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Biomedical subjects

D C Preston

Publications and source records attributed to D C Preston.

At least 19 recordsLinked to original sources
PubMed2001

Localization of ulnar neuropathy with conduction block across the elbow.

We performed short segment incremental stimulation on 13 consecutive patients with ulnar neuropathy across the elbow (UNE) and conduction block. Conduction block occurred proximal to the medial epicondyle in 62%, at the epicondyle in 23%, and below the elbow in 15%. The ulnar nerve may be more prone to external compression above the elbow than previously recognized. Short segment incremental studies are useful to identify conduction block above the elbow in such patients.

Action Potentials↗
PubMed1999

Amplitude-dependent slowing of conduction in amyotrophic lateral sclerosis and polyneuropathy.

The mechanism of motor nerve conduction slowing in amyotrophic lateral sclerosis (ALS) is thought primarily to be loss of large, fast-conducting motor fibers; this is less certain in axonal polyneuropathy. We compared motor conduction studies in 64 patients with axonal polyneuropathy with 72 patients with ALS. Compound motor action potential amplitude, distal motor latency, and conduction velocity were converted to a percentage of the upper or lower limit of normal and then represented as a square root (SQRT) transformation, plotted with SQRT amplitude as the independent variable and SQRT latency or SQRT conduction velocity as the dependent variables. Regression analysis of the lower extremity nerve data showed that prolongation of latency and slowing of velocity were amplitude-dependent and were virtually identical in ALS and polyneuropathy. In the upper extremity, amplitude-dependent prolongation of latency was similar in both groups, but amplitude-dependent slowing of velocity was seen in ALS and not in axonal polyneuropathy. Our data support the hypothesis that the major mechanism of slowing is similar in both polyneuropathy and ALS and is the loss of large, fast-conducting fibers. However, the presence of distal but not proximal slowing in the upper extremity of axonal polyneuropathy suggests that additional mechanisms may be contributory.

Action Potentials↗
PubMed1999

Distal median neuropathies.

Distal median neuropathy is the most common entrapment neuropathy affecting the upper extremity. Although most often idiopathic, there are a large number of associated medical disorders. Electrophysiologic testing plays a central role in the diagnosis of distal median neuropathy in establishing localization; assessing severity; and excluding disorders of the proximal median nerve, plexus, and nerve roots which can mimic the clinical symptoms of distal median neuropathy. Treatment is usually successful, especially when diagnosis is established early in the course before any significant axonal loss has occurred.

Carpal Tunnel Syndrome↗
PubMed1998

Short-segment incremental studies to localize ulnar nerve entrapment at the wrist.

Precise electrophysiologic localization of ulnar neuropathy at the wrist (UNW) is often problematic. In the last year, we evaluated only two patients who presented clinically with UNW. Routine electrophysiologic techniques were nondiagnostic for UNW. In contrast, short-segment incremental studies (SSIS) across the wrist demonstrated conduction block and segmental slowing of nerve conduction across the wrist in both patients. We conclude that SSIS is a valuable tool for diagnosis, precise localization, and prognosis of UNW.

Adult↗
PubMed1997

A case of Hodgkin's lymphoma producing neuromyotonia.

The syndrome of neuromyotonia produces muscle stiffness, cramps, and frequently, excessive sweating. Most cases are idiopathic, but some are associated with neoplasms, especially immune cell cancers. Voltage-gated potassium channels may be the target of an autoantibody attack in idiopathic generalized neuromyotonia (Isaacs' syndrome). The cases associated with neoplasms may also have an autoimmune etiology. We report the first case of neuromyotonia as the presenting feature of Hodgkin's lymphoma and propose a paraneoplastic mechanism that would link the purported autoimmune etiology in Isaacs' syndrome with the cancer-associated cases.

Adult↗
PubMed1996

Lumbrical-interossei motor studies localize ulnar neuropathy at the wrist.

Ulnar nerve entrapment at the wrist (UNW) is uncommon and often difficult to localize electrophysiologically. The difference between the motor latencies to the median-innervated second lumbrical (2L) and ulnar-innervated palmar interosseous (Pl) (Diff 2L-Pl) has been shown to be of localizing value in patients with median neuropathy at the wrist. In the last year, we evaluated 2 patients with clinically definite ulnar neuropathy at the wrist. We performed motor studies to the 2L-Pl on the 2 patients and 12 disease controls with ulnar neuropathy at the elbow as follows: Using the same electrodes to record both the 2L and Pl, the median and ulnar nerves were each stimulated supramaximally above the wrist using identical distances. In the disease control subjects, the Diff 2L-Pl was essentially the same as normal controls (mean [0.13], range [(-0.3)-0.4]). In both patients with UNW, the Diff 2L-Pl clearly supported the routine electrophysiological studies in localizing the lesion (ulnar latencies were 1.1 and 1.8 ms longer than the median latencies). We conclude that the lumbrical-interosseous latency difference is useful in localizing ulnar nerve entrapment to the wrist.

Adult↗
PubMed1996

Myotonia in colchicine myoneuropathy.

Colchicine may induce a myoneuropathy in patients with renal insufficiency. To date, myotonia has not been described in this disorder. We recently studied 4 patients treated with routine doses of colchicine who, in the setting of renal insufficiency, developed a severe myoneuropathy characterized by prominent myotonic discharges on electromyography. In addition, 1 of the 4 patients had profound clinical myotonia. In the 3 patients in whom biopsies were performed, marked myopathic change with intracytoplasmic vacuolization was identified. All 4 patients improved rapidly with discontinuation of the medication. The patient in whom electrophysiologic studies were repeated had a complete resolution of the myotonic discharges. Colchicine myoneuropathy can present with prominent clinical and electrophysiologic myotonia that resolves completely with discontinuation of the medication.

Adult↗
PubMed1996

Dystonic postures generated from complex repetitive discharges.

We report a woman with a chronic inflammatory myopathy who developed muscle stiffness and dystonic postures of both upper extremities. Electromyography demonstrated that involuntary complex repetitive discharges of muscle caused the posture. Rare cases of dystonic posturing may be of peripheral, and not central system, origin.

Dystonia↗
PubMed1996

Activity-dependent conduction in single motor units.

Vertebrate sensory and motor axons vary in their responses to submaximal stimuli as a function of time since prior activation. When two equal but submaximal stimuli are presented in pairs, the response to the second stimulus may be greater or less than the response to the first stimulus, depending on the interstimulus interval (ISI). We studied both the supernormal period (ISI between 6 and 25 msec) and the subnormal period (ISI between 25 and 100 msec) under conditions where only single motor axons were stimulated. Twenty single motor units from eight normal subjects were studied. The behavior of single units was very similar to that observed in compound motor action potentials, with the supernormal period lasting approximately 20 msec, followed by a subnormal period lasting at least 80 msec. Surprisingly, a supernormal period could be evoked by a stimulus that did not produce a response in the motor unit being studied; however, the presence of subnormality was dependent on an action potential being generated in response to the first stimulus. Based on these results, we conclude that the supernormal period does not require the opening of voltage-dependent ion channels, in contrast to the later occurring subnormal period.

Action Potentials↗
PubMed1996

Delayed radiation-induced bulbar palsy.

We report a man with a slowly progressive bulbar palsy 14 years after radiation therapy for nasopharyngeal carcinoma. Electromyography demonstrated prominent myokymic and neuromyotonic discharges in muscles innervated by the lower cranial nerves. Late effects of radiation therapy can occur in the cranial nerve musculature that are similar to well-recognized syndromes affecting the brachial plexus and spinal cord.

Adult↗
PubMed1996

Paraspinal muscle hematoma after electromyography.

There have been few reports of complications related to electromyography. Needle examination of certain muscles is sometimes avoided in patients taking anticoagulant agents, although no clear guidelines have been established. We describe a patient who was not receiving an anticoagulant and developed a large paraspinal muscle hematoma after routine electromyography. Subsequently, all patients who underwent paraspinal muscle electromyography and were diagnosed with radiculopathy at our institution over a 14-month period were reviewed. From this group, 17 patients were identified who had also underwent MRI of the appropriate spinal levels within 1 week after the needle examination. These images were reviewed for evidence of paraspinal muscle hematomas. Four small hematomas were identified in four different patients. None of these were radiologically significant compared with the large hematoma described in the case report. Radiologically apparent paraspinal hematomas after electromyography are an unusual complication of needle examination and do not appear to have any clinical significance. Nevertheless, the presence of these lesions justifies caution when considering electromyography of paraspinal and other deeper muscles in anticoagulated patients.

Adult↗