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Biomedical subjects

M H Silber

Publications and source records attributed to M H Silber.

29 records · Page 2Linked to original sources
PubMed1991

Carotid artery disease in young adults.

The angiographic and clinical findings in 17 young adults (14-39 years) with stenosis and/or occlusion of at least one of the common or internal carotid arteries were reviewed to determine the spectrum of carotid artery disease in this age group. Five aetiological groups were identified: atherosclerosis (3 patients), arteritis (4), non-inflammatory arteriopathies (6), compression by neoplasm (1), and occlusions of undetermined cause (3). Over a mean follow-up time of 19.7 months, 2 patients died (12.5%) and further cerebrovascular events occurred in 4 others (25%). We conclude that carotid angiography plays a meaningful role in providing a definitive diagnosis in young adults with carotid artery disease and thus may assist with therapy and prognosis.

Adolescent↗
PubMed1990

Idiopathic acute myelopathy.

The clinical spectrum of acute intrinsic spinal cord disease remains uncertain because of varying criteria used in different studies. The characteristics of 17 patients with idiopathic acute myelopathy drawn from a larger group of 34 with acute intrinsic myelopathies of varying aetiology are reported. Results, which differ from previous studies, include the finding of a high proportion of patients with evidence of predominantly unilateral cord disease (47%). A higher percentage of patients (24%) than previously reported later developed multiple sclerosis, possibly related to broader inclusion criteria. A rise in protein concentration of the cerebrospinal fluid on repeat lumbar puncture was observed in patients with spinal shock on presentation, and a poor outcome was most clearly associated with these cases.

Acute Disease↗
PubMed1990

The multiple sleep latency test in the diagnosis of sleep disorders.

The multiple sleep latency test provides an objective measure of a patient's daytime sleepiness. Sixteen tests were performed at Groote Schuur Hospital in 1987 and 1988 according to a fixed protocol. In 8 patients the test was definitely abnormal (mean sleep latency less than 5 minutes) with 3 subjects diagnosed as having narcolepsy, 1 sleep apnoea syndrome, 1 idiopathic central nervous system hypersomnolence, 2 environment-related hypersomnolence and 1 psychophysiological hypersomnolence. In 2 patients the test results fell in the equivocal range (mean sleep latency 5-10 minutes), while in 5 the test revealed no evidence for a disorder of excessive sleep (mean sleep latency greater than 10 minutes). The test was uninterpretable for technical reasons in only 1 patient. In conclusion, the test--when performed in a standardised manner--is extremely helpful in the elucidation of possible disorders of excessive sleep.

Adult↗
PubMed1990

Neuromyelitis optica (Devic's syndrome) and pulmonary tuberculosis.

Neuromyelitis optica and acute necrotic myelopathy occur in association with pulmonary tuberculosis. We studied 8 patients with either neuromyelitis optica (6), acute myelopathy (1), or acute optic neuropathy (1) in close temporal association with pulmonary tuberculosis, but with no evidence for CNS tuberculosis. Neurologic symptoms preceded the use of antituberculosis medication in 5 patients. Different patients showed similar clinical features, suggesting a consistent disease pattern. Autopsy examination (1 patient) revealed extensive spinal cord and optic nerve demyelination. We identified only 5 additional patients seen over the same period with idiopathic neuromyelitis optica, thus suggesting that the close temporal relationship to pulmonary tuberculosis is not coincidental. The syndrome is most likely due to an immune reaction to tuberculosis rather than the use of antituberculosis medication.

Adolescent↗
PubMed1989

Syphilitic myelopathy.

Whether the clinical pattern of neurosyphilis has changed since the introduction of penicillin is controversial. This study describes the clinical, laboratory and radiological features of nine patients with syphilitic myelopathy, to assess whether the disease pattern has changed in this subgroup. Four patterns based on clinical course and radiological findings were identified: three patients presented with subacute paraparesis, four with prodromal backache and/or mild leg weakness followed by sudden paraplegia, one patient developed slowly progressive weakness over 4 years and one patient who progressed over one month was shown to have dural thickening on myelography. All patients showed CSF pleocytosis with positive CSF VDRL in seven patients. Despite therapy the prognosis for recovery was not good. Compared with pre-penicillin era studies, the clinical pattern has not significantly changed. Greater alertness to the diagnosis might result in earlier therapy and thus possibly lead to improved prognosis.

Adult↗
PubMed1987

Vascular malformations of the posterior fossa. Clinical and radiologic features.

Thirty-one patients with vascular malformations of the posterior fossa were studied to determine their clinical presentation and radiologic diagnosis. The most common clinical presentations were acute hemorrhage (68%, 21/31) and progressive or fluctuating focal neurologic deficits resembling those found in other pathologic processes (19%, 6/31). Trigeminal neuralgia and hemifacial spasm occurred in these patients, but they were rarely initial presenting symptoms. Computed tomography, after infusion of contrast medium, was abnormal in 95% (20/21) of the patients. Angiography established or confirmed the diagnosis in most of the patients; however, a negative angiogram, especially in cases with recent hemorrhage, does not exclude the diagnosis.

Adolescent↗
PubMed1985

Beriberi heart disease. A case report describing the haemodynamic features.

Beriberi heart disease should be considered in all patients with cardiac failure and a history of alcohol abuse or dietary deficiency. We studied the haemodynamic changes which took place immediately after intravenous administration of thiamine to a patient with high-output beriberi. Cardiac output and stroke volume fell rapidly, but not below normal levels, and systemic vascular resistance rose.

Adult↗
PubMed1983

Acute transverse myelopathy in Epstein-Barr virus infection. Case reports.

Two patients with acute transverse myelopathy in association with Epstein-Barr virus infection are described. Evidence of Epstein-Barr virus infection should be sought in any young patient with an acute neurological illness, even in the absence of the usual features of infectious mononucleosis. The cases described confirm previous reports that the prognosis in patients with neurological complications of this infection is generally good.

Acute Disease↗