期刊论文详细信息
BMC Musculoskeletal Disorders
Electrophysiological differences between Hirayama disease, amyotrophic lateral sclerosis and cervical spondylotic amyotrophy
Chao-Jun Zheng1  Li-Xun Wang1  Xin-Lei Xia1  Fei-Zhou Lu1  Jian-Yuan Jiang1  Xiang Jin1 
[1] Department of Orthopedics, Huashan Hospital, Fudan University, Shanghai 200040, China
关键词: Action potential;    Spondylotic amyotrophy;    Amyotrophic lateral aclerosis;    Electrophysiological differentiation;    Hirayama disease;   
Others  :  1118643
DOI  :  10.1186/1471-2474-15-349
 received in 2014-07-07, accepted in 2014-10-08,  发布年份 2014
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【 摘 要 】

Background

Hirayama disease (HD), amyotrophic lateral sclerosis (ALS) or cervical spondylotic amyotrophy (CSA) may result in atrophy of intrinsic hand and forearm muscles. The incidence of HD is low, and it is rarely encountered in the clinical setting. Consequently, HD is often misdiagnosed as ALS or CSA. It is important to differentiate these diseases because HD is caused by a benign focal lesion that is limited to the upper limbs.

Methods

The thenar and hypothenar compound muscle action potential (CMAP) amplitude of the upper limbs of 100 HD, 97 ALS and 32 CSA cases were reviewed; 35 healthy individuals were included as controls. Seventy-eight percent, 38% and 69% of patients with HD, ALS or CSA had unilateral involvement; the remaining patients were affected bilaterally. Thenar and hypothenar CMAP amplitude evoked by ulnar stimulation was compared with CMAP evoked by median stimulation.

Results

The ulnar/median CMAP ratio was found to be lower in HD (0.55 ± 0.41, P < 0.0001), higher in ALS (2.28 ± 1.15, P < 0.0001) and no different in CSA (1.21 ± 0.53, P > 0.05) compared with the normal range from previous studies (0.89-1.60) and with the healthy controls (1.15 ± 0.23). Conduction velocities of the sensory and motor nerves, the amplitude of the sensory nerve action potential, and the CMAP amplitude of the unaffected limb were all normal.

Conclusions

The hand muscles were differentially affected between patients with HD, ALS and CSA. The ulnar/median CMAP ratio could be used to distinguish these three diseases.

【 授权许可】

   
2014 Jin et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Hirayama K, Toyokura Y, Tsubaki T: Juvenile muscular atrophy of unilateral upper extremity: a new clinical entity. Psychiatry Neurol Jpn 1959, 61:2190-2198.
  • [2]Tandan R: Disorders of the upper and lower motor neurons. In Neurology in clinical practice. 2nd edition. Boston: utterworth-Heinemann; 1996:1823-1852.
  • [3]Jiang SD, Jiang LS, Dai LY: Cervical spondylotic amyotrophy. Eur Spine J 2011, 20(3):351-357.
  • [4]Crandall PH, Batzdorf U: Cervical spondylotic myelopathy. J Neurosurg 1966, 25(1):57-66.
  • [5]Tsuboi Y, Tokumaru Y, Hirayama K: Clinical difference between "proximal" and "distal" type of cervical spondylotic amyotrophy. Rinsho shinkeigaku =Clin Neurol 1995, 35(2):147-152.
  • [6]Tashiro K, Kikuchi S, Itoyama Y, Tokumaru Y, Sobue G, Mukai E, Akiguchi I, Nakashima K, Kira J, Hirayama K: Nationwide survey of juvenile muscular atrophy of distal upper extremity (Hirayama disease) in Japan. Amyotroph Lateral Scler 2006, 7(1):38-45.
  • [7]Hirayama K, Tsubaki T, Toyokura Y, Okinaka S: Juvenile muscular atrophy of unilateral upper extremity. Neurology 1963, 13:373-380.
  • [8]Singh N, Sachdev KK, Susheela AK: Juvenile muscular atrophy localized to arms. Arch Neurol 1980, 37(5):297-299.
  • [9]Chen CJ, Hsu HL, Tseng YC, Lyu RK, Chen CM, Huang YC, Wang LJ, Wong YC, See LC: Hirayama flexion myelopathy: neutral-position MR imaging findings–importance of loss of attachment. Radiology 2004, 231(1):39-44.
  • [10]Sonwalkar HA, Shah RS, Khan FK, Gupta AK, Bodhey NK, Vottath S, Purkayastha S: Imaging features in Hirayama disease. Neurol India 2008, 56(1):22-26.
  • [11]Brooks BR: El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial "Clinical limits of amyotrophic lateral sclerosis" workshop contributors. J Neurol Sci 1994, 124(Suppl):96-107.
  • [12]Inui Y, Miyamoto H, Sumi M, Uno K: Clinical outcomes and predictive factors relating to prognosis of conservative and surgical treatments for cervical spondylotic amyotrophy. Spine 2011, 36(10):794-799.
  • [13]Kuwabara S, Sonoo M, Komori T, Shimizu T, Hirashima F, Inaba A, Misawa S, Hatanaka Y, Tokyo Metropolitan Neuromuscular Electrodiagnosis Study G: Dissociated small hand muscle atrophy in amyotrophic lateral sclerosis: frequency, extent, and specificity. Muscle Nerve 2008, 37(4):426-430.
  • [14]Lyu RK, Huang YC, Wu YR, Kuo HC, Ro LS, Chen CM, Chang HS: Electrophysiological features of Hirayama disease. Muscle Nerve 2011, 44(2):185-190.
  • [15]Hirayama K: Juvenile muscular atrophy of distal upper extremity (Hirayama disease). Intern Med 2000, 39(4):283-290.
  • [16]Wilbourn AJ: The "split hand syndrome". Muscle Nerve 2000, 23(1):138.
  • [17]Elsheikh B, Kissel JT, Christoforidis G, Wicklund M, Kehagias DT, Chiocca EA, Mendell JR: Spinal angiography and epidural venography in juvenile muscular atrophy of the distal arm "Hirayama disease". Muscle Nerve 2009, 40(2):206-212.
  • [18]Restuccia D, Rubino M, Valeriani M, Mirabella M, Sabatelli M, Tonali P: Cervical cord dysfunction during neck flexion in Hirayama’s disease. Neurology 2003, 60(12):1980-1983.
  • [19]Toma S, Shiozawa Z: Amyotrophic cervical myelopathy in adolescence. J Neurol Neurosurg Psychiatry 1995, 58(1):56-64.
  • [20]Keegan JJ: The cause of dissociated motor loss in the upper extremity with cervical spondylosis. J Neurosurg 1965, 23(5):528-536.
  • [21]Yanagi T, Kato H, Sobue I: Clinical characteristics of cervical spondylotic amyotrophy. Rinsho shinkeigaku =Clin Neurol 1976, 16:520-528.
  • [22]Katsuoka H, Mimori Y, Harada A, Kitamura T, Kurokawa K, Nakamura S: An elderly case of juvenile muscular atrophy in the unilateral upper extremity with tremor in both hands. Nihon Ronen Igakkai zasshi Japanese J Geriatr 1999, 36(4):279-283.
  • [23]Okumura H, Homma TT: Juvenile compression myelopathy in the cervical spine. Spine 1994, 19(1):72-76.
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