Skip to main content
Top
Published in: Journal of Neurology 10/2013

01-10-2013 | Original Communication

Ultrasonographic nerve enlargement of the median and ulnar nerves and the cervical nerve roots in patients with demyelinating Charcot–Marie–Tooth disease: distinction from patients with chronic inflammatory demyelinating polyneuropathy

Authors: Takamichi Sugimoto, Kazuhide Ochi, Naohisa Hosomi, Tetsuya Takahashi, Hiroki Ueno, Takeshi Nakamura, Yoshito Nagano, Hirofumi Maruyama, Tatsuo Kohriyama, Masayasu Matsumoto

Published in: Journal of Neurology | Issue 10/2013

Login to get access

Abstract

Demyelinating Charcot–Marie–Tooth disease (CMT) and chronic inflammatory demyelinating polyneuropathy (CIDP) are both demyelinating polyneuropathies. The differences in nerve enlargement degree and pattern at multiple evaluation sites/levels are not well known. We investigated the differences in nerve enlargement degree and the distribution pattern of nerve enlargement in patients with demyelinating CMT and CIDP, and verified the appropriate combination of sites/levels to differentiate between these diseases. Ten patients (aged 23–84 years, three females) with demyelinating CMT and 16 patients (aged 30–85 years, five females) with CIDP were evaluated in this study. The nerve sizes were measured at 24 predetermined sites/levels from the median and ulnar nerves and the cervical nerve roots (CNR) using ultrasonography. The evaluation sites/levels were classified into three regions: distal, intermediate and cervical. The number of sites/levels that exhibited nerve enlargement (enlargement site number, ESN) in each region was determined from the 24 sites/levels and from the selected eight screening sites/levels, respectively. The cross-sectional areas of the peripheral nerves were markedly larger at all evaluation sites in patients with demyelinating CMT than in patients with CIDP (p < 0.01). However, the nerve sizes of CNR were not significantly different between patients with either disease. When we evaluated ESN of four selected sites for screening from the intermediate region, the sensitivity and specificity to distinguish between demyelinating CMT and CIDP were 0.90 and 0.94, respectively, with the cut-off value set at four. Nerve ultrasonography is useful to detect nerve enlargement and can clarify morphological differences in nerves between patients with demyelinating CMT and CIDP.
Literature
1.
go back to reference Pareyson D, Marchesi C (2009) Diagnosis, natural history, and management of Charcot–Marie–Tooth disease. Lancet Neurol 8:654–667PubMedCrossRef Pareyson D, Marchesi C (2009) Diagnosis, natural history, and management of Charcot–Marie–Tooth disease. Lancet Neurol 8:654–667PubMedCrossRef
2.
go back to reference England JD, Gronseth GS, Franklin G et al (2009) Practice parameter: evaluation of distal symmetric polyneuropathy: role of laboratory and genetic testing (an evidence-based review). Report of the American Academy of Neurology, American Association of Neuromuscular and Electrodiagnostic Medicine, and American Academy of Physical Medicine and Rehabilitation. Neurology 72:185–192PubMedCrossRef England JD, Gronseth GS, Franklin G et al (2009) Practice parameter: evaluation of distal symmetric polyneuropathy: role of laboratory and genetic testing (an evidence-based review). Report of the American Academy of Neurology, American Association of Neuromuscular and Electrodiagnostic Medicine, and American Academy of Physical Medicine and Rehabilitation. Neurology 72:185–192PubMedCrossRef
3.
go back to reference Ginsberg L, Malik O, Kenton AR et al (2004) Coexistent hereditary and inflammatory neuropathy. Brain 127:193–202PubMedCrossRef Ginsberg L, Malik O, Kenton AR et al (2004) Coexistent hereditary and inflammatory neuropathy. Brain 127:193–202PubMedCrossRef
4.
go back to reference Latov N (2011) Biomarkers of CIDP in patients with diabetes or CMT1. J Peripher Nerv Syst 16:14–17PubMedCrossRef Latov N (2011) Biomarkers of CIDP in patients with diabetes or CMT1. J Peripher Nerv Syst 16:14–17PubMedCrossRef
5.
go back to reference Abe A, Numakura C, Kijima K et al (2011) Molecular diagnosis and clinical onset of Charcot–Marie–Tooth disease in Japan. J Hum Genet 56:364–368PubMedCrossRef Abe A, Numakura C, Kijima K et al (2011) Molecular diagnosis and clinical onset of Charcot–Marie–Tooth disease in Japan. J Hum Genet 56:364–368PubMedCrossRef
6.
go back to reference Schady W, Goulding PJ, Lecky BR et al (1996) Massive nerve root enlargement in chronic inflammatory demyelinating polyneuropathy. J Neurol Neurosurg Psychiatry 61:636–640PubMedCrossRef Schady W, Goulding PJ, Lecky BR et al (1996) Massive nerve root enlargement in chronic inflammatory demyelinating polyneuropathy. J Neurol Neurosurg Psychiatry 61:636–640PubMedCrossRef
7.
go back to reference Duggins AJ, McLeod JG, Pollard JD et al (1999) Spinal root and plexus hypertrophy in chronic inflammatory demyelinating polyneuropathy. Brain 122:1383–1390PubMedCrossRef Duggins AJ, McLeod JG, Pollard JD et al (1999) Spinal root and plexus hypertrophy in chronic inflammatory demyelinating polyneuropathy. Brain 122:1383–1390PubMedCrossRef
8.
go back to reference Midroni G, de Tilly LN, Gray B et al (1999) MRI of the cauda equina in CIDP: clinical correlations. J Neurol Sci 170:36–44PubMedCrossRef Midroni G, de Tilly LN, Gray B et al (1999) MRI of the cauda equina in CIDP: clinical correlations. J Neurol Sci 170:36–44PubMedCrossRef
9.
go back to reference Cellerini M, Salti S, Desideri V et al (2000) MR imaging of the cauda equina in hereditary motor sensory neuropathies: correlations with sural nerve biopsy. AJNR Am J Neuroradiol 21:1793–1798PubMed Cellerini M, Salti S, Desideri V et al (2000) MR imaging of the cauda equina in hereditary motor sensory neuropathies: correlations with sural nerve biopsy. AJNR Am J Neuroradiol 21:1793–1798PubMed
10.
go back to reference Tazawa K, Matsuda M, Yoshida T et al (2008) Spinal nerve root hypertrophy on MRI: clinical significance in the diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy. Intern Med 47:2019–2024PubMedCrossRef Tazawa K, Matsuda M, Yoshida T et al (2008) Spinal nerve root hypertrophy on MRI: clinical significance in the diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy. Intern Med 47:2019–2024PubMedCrossRef
11.
go back to reference Adachi Y, Sato N, Okamoto T et al (2011) Brachial and lumbar plexuses in chronic inflammatory demyelinating polyradiculoneuropathy: MRI assessment including apparent diffusion coefficient. Neuroradiology 53:3–11PubMedCrossRef Adachi Y, Sato N, Okamoto T et al (2011) Brachial and lumbar plexuses in chronic inflammatory demyelinating polyradiculoneuropathy: MRI assessment including apparent diffusion coefficient. Neuroradiology 53:3–11PubMedCrossRef
12.
go back to reference Sinclair CD, Miranda MA, Cowley P et al (2011) MRI shows increased sciatic nerve cross sectional area in inherited and inflammatory neuropathies. J Neurol Neurosurg Psychiatry 82:1283–1286PubMedCrossRef Sinclair CD, Miranda MA, Cowley P et al (2011) MRI shows increased sciatic nerve cross sectional area in inherited and inflammatory neuropathies. J Neurol Neurosurg Psychiatry 82:1283–1286PubMedCrossRef
13.
go back to reference Martinoli C, Schenone A, Bianchi S et al (2002) Sonography of the median nerve in Charcot–Marie–Tooth disease. AJR Am J Roentgenol 178:1553–1556PubMedCrossRef Martinoli C, Schenone A, Bianchi S et al (2002) Sonography of the median nerve in Charcot–Marie–Tooth disease. AJR Am J Roentgenol 178:1553–1556PubMedCrossRef
14.
go back to reference Matsuoka N, Kohriyama T, Ochi K et al (2004) Detection of cervical nerve root hypertrophy by ultrasonography in chronic inflammatory demyelinating polyradiculoneuropathy. J Neurol Sci 219:15–21PubMedCrossRef Matsuoka N, Kohriyama T, Ochi K et al (2004) Detection of cervical nerve root hypertrophy by ultrasonography in chronic inflammatory demyelinating polyradiculoneuropathy. J Neurol Sci 219:15–21PubMedCrossRef
15.
go back to reference Cartwright MS, Brown ME, Eulitt P et al (2009) Diagnostic nerve ultrasound in Charcot–Marie–Tooth disease type 1B. Muscle Nerve 40:98–102PubMedCrossRef Cartwright MS, Brown ME, Eulitt P et al (2009) Diagnostic nerve ultrasound in Charcot–Marie–Tooth disease type 1B. Muscle Nerve 40:98–102PubMedCrossRef
16.
go back to reference Zaidman CM, Al-Lozi M, Pestronk A (2009) Peripheral nerve size in normals and patients with polyneuropathy: an ultrasound study. Muscle Nerve 40:960–966PubMedCrossRef Zaidman CM, Al-Lozi M, Pestronk A (2009) Peripheral nerve size in normals and patients with polyneuropathy: an ultrasound study. Muscle Nerve 40:960–966PubMedCrossRef
17.
go back to reference Van den Bergh PY, Hadden RD, Bouche P et al (2010) European Federation of Neurological Societies; Peripheral Nerve Society. European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society—first revision. Eur J Neurol 17:356–363PubMedCrossRef Van den Bergh PY, Hadden RD, Bouche P et al (2010) European Federation of Neurological Societies; Peripheral Nerve Society. European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society—first revision. Eur J Neurol 17:356–363PubMedCrossRef
18.
go back to reference Hughes RA, Newsom-Davis JM, Perkin GD et al (1978) Controlled trial prednisolone in acute polyneuropathy. Lancet 2:750–753PubMedCrossRef Hughes RA, Newsom-Davis JM, Perkin GD et al (1978) Controlled trial prednisolone in acute polyneuropathy. Lancet 2:750–753PubMedCrossRef
20.
go back to reference Lewis RA, Sumner AJ (1982) The electrodiagnostic distinctions between chronic familial and acquired demyelinative neuropathies. Neurology 32:592–596PubMedCrossRef Lewis RA, Sumner AJ (1982) The electrodiagnostic distinctions between chronic familial and acquired demyelinative neuropathies. Neurology 32:592–596PubMedCrossRef
21.
go back to reference Krajewski KM, Lewis RA, Fuerst DR et al (2000) Neurological dysfunction and axonal degeneration in Charcot–Marie–Tooth disease type 1A. Brain 123:1516–1527PubMedCrossRef Krajewski KM, Lewis RA, Fuerst DR et al (2000) Neurological dysfunction and axonal degeneration in Charcot–Marie–Tooth disease type 1A. Brain 123:1516–1527PubMedCrossRef
22.
go back to reference Lewis RA, Sumner AJ (1999) Electrophysiologic features of inherited demyelinating neuropathies: a reappraisal. Ann N Y Acad Sci 883:321–335PubMedCrossRef Lewis RA, Sumner AJ (1999) Electrophysiologic features of inherited demyelinating neuropathies: a reappraisal. Ann N Y Acad Sci 883:321–335PubMedCrossRef
Metadata
Title
Ultrasonographic nerve enlargement of the median and ulnar nerves and the cervical nerve roots in patients with demyelinating Charcot–Marie–Tooth disease: distinction from patients with chronic inflammatory demyelinating polyneuropathy
Authors
Takamichi Sugimoto
Kazuhide Ochi
Naohisa Hosomi
Tetsuya Takahashi
Hiroki Ueno
Takeshi Nakamura
Yoshito Nagano
Hirofumi Maruyama
Tatsuo Kohriyama
Masayasu Matsumoto
Publication date
01-10-2013
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 10/2013
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-013-7021-0

Other articles of this Issue 10/2013

Journal of Neurology 10/2013 Go to the issue