주요 근육병리 소견을 바탕으로 한 근육병의 진단
Diagnostic Approaches to Various Muscle Diseases Based on Muscle Pathology
2
조회
0
다운로드
3
인용
0
참고문헌
키워드
초록
Muscle pathology can give much information to reach the diagnosis of neuromuscular disorders. Major pathological changes occurred in skeletal muscles include muscle fiber atrophy/hypertrophy, necrosis/regeneration, inflammation, myofibrillar disorganization, abnormal inclusions, and disruptions in cellular organelles. Physicians should be able to understand what each of these findings indicates. However, these are not always specific to a certain disease, and instead most of them are commonly found in many of muscle diseases. Thus, muscle pathological findings should be carefully interpreted under the given clinical settings.
Abstract
Muscle pathology can give much information to reach the diagnosis of neuromuscular disorders. Major pathological changes occurred in skeletal muscles include muscle fiber atrophy/hypertrophy, necrosis/regeneration, inflammation, myofibrillar disorganization, abnormal inclusions, and disruptions in cellular organelles. Physicians should be able to understand what each of these findings indicates. However, these are not always specific to a certain disease, and instead most of them are commonly found in many of muscle diseases. Thus, muscle pathological findings should be carefully interpreted under the given clinical settings.
참고문헌 (28)
- Dubowitz V, "Muscle biopsy: a practical approach", pp.2~15 (2013), Elsevier
- 김대성, "근이영양증에서 면역조직화학염색의 진단적 의의", 대한신경과학회지, 24(1), pp.1~13 (2006), 대한신경과학회
- Dubowitz V, "Muscle biopsy: a practical approach", pp.28~54 (2013), Elsevier
- Sewry CA, "Muscle disease: pathology and genetics", pp.19~31 (2013), Wiley-Blackwell
- Dubowitz V, "Muscle biopsy: a practical approach", pp.250~275 (2013), Elsevier
- Park YE, "Characterization of congenital myopathies at a Korean neuromuscular center", Muscle Nerve, 58, pp.235~244 (2018)
- Dubowitz V, "Muscle biopsy: a practical approach", pp.513~538 (2013), Elsevier
- Barresi R, "Muscle disease: pathology and genetics", pp.95~101 (2013), Wiley-Blackwell
- Dubowitz V, "Muscle biopsy: a practical approach", pp.276~301 (2013), Elsevier
- Dubowitz V, "Muscle biopsy: a practical approach", pp.331~344 (2013), Elsevier
- Dubowitz V, "Muscle biopsy: a practical approach", pp.302~330 (2013), Elsevier
- Tanboon J, "Classification of idiopathic inflammatory myopathies:pathology perspectives", Curr Opin Neurol, 32, pp.704~714 (2019)
- Hauerslev S, "Muscle regeneration and inflammation in patients with facioscapulohumeral muscular dystrophy", Acta Neurol Scand, 128, pp.194~201 (2013)
- Mariano A, "Dysferlin-deficient muscular dystrophy and innate immune activation", FEBS J, 280, pp.4165~4176 (2013)
- 박영은, "Clinical and Pathological Features of Korean Patients with DNM2-Related Centronuclear Myopathy", Journal of Clinical Neurology, 10(1), pp.24~31 (2014), 대한신경과학회[DOI]
- Romero NB, "Muscle disease: pathology and genetics", pp.134~144 (2013), Wiley-Blackwell
- Sewry CA, "A rapid immunohistochemical test to distinguish congenital myotonic dystrophy from X-linked myotubular myopathy", Neuromuscul Disord, 22, pp.225~230 (2012)
- Dubowitz V, "Muscle biopsy: a practical approach", pp.446~484 (2013), Elsevier
- 석정임, "클레부딘(clevudine)유발근병증의 임상과 병리특성", 대한신경과학회지, 31(1), pp.26~31 (2013), 대한신경과학회
- Jungbluth H, "Muscle disease:pathology and genetics", pp.214~224 (2013), Wiley-Blackwell
- Lee JM, "Clinical and genetic diversity of nemaline myopathy from a single neuromuscular center in Korea", J Neurol Sci, 383, pp.61~68 (2017)
- Uruha A, "Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance", Curr Opin Neurol, 30, pp.457~463 (2017)
- Park YE, "NEB-related core-rod myopathy with distinct clinical and pathological features", Muscle Nerve, 53, pp.479~484 (2016)
- Selcen D, "Myofibrillar myopathies", Neuromuscul Disord, 21, pp.161~171 (2011)
- 박영은, "Progression of GNE Myopathy Based on the Patient-Reported Outcome", Journal of Clinical Neurology, 15(3), pp.275~284 (2019), 대한신경과학회
- Malerba A, "PABPN1 gene therapy for oculopharyngeal muscular dystrophy", Nat Commun, 8, pp.14848~ (2017)
- Ishiura H, "Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease", Nat Genet, 51, pp.1222~1232 (2019)
- Dubowitz V, "Muscle biopsy: a practical approach", pp.423~435 (2013), Elsevier
