ABSTRACT
Despite the introduction of local thrombolytic therapy, there is still a very high mortality rate in basilar thrombosis. We report three cases of successful intra-arterial thrombolysis of acute basilar artery occlusion and consecutive interventional endovascular therapy. In all cases, the acute thrombosis of the basilar artery probably developed from preexisting atherosclerotic stenoses. The clinical outcomes were excellent. We discuss early consecutive stenting as a possible therapeutic option in cases of residual stenosis after successful intra-arterial lysis of basilar artery occlusion.
Subject(s)
Basilar Artery/surgery , Blood Vessel Prosthesis , Intracranial Thrombosis/surgery , Stents , Thrombolytic Therapy/methods , Vascular Surgical Procedures/instrumentation , Vascular Surgical Procedures/methods , Vertebrobasilar Insufficiency/surgery , Humans , Intracranial Thrombosis/etiology , Male , Middle Aged , Reoperation , Treatment Outcome , Vascular Surgical Procedures/adverse effects , Vertebrobasilar Insufficiency/diagnosis , Vertebrobasilar Insufficiency/therapyABSTRACT
In order to compare the sensitivity of multichannel derived median nerve SEP with EEG in vascular cerebral lesions we examined 22 normals and 23 patients. SEP components within the first 50 ms could be divided into main waveform patterns: (1) a W-shaped parietal pattern consisting of N20, P25, N35 and P45 in most cases. (2) a frontal pattern with P20 and N30 as well as possibly detectible N24, P28, P33, N40 and P50. (3) a central P22. Two younger normals showed a V-shaped parietal pattern with N20 and P35, a frontal pattern with P20 and N36, and central P22 with a remarkably long latency. All components could be analysed sufficiently by means of three representative electrode positions (stimulation right/left): P3/P4, C3/C4, and F3/F4, which reduces the expense of recording and analysing considerably. 21 patients (91.3%) showed abnormal results in SEP, whereas 14 patients (60.9%) in EEG. A three channel electrode array can increase the usefulness of SEP and detect cerebral dysfunctions in cerebral lesions in spite of normal EEG under routine examination conditions. Analysis of multichannel derived SEPs during treatment and recovery after stroke and search for the prognostic value in the acute stage of the disease should be done in future.
Subject(s)
Electroencephalography , Evoked Potentials, Somatosensory/physiology , Median Nerve/physiopathology , Stroke/physiopathology , Adult , Aged , Aged, 80 and over , Brain Mapping , Cerebral Cortex/physiopathology , Female , Humans , Male , Middle Aged , Reaction Time/physiology , Reference Values , Stroke/diagnosisABSTRACT
HISTORY AND ADMISSION FINDINGS: A 54-year-old woman with type 1 diabetes of about 2 years' duration developed painful cramps in the muscles of the abdominal wall, the back and the thighs. On admission physical examination confirmed markedly increased tone of the muscles of the trunk and those proximal to it. INVESTIGATIONS: Markedly increased amounts of anti-GAD (glutamic acid decarboxylase) antibodies were present in both serum and cerebrospinal fluid (CSF). Electroneurography and -myography revealed mild polyneuropathy but no other neurological abnormality. DIAGNOSIS, TREATMENT AND COURSE: Suspected stiff-man syndrome (SMS) was confirmed by the increased anti-GAD antibodies and the marked improvement on gradually increasing doses of clonazepam. The autoimmune syndrome affected several organ systems: central nervous system (SMS), pancreas (diabetes), thyroid (immuno-thyroiditis). Immunosuppressive treatment with azathioprine was begun. The patient remains in good general condition 22 months after the initial diagnosis, and there have been no new organ involvement. CONCLUSION: It is important to include SMS in the differential diagnosis, even though the symptoms are not those of the full-blown picture of this rare disease. Absence of muscle cramps and myoclonus but presence of depressive symptoms can easily result in misdiagnosis, preventing early initiation of effective symptomatic treatment.
