Diffuse large B-cell lymphoma presenting as piriformis syndrome.

Abstract:

:Piriformis syndrome (PS) is a rare condition characterized by pain and paresthesia of the buttock, often radiating to the posterior thigh. A patient with sciatica that was clinically suspicious for PS, underwent diagnostic work-up. A diagnosis of diffuse large B-cell lymphoma with neurolymphomatosis (NL) was made. To our knowledge, this is the first report of NL presenting as PS. NL is a possible cause of secondary PS.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Ye BS,Sunwoo IN,Suh BC,Park JP,Shim DS,Kim SM

doi

10.1002/mus.21538

subject

Has Abstract

pub_date

2010-03-01 00:00:00

pages

419-22

issue

3

eissn

0148-639X

issn

1097-4598

journal_volume

41

pub_type

杂志文章
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    abstract::The lack of effective therapy for many of the chronic neuromuscular diseases such as amyotrophic lateral sclerosis, hereditary motor sensory neuropathy (Charcot-Marie-Tooth disease), spinocerebellar degenerations and idiopathic polyneuropathy has led to a search for substances that may stimulate peripheral nerve regen...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.880130910

    authors: Bradley WG

    更新日期:1990-09-01 00:00:00

  • Hemolytic anemia associated with intravenous immunoglobulin.

    abstract::Intravenous immunoglobulin (IVIg) is a useful tool in the treatment of a variety of neuromuscular disorders. Though IVIg therapy is generally safe, hemolytic anemia is a potentially serious complication that is often overlooked, and is currently not listed in product inserts. We analyzed 45 patients who received IVIg ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199709)20:9<1142::aid-mus8

    authors: Wilson JR,Bhoopalam H,Fisher M

    更新日期:1997-09-01 00:00:00

  • Doxorubicin chemomyectomy as a treatment for cervical dystonia: histological assessment after direct injection into the sternocleidomastoid muscle.

    abstract::The sternocleidomastoid muscle (SCM) is one of the major muscles involved in producing abnormal head position in cervical dystonia patients. This study tested whether doxorubicin chemomyectomy, direct injection of doxorubicin into the SCM to permanently remove muscle fibers, has the potential to be a nonsurgical, perm...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199811)21:11<1457::aid-mus

    authors: McLoon LK,Falkenberg JH,Dykstra D,Iaizzo PA

    更新日期:1998-11-01 00:00:00

  • The influence of skeletal muscle reinnervation on experimentally induced myotonia.

    abstract::Earlier studies have shown that prior denervation of muscle prevents myotonia induced by 2,4-dichlorophenoxy acetic acid (2,4-D) both in vivo and in vitro. This work studied the effect of reinnervation on 2,4-D myotonia. Twenty Sprague-Dawley rats were injected with 2,4-D at specific intervals following unilateral sci...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880090414

    authors: Al-Sulaiman A,Al-Rajeh S,Iyer V

    更新日期:1986-05-01 00:00:00

  • CK-MM autoantibodies: prevalence, immune complexes, and effect on CK clearance.

    abstract::Although the blood level of creatine kinase (CK) is the most commonly used marker of muscle injury, there is marked interindividual variability in this measure. Part of this variability may be attributed to variability in the rate of CK clearance from the circulation. In this study, we assessed the possibility that CK...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20594

    authors: Warren GL,O'farrell L,Rogers KR,Billings KM,Sayers SP,Clarkson PM

    更新日期:2006-09-01 00:00:00

  • Urinary retention and sympathetic sphincter obstruction in axonal Guillain-Barré syndrome.

    abstract::A 62-year-old woman with axonal Guillain-Barré syndrome developed weakness and urinary retention simultaneously. The retention failed to recover for 10 months even after she regained the ability to walk. The patient exhibited no postural hypotension. Videourodynamics showed that the retention was caused not by the bla...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20639

    authors: Sakakibara R,Uchiyama T,Tamura N,Kuwabara S,Asahina M,Hattori T

    更新日期:2007-01-01 00:00:00

  • Effect of spinal cord TRH deficiency on lower motorneuron function in the rat.

    abstract::Thyrotropin-releasing hormone (TRH), present in high concentrations in the mammalian spinal cord, exerts excitatory effects on the alpha-motorneuron (AMN) via axodendritic contacts. We used the neurotoxin 5,7-dihydroxytryptamine (5,7-DHT) to deplete TRH from the ventral horn of the spinal cord of adult rats to determi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880100504

    authors: Van den Bergh P,Kelly JJ Jr,Adelman L,Munsat TL,Jackson IM,Lechan RM

    更新日期:1987-06-01 00:00:00

  • Stretch-induced spinal accessory nerve palsy.

    abstract::Left spinal accessory nerve palsy occurred in a young man when he quickly turned his head to the right while his shoulders were pulled down by heavy hand-held objects. Electrophysiologic studies demonstrated partial axonotmesis of the spinal accessory nerve branches innervating the sternocleidomastoid and upper and mi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880110210

    authors: Logigian EL,McInnes JM,Berger AR,Busis NA,Lehrich JR,Shahani BT

    更新日期:1988-02-01 00:00:00

  • Elucidation of muscle-binding peptides by phage display screening.

    abstract::Muscle makes up the largest tissue volume of the body, yet its size makes muscle-specific therapy difficult. This becomes particularly relevant when approaches to gene therapy for inherited myopathies are evaluated. Thus, a mechanism to target constructs or pharmaceuticals to muscle following intravenous injection wou...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199904)22:4<460::aid-mus6>

    authors: Samoylova TI,Smith BF

    更新日期:1999-04-01 00:00:00

  • Muscle carnitine in hypo- and hyperthyroidism.

    abstract::Weakness is common in both hyper- and hypothyroidism, and skeletal muscle L-carnitine may play a role in this regard, as suggested by studies indicating abnormal levels of carnitine in serum and urine of patients with thyroid dysfunction. Skeletal muscle samples were obtained for carnitine analysis from control subjec...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20336

    authors: Sinclair C,Gilchrist JM,Hennessey JV,Kandula M

    更新日期:2005-09-01 00:00:00

  • Randomized controlled trial of strength training in post-polio patients.

    abstract::Many post-polio patients develop new muscle weakness decades after the initial illness. However, its mechanism and treatment are controversial. The purpose of this study was to test the hypotheses that: (1) after strength training, post-polio patients show strength improvement comparable to that seen in the healthy el...

    journal_title:Muscle & nerve

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1002/mus.10327

    authors: Chan KM,Amirjani N,Sumrain M,Clarke A,Strohschein FJ

    更新日期:2003-03-01 00:00:00

  • Sparing of the flexor carpi ulnaris in ulnar neuropathy at the elbow.

    abstract::A common misconception attributes sparing of the flexor carpi ulnaris (FCU) in ulnar neuropathy at the elbow (UNE) to its innervating branch arising "at or above the elbow." We examined the relationship of FCU branches to the medial epicondyle (ME) and humeroulnar aponeurotic arcade (HUA) in 30 cadaver elbows. In only...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880121203

    authors: Campbell WW,Pridgeon RM,Riaz G,Astruc J,Leahy M,Crostic EG

    更新日期:1989-12-01 00:00:00

  • A large German kindred with cold-aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene.

    abstract::Muscle sodium-channel disorders cover a spectrum of rare myotonic diseases. In a German family with 17 affected individuals in four generations, we identified a heterozygous missense mutation in exon 24 A1481D (c.4442 C>A) of the voltage-gated sodium channel gene (SCN4A) alpha subunit. Phenotypes of 12 family members ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20733

    authors: Schoser BG,Schröder JM,Grimm T,Sternberg D,Kress W

    更新日期:2007-05-01 00:00:00

  • Motor involvement in acute herpes zoster.

    abstract::Motor involvement in acute herpes zoster is considered rare, but its incidence is unknown. In a sample of 40 patients with acute herpes zoster of varying severity, an abnormal electromyogram (EMG) (fibrillation, positive waves, high-frequency discharges) was found in 21 (53%), suggesting extension of inflammation to t...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199711)20:11<1433::aid-mus

    authors: Haanpää M,Häkkinen V,Nurmikko T

    更新日期:1997-11-01 00:00:00

  • Pulmonary function and electromyographic study of respiratory muscles in myotonic dystrophy.

    abstract::Ten adult myotonic dystrophy patients underwent measurements of lung function, maximal dynamic and static ventilatory efforts, and respiratory muscle electromyography (EMG). EMG studies were performed during spontaneous breathing or when subjects breathed through high inspiratory or expiratory resistive loads. Present...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880080708

    authors: Jammes Y,Pouget J,Grimaud C,Serratrice G

    更新日期:1985-09-01 00:00:00

  • Response to exercise of patients with idiopathic hyper-CK-emia.

    abstract::Patients with an idiopathic increase in serum creatine kinase (CK) levels (hyper-CK-emia) have a benign prognosis, but symptoms may be disabling in daily life. Previous studies have suggested that physical exercise increases the severity of complaints in these patients. We studied whether maximal and submaximal bouts ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.10232

    authors: Reijneveld JC,Te Boekhorst BC,Zonderland ML,Kalmijn S,Notermans NC

    更新日期:2002-12-01 00:00:00

  • Acquired neuromyotonia and peripheral neuropathy in a patient with Hodgkin's disease.

    abstract::Acquired neuromyotonia is characterized by hyperexcitability of motor nerves resulting in continuous muscle fiber activity. It occurs most often as a paraneoplastic syndrome in patients with cancers of the immune system. Antibodies against voltage-gated potassium channels (VGKCs) have been detected in some patients. P...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.1078

    authors: Lahrmann H,Albrecht G,Drlicek M,Oberndorfer S,Urbanits S,Wanschitz J,Zifko UA,Grisold W

    更新日期:2001-06-01 00:00:00

  • Comparison of analysis approaches for phase III clinical trials in amyotrophic lateral sclerosis.

    abstract:INTRODUCTION:In this study we explore several methods for incorporating survival information in the analysis of Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS) scores. METHODS:ALSFRS scores and patient survival times were simulated based on estimates from a recent clinical trial. Six analysis approaches...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23392

    authors: Healy BC,Schoenfeld D

    更新日期:2012-10-01 00:00:00

  • Painful cramps and giant myotonic discharges in a family with the Nav1.4-G1306A mutation.

    abstract:INTRODUCTION:Two previously reported Norwegian patients with painful muscle cramps and giant myotonic discharges were genotyped and compared with those of members of 21 families harboring the same mutation. METHODS:Using primers specific for SCN4A and CLCN1, the DNA of the Norwegian family members was amplified and bi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24672

    authors: Torbergsen T,Jurkat-Rott K,Stålberg EV,Løseth S,Hødneø A,Lehmann-Horn F

    更新日期:2015-10-01 00:00:00

  • Midbrain vs. pontine medial longitudinal fasciculus lesions: the utilization of masseter and blink reflexes.

    abstract::Masseter (MR) and blink reflexes (BL) were investigated in 51 patients with internuclear ophthalmoplegia (INO) due to multiple sclerosis (28) and lacunar infarction (23). The MR was abnormal in 20 of 23 cases with bilateral INO and in 21 of 28 with unilateral INO. The R1 component of the BL (BL-R1) was abnormal in 7 o...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880140406

    authors: Hopf HC,Thömke F,Gutmann L

    更新日期:1991-04-01 00:00:00

  • Adipose stem cells enhance myoblast proliferation via acetylcholine and extracellular signal-regulated kinase 1/2 signaling.

    abstract:INTRODUCTION:In this study we investigated the interaction between adipose tissue-derived stem cells (ASCs) and myoblasts in co-culture experiments. METHODS:Specific inductive media were used to differentiate ASCs in vitro into a Schwann cell-like phenotype (differentiated adipose tissue-derived stem cells, or dASCs) ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25741

    authors: El-Habta R,Kingham PJ,Backman LJ

    更新日期:2018-02-01 00:00:00

  • VCP myopathy: A family with unusual clinical manifestations.

    abstract:INTRODUCTION:Valosin-containing protein (VCP) variants that affect muscle, bone, and the nervous system are termed multisystem proteinopathy. VCP myopathy is manifested as limb-girdle weakness, distal weakness and scapuloperoneal weakness. METHODS:We reviewed clinical, genetic, and muscle biopsy data from 6 members of...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26389

    authors: Guo X,Zhao Z,Shen H,Qi B,Li N,Hu J

    更新日期:2019-03-01 00:00:00

  • Pseudometabolic presentation of dystrophinopathy due to a missense mutation.

    abstract::Exercise intolerance with myalgia, muscle stiffness, and recurrent rhabdomyolysis due to mutations in the DMD gene can mimic metabolic myopathies leading to delayed or inaccurate diagnoses. In this retrospective chart review, we report 3 unrelated boys with exertional myalgia, muscle stiffness, myoglobinuria, and norm...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21823

    authors: Veerapandiyan A,Shashi V,Jiang YH,Gallentine WB,Schoch K,Smith EC

    更新日期:2010-12-01 00:00:00

  • Single motor unit H-reflex in motor neuron disorders.

    abstract::The latency fluctuation of single motor unit potentials (MUPH) in the H-reflex is greater than the latency fluctuation of MUPs in the direct (MUPM) and recurrent (MUPF) responses. This has been attributed to the variability in the impulse generation at the site of nerve stimulation, and to the variation in the synapti...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880150604

    authors: Soliven B,Maselli RA

    更新日期:1992-06-01 00:00:00

  • Limits of normal nerve function during high-frequency stimulation.

    abstract::We studied the effects of prolonged high-frequency stimulation in normal rat tail nerves. Nerves could conduct impulses at 50 Hz for 5 hours without complete conduction block. However, over time there was a significant decrease in amplitude and increase in latency of the compound nerve action potential (CNAP), which g...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880130402

    authors: Robinson LR,Nielsen VK

    更新日期:1990-04-01 00:00:00

  • Diagnostic yield of stimulation and voluntary single-fiber electromyography in myasthenia gravis.

    abstract::Voluntary and stimulation single-fiber electromyography were performed in the extensor digitorum communis muscle of 15 myasthenic patients. The increase in mean and individual mean consecutive difference as well as the proportion of blocking in the volitional activation were greater than in the stimulation method. The...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199808)21:8<1081::aid-mus1

    authors: Murga L,Sánchez F,Menéndez C,Castilla JM

    更新日期:1998-08-01 00:00:00

  • Maximal isometric muscle strength values obtained By hand-held dynamometry in children between 6 and 15 years of age.

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    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25180

    authors: Escobar RG,Munoz KT,Dominguez A,Banados P,Bravo MJ

    更新日期:2017-01-01 00:00:00

  • Effects of extracorporeal shock-wave lithotripsy directed at the parotid gland on oxidative stress parameters and some trace element levels in facial nerve of rats.

    abstract:INTRODUCTION:This study was designed to assess the effect of extracorporeal shock-wave lithotripsy (ESWL) exposure of the parotid gland on oxidative stress and some trace element levels in the facial nerves of rats. METHODS:Twelve male Wistar albino rats were divided into two groups, each consisting of 6 animals. The ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.22326

    authors: Kavak S,Garca MF,Gecit I,Meral I,Cengiz N,Demir H

    更新日期:2012-04-01 00:00:00

  • Late motor involvement in cases presenting as "chronic sensory demyelinating polyneuropathy".

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    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880180411

    authors: Berger AR,Herskovitz S,Kaplan J

    更新日期:1995-04-01 00:00:00

  • Electromyographic and lower extremity short time to inversion recovery magnetic resonance imaging findings in lumbar radiculopathy.

    abstract::To determine if short TI (time to inversion) recovery (STIR) magnetic resonance imaging (MRI) is useful in assessing lower extremity (LE) denervation in subacute lumbar radiculopathy (LR), 25 subjects underwent lumbar spine MRI, LE STIR MRI and needle electromyography (EMG). In 23 (92%) subjects there was a positive c...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199709)20:9<1191::aid-mus1

    authors: Carter GT,Fritz RC

    更新日期:1997-09-01 00:00:00