres








Gamme d'année
1.
Neurol India ; 2003 Sep; 51(3): 379-82
Article de Anglais | IMSEAR | ID: sea-121768

RÉSUMÉ

We report two cases of posterior third ventricular choroid plexus papilloma, one in an 8-month-old infant and another in a two-year-old child. These cases presented with features of obstructive hydrocephalus. Both these patients underwent a ventriculo-peritoneal (VP) shunt surgery prior to the tumor excision. Following the VP shunt surgery both patients developed ascitis requiring exteriorization of the abdominal end of the shunt. There was a clear proof of CSF overproduction: 1400-1500 ml/day in the eight-month-old infant and 900-1200 ml/day in the two-year-old child. In the former it was transient and could be treated with revision of the VP shunt whereas in the second case a ventriculo-arterial shunt had to be done. In the second case a staged reduction cranioplasty was also performed for an enormously enlarged head (head circumference--74 cm). Interesting clinical and radiological findings and useful management strategies are described.


Sujet(s)
Tumeurs des ventricules cérébraux/complications , Enfant d'âge préscolaire , Femelle , Humains , Hydrocéphalie/étiologie , Nourrisson , Mâle , Papillome du plexus choroïde/complications , Troisième ventricule , Dérivation ventriculopéritonéale
2.
Neurol India ; 2001 Dec; 49(4): 395-7
Article de Anglais | IMSEAR | ID: sea-120336

RÉSUMÉ

Yolk sac tumours are rare conditions among the germ cell tumours. Intracerebral germ cell tumours are exceedingly rare. A 15 year old girl presenting with a one week history of raised intracranial pressure is described. She had bilateral papilloedema and a right 6th nerve palsy. CT scan showed an intra-parenchymatous right frontal ring enhancing lesion of 2 cms diameter. The patient underwent microsurgical total excision of the tumour, followed by chemotherapy. She was asymptomatic at three years following surgery.


Sujet(s)
Adolescent , Protocoles de polychimiothérapie antinéoplasique/usage thérapeutique , Bléomycine/usage thérapeutique , Tumeurs du cerveau/traitement médicamenteux , Cisplatine/usage thérapeutique , Association thérapeutique , Tumeur du sac vitellin/traitement médicamenteux , Femelle , Lobe frontal , Humains , Microchirurgie , Tomodensitométrie , Vinblastine/usage thérapeutique
3.
Neurol India ; 2001 Jun; 49(2): 188-90
Article de Anglais | IMSEAR | ID: sea-121834

RÉSUMÉ

Malignant peripheral nerve sheath tumour (MPNST) is a rare malignant neoplasm arising from the supportive non-neural component of the peripheral nerves. An unusual case of pain and weakness of the foot and calf muscles due to a giant MPNST of the sciatic nerve in the posterior compartment of the thigh is presented. The patient was already investigated as a case of sciatica due to a lumbar disc disease with a negative magnetic resonance imaging and then unsuccessfully operated elsewhere twice, with a misdiagnosis of tarsal tunnel syndrome. Neurosurgical referral prompted a diagnostic magnetic resonance study of the thigh, revealing the lesion, which was completely excised microsurgically with total relief in the pain and partial improvement in the weakness and sensations in the sole of the foot.


Sujet(s)
Adulte , Femelle , Humains , Imagerie par résonance magnétique , Microchirurgie , Tumeurs des gaines nerveuses/complications , Tumeurs du système nerveux périphérique/complications , Nerf ischiatique , Sciatalgie/étiologie , Cuisse/innervation
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE