Paulus W, Peiffer J, Becker I, Roggendorf W, Schumm F
Institut für Hirnforschung, Eberhard-Karls-Universität, Tübingen, Federal Republic of Germany.
J Neurol. 1988 Jul;235(6):343-7. doi: 10.1007/BF00314229.
The third case of adult-onset rod disease (nemaline myopathy) with abundant myofibrillar as well as intranuclear rods is described. The 61-year-old woman suffered from progressive weakness of proximal extremities and of the neck, mimicking polymyositis. Muscle biopsy revealed a striking myopathic pattern, with intranuclear rods occurring in 31% of the fibres. On light and electron microscopy and by immunohistochemical study, the rods differed from myofibrillar rods. The absence of alpha-actinin in intranuclear rods suggests an enhanced readiness of actin filaments to bind to diverse proteins, instead of overproduction of alpha-actinin as the pathogenetic basis of the rod formation.