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Biomedical subjects

H E Kaeser

Publications and source records attributed to H E Kaeser.

At least 19 recordsLinked to original sources

Muscle damping measured with a modified pendulum test in patients with fibromyalgia, lumbago, and cervical syndrome.

STUDY DESIGN: Muscle tension with tenderness may be localized or generalized as in fibromyalgia. Wartenberg's pendulum test might be appropriate for quantitating muscle damping, at least in generalized cases. OBJECTIVE: Damping values provide a quantitative measure of muscle tension and of the response to various treatments. SUMMARY OF THE BACKGROUND DATA: According to recent anatomic and experimental works, intrafusal muscle fibers are double-innervated by gamma motoneurons and sympathetic fibers. With electromyograph recording, the activity of extrafusal fibers and gamma motoneurons (reflexes) can be assessed and separated from the action of the sympathetic system. METHODS: An electrogoniometer registers the movements of the freely swinging leg. On the oscilloscope, the patient's nodular curve is compared with an ideal calculated dampened curve to find the damping value. Electromyograph surface electrodes from the knee extensors and flexors detect the activity of extrafusal fibers and the occurrence of reflexes. RESULTS: In longstanding severe fibromyalgia, damping values are almost always elevated, at least in one leg. Half or more of patients with chronic lumbago and cervical syndrome present with increased damping. The surface electromyograph remains silent (in contrast to spastic patients). CONCLUSION: The findings support the hypothesis that muscle tension in rheumatic patients results from overactivity of the sympathetic system (or part of it). Even in clinically localized pain syndromes, muscle damping is often increased in the legs. The test is valuable for quantitating muscle tension and the effectiveness of therapeutic methods.

Adult

[Polyneuropathies with an abnormal tendency for pressure-induced paralysis].

A 52-year old man is discussed. At age of 14 he was noticed to have pes cavus and thin shanks on both sides und drop foot on the right side. Since that time he has been suffering from episodic sensory loss in the distribution of the ulnar, median, peroneal and trigeminal nerves. An extended sensory loss around the pelvis and the posterior aspect of the thighs was a rather unique feature in this patient. As the patient refused nerve biopsy it cannot be decided whether peroneal muscular atrophy with multiple nerve compressions or if the entity of polyneuropathy with liability to pressure palsies was present.

Diagnosis, Differential

[Rare form of uveitis with neurological symptoms: the Vogt-Koyanagi-Harada uveomeningoencephalitic syndrome].

A 51-year-old Italian woman developed migraine-like headaches with increasing frequency 5 years after menopause. The simultaneous onset of severe bilateral uveitis, neurological signs such as vertigo, hearing loss, small sensomotor hemisyndrome, cognitive brain dysfunction and lymphocyte liquor pleocytosis confirmed the diagnosis of Vogt-Koyanagi-Harada syndrome, a rare disease of probably autoimmune origin with destruction of pigment containing neuroepithelium. Other vasculitic diseases, especially those of infectious or rheumatologic origin, were excluded. Systemic corticoid treatment suppressed the activity of the illness but on dose reduction relapses occurred. Additional immunosuppressive medication prevented uveitic relapses and made it possible to reduce the corticoid dose.

Cyclophosphamide