Search PubMed⌕ Search

Biomedical subjects

T Jaspan

Publications and source records attributed to T Jaspan.

At least 37 records · Page 2Linked to original sources
PubMed1999

Brown-Sequard syndrome after management of vertebral hemangioma with intralesional alcohol. A case report.

STUDY DESIGN: This report describes Brown-Sequard syndrome after intralesional injection of absolute alcohol into vertebral hemangioma. OBJECTIVE: To discuss whether the described technique is safe in the management of vertebral hemangiomas. SUMMARY OF BACKGROUND DATA: The management of vertebral hemangiomas remains controversial. There have been reports of successful management using intralesional absolute alcohol. METHODS: The clinical and radiologic features of the reported complication are detailed. RESULTS: Intralesional injection of absolute alcohol caused Brown-Sequard syndrome. CONCLUSION: This case shows that intralesional alcohol injection cannot be considered a safe technique for management of vertebral hemangiomas with spinal cord compression.

Adult↗
PubMed1999

Cerebellar encephalomalacia on magnetic resonance imaging after removal of acoustic tumor.

MRI is widely used for postoperative surveillance of patients undergoing surgery for removal of acoustic neuroma. The purpose of this study was to investigate the frequency and pattern of postoperative changes in the cerebellum and brain stem on MRI after removal of acoustic neuroma. A retrospective study was conducted in 30 consecutive patients who underwent postoperative MRI between 1994 and 1995. The timing of the scans after surgery ranged from 12 months to 10 years. T2 -weighted turbo spin-echo images revealed cerebellar encephalomalacia in 17 of 30 cases. Cerebellar encephalomalacia was found more consistently in patients who had large tumors and was more frequent after the suboccipital approach. Encephalomalacia is largely caused by gliotic changes in the adjacent cerebellar tissues after tumor removal.

Adolescent↗
PubMed1999

Anaesthesia for caesarean section in a patient with recent subarachnoid haemorrhage and severe pre-eclampsia.

Subarachnoid haemorrhage is a leading 'indirect' cause of maternal death in the UK. We describe the case of a 43-year-old woman who presented with headache, photophobia and neck stiffness of sudden onset at 32 weeks' gestation. Cerebral computed tomography demonstrated subarachnoid blood in the cisterns around the midbrain, and oral nimodipine was started to prevent vasospasm. Preparations were made for endovascular coil embolisation in the event of identification of a posterior circulation aneurysm. However, angiography under general anaesthesia failed to reveal any vascular abnormality. On emergence from anaesthesia, headache persisted, and over the next 24 h severe pre-eclampsia developed. Magnesium sulphate was started, and urgent Caesarean section performed under general anaesthesia without incident. The rationale for the neuroradiological, obstetric and anaesthetic management is discussed.

Adult↗
PubMed1999

Coil embolization of cerebral aneurysms in patients with sickling disorders.

In patients with sickle cell disease cerebral aneurysm formation is thought to be a complication of recurrent red cell sickling, and multiple aneurysms have been reported in these patients. Management of patients with suspected cerebral aneurysm has traditionally involved cerebral vessel angiography followed by craniotomy and aneurysmal clipping. In patients without sickle cell disease, non-operative intervention in the form of endovascular coil embolization is increasingly being used to ablate aneurysms, but has not thus far been reported in patients with sickle cell disease. We report two patients with sickling disorders who have undergone coil embolization of cerebral aneurysms with good functional and radiological outcomes. These patients illustrate that endovascular coiling is useful in the treatment of cerebral aneurysms associated with sickling disorders, although, as with surgical intervention, preparation with exchange transfusion is appropriate.

Adult↗
PubMed1999

Infratentorial atrophy on magnetic resonance imaging and disability in multiple sclerosis.

Loss of tissue volume in the central nervous system may provide an index of fixed neurological dysfunction in multiple sclerosis. Recent magnetic resonance studies have shown a modest relationship between clinical disability rating scores and transverse sectional area of the cervical spinal cord. To explore further the relationship between atrophy and disability in multiple sclerosis, we estimated the volumes of infratentorial structures from MRIs in a cross-sectional study of 41 patients, 21 with relapsing-remitting multiple sclerosis and 20 with secondary progressive multiple sclerosis. We used the Cavalieri method of modern design stereology with point counting to estimate the volume of brainstem, cerebellum and upper cervical spinal cord from three-dimensional MRIs acquired with an MPRAGE (Magnetization-prepared Rapid Acquisition Gradient Echo) sequence. The volume of the upper (C1-C3) cervical spinal cord was significantly correlated with a composite spinal cord score derived from the appropriate Functional Scale scores of the Expanded Disability Status Scale (r = -0.50, P < 0.01). The cerebellar (r = 0.49, P < 0.01) and brainstem (r = 0.34, P < 0.05) volumes correlated with the Scripp's Neurological Disability Rating Scale scores. The upper cervical cord volumes (r = -0.39, P < 0.01), but not the brainstem or cerebellar volumes, were significantly associated with disease duration. MRI-estimated structural volumes may provide a simple index of axonal and/or myelin loss, the presumed pathological substrates of irreversible impairment and disability in multiple sclerosis.

Activities of Daily Living↗
PubMed1998

Idiopathic diffuse erosion of the skull base presenting as cerebrospinal fluid rhinorrhoea.

We present an unusual case of generalized erosion of the skull base. We have not found a similar case reported in the world literature. The presenting symptom was spontaneous cerebrospinal fluid (CSF) rhinorrhoea which arose from a bony defect associated with herniation of the right temporal lobe into the sphenoid sinus. We discuss the management of such a case including imaging of the skull base and the endoscopic repair of the bony defect.

Aged↗
PubMed1997

Neuro-endoscopic third ventriculostomy: evaluation with magnetic resonance imaging.

We have performed a prospective study of the use of magnetic resonance (MR) imaging in 14 patients undergoing neuro-endoscopic third ventriculostomy. MR imaging was undertaken prior to the endoscopy and serial studies were carried out after the procedure. MR imaging provides important information concerning the morphology of the third ventricle and allows the identification of an appropriate puncture site in the floor of the third ventricle. In particular, the relationship of the third ventricular floor to the basilar artery is well demonstrated. Following an endoscopic septostomy, MR imaging allows visualisation of any change in ventricular size. A cerebro-spinal fluid (CSF) flow void in the anterior inferior third ventricle, sometimes extending into the suprasellar cisterns was frequently demonstrated and this was found to be a more constant feature than reduction in ventricular size. MR imaging provides an indispensable tool for both planning and follow-up of endoscopic third ventriculostomy.

Basilar Artery↗
PubMed1996

Comparison of magnetic resonance angiography with conventional angiography in the detection of intracranial aneurysms in patients presenting with subarachnoid haemorrhage.

Thirty-nine patients admitted with proven subarachnoid haemorrhage were imaged both with 3-D time of flight (TOF) magnetic resonance angiography (MRA) and conventional angiography. As the definitive examination, catheter angiography demonstrated 37 aneurysms; ten patients had no aneurysm, the remaining 29 patients had 37 aneurysms. We found the sensitivity of 3-D TOF MRA for the detection of aneurysms to be 81% and specificity to be 100% when the reporting radiologist inspects not only the MIP reconstructions but also the MRA source data and the axial spin-echo images. The investigation is less accurate if all the available imaging data is not considered.

Adult↗
PubMed1995

Problems and pitfalls of 3-D TOF magnetic resonance angiography of the intracranial circulation.

3-D Time of flight (TOF) Magnetic resonance angiography (MRA) is being increasingly adopted as a technique for assessment of the intracranial circulation in neuroradiological practice. We describe our recent experience of 3-D time of flight Magnetic resonance angiography. We describe some of the problems and potential pitfalls that we have experienced employing 3-D TOF MRA in these circumstances, and the diagnostic dilemmas that have arisen. A range of problems have been encountered. When performing 3-D TOF MRA, other phenomena such as sub-acute thrombus and high signal structures may be incorporated into the Maximal Intensity Projection (MIP) reconstruction and masquerade as vascular abnormalities. Interpretation of MIP reconstructions can also be difficult or impossible in the presence of sizeable haematoma. Conversely, vascular structures may not be appreciated because of loss of signal from saturation effects or dephasing due to slow or complex flow. Local susceptibility artefacts, from aneurysm clips or coils, may reduce the signal from vascular structures. Interpretation of 3-D TOF MRA must take account of potential pitfalls which can be minimized by adoption of appropriate imaging and review strategies. This requires careful consideration of MRA source data, the spin-echo axial images as well as the MIP reconstructions.

Adult↗
PubMed1995

Detecting deletions in the critical region for lissencephaly on 17p13.3 using fluorescent in situ hybridisation and a PCR assay identifying a dinucleotide repeat polymorphism.

During a study of lissencephaly in England and Wales, 23 children were identified with this diagnosis. They were classified as follows: three children had Miller-Dieker syndrome (MDS), 13 had isolated lissencephaly sequence (ILS), two had type II lissencephaly, and five children were reclassified as focal or diffuse cortical dysplasia. Microdeletions of chromosome 17p13.3, also known as the Miller-Dieker critical region, have been associated with both MDS and ILS. We used the commercially available Oncor probe for fluorescent in situ hybridisation (FISH) studies on 14 patients and a further four were studied elsewhere. Deletions were identified in all three MDS patients and two of the ILS patients. These results are consistent with previously reported data. No deletions were found in those patients with focal or diffuse cortical dysplasia. In addition, a CA repeat polymorphism which maps to the Miller-Dieker critical region was studied in 12 families and was informative in nine; the results were consistent with the FISH data. We conclude that FISH is a reliable method to detect deletions in patients with MDS and ILS and also useful to identify chromosome rearrangements in their parents which are not detected by conventional cytogenetic analysis. The PCR assay, if informative, is also reliable and a useful alternative if only DNA is available. None of the five children with atypical radiological features had a deletion. We therefore suggest that as well as looking for other aetiologies a careful review of the diagnosis should be made of the MDS or ILS cases in whom a deletion is not found.

Brain↗