장딴지신경 조직검사에서 재수초화 신경섬유가 현저하게 증가한 케네디병
Kennedy Disease Showing Prominent Remyelinating Features of Sural Nerve
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We report a 55-year-old man with chronic weakness of both legs with recently experienced nasal voice. Despite the absence of sensory symptoms, electrophysiologic studies revealed the presence of sensorimotor polyneuropathy. A sural-nerve biopsy showed remarkable reduction of large myelinated fibers with prominent remyelination. Intravenous immunoglobulin was administered due to suspected chronic demyelinating neuropathy, but had no effect. Abnormal trinucleotide-repeat expansion of the androgen receptor gene was subsequently detected in both the patient and his family. These observation indicate that prominent remyelinating features are not necessarily indicative of demyelinating neuropathy.
Abstract
We report a 55-year-old man with chronic weakness of both legs with recently experienced nasal voice. Despite the absence of sensory symptoms, electrophysiologic studies revealed the presence of sensorimotor polyneuropathy. A sural-nerve biopsy showed remarkable reduction of large myelinated fibers with prominent remyelination. Intravenous immunoglobulin was administered due to suspected chronic demyelinating neuropathy, but had no effect. Abnormal trinucleotide-repeat expansion of the androgen receptor gene was subsequently detected in both the patient and his family. These observation indicate that prominent remyelinating features are not necessarily indicative of demyelinating neuropathy.
참고문헌 (10)
- Dyck PJ, "Permanent axotomy, a model of axonal atrophy and secondary segmental demyelination and remyelination", Ann Neurol, 9, pp.575~583 (1981)
- Adachi H, "Pathogenesis and molecular targeted therapy of spinal and bulbar muscular atrophy", Neuropathol Appl Neurobiol, 33, pp.135~151 (2007)
- Terao S, "The lateral corticospinal tract and spinal ventral horn in X-linked recessive spinal and bulbar muscular atrophy: a quantitative study", Acta Neuropathol, 93, pp.1~6 (1997)
- Li M, "Primary sensory neurons in X-linked recessive bulbospinal neuropathy: histopathology and androgen receptor gene expression", Muscle Nerve, 18, pp.301~308 (1995)
- Li M, "Nuclear inclusions of the androgen receptor protein in spinal and bulbar muscular atrophy", Ann Neurol, 44, pp.249~254 (1998)
- La Spada AR, "Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy", Nature, 352, pp.77~79 (1991)
- Soraru G, "Spinal and bulbar muscular atrophy: skeletal muscle pathology in male patients and heterozygous females", J Neurol Sci, 264, pp.100~105 (2008)
- Doyu M, "Androgen receptor mRNA with increased size of tandem CAG repeat is widely expressed in the neural and nonneural tissues of X-linked recessive bulbospinal neuronopathy", J Neurol Sci, 127, pp.43~47 (1994)
- Sobue G, "X-linked recessive bulbospinal neuronopathy. A clinicopathological study", Brain, 112, pp.209~232 (1989)
- Saito T, "A case of X-linked recessive bulbospinal muscular atrophy with demyelinating neuropathy and hypertrophy of the calves", Rinsho Shinkeigaku, 33, pp.514~518 (1993)
