Neurological Disorders

Late-Onset Myopathy Responsive to Immunomodulatory Treatment

Abstract

Menachem Sadeh1*, Yakov Fellig2 and Ron Dabby1

Late-Onset Sporadic Nemaline Myopathy (SLONM) is a rare, treatable or potentially life-threatening, muscle disorder that typically manifests late in life and is characterized by the presence of nemaline rods within muscle fibers, serving as the hallmark of the disease and the key to diagnosis. We report a case of an elderly patient with sub-acute onset of severe weakness affecting the upper and lower limbs, neck extensors and abdominal muscles. Muscle biopsies showed nonspecific myopathic changes without inflammation, and electron microscopy did not reveal rods or aggregates. The laboratory workup was unremarkable except for the detection of Monoclonal Gammopathy of Undetermined Significance (MGUS). Steroid treatment was ineffective; however, there was a notable positive response to intravenous immunoglobulins. The neurological findings, subacute course, normal CK levels, presence of MGUS, and responsiveness to immunoglobulin treatment but not to steroids align with the characteristics of SLONM. We propose that the diagnosis of SLONM should be considered even in the absence of nemaline rods in muscle biopsy, and this should not impede the consideration of immunomodulatory treatment. Future progress in understanding the pathogenetic basis of SLONM may reduce reliance on pathological findings in muscle biopsies for establishing the diagnosis.