Amphiphysin-positive paraneoplastic myelitis and stiff-person syndrome
نویسندگان
چکیده
Finding the underlying etiology of transverse myelitis (TM) can be challenging, as several disorders, including multiple sclerosis (MS), neuromyelitis optica, acute disseminated encephalomyelitis, postvaccine myelitis, Sjögren disease, neurosarcoidosis, infectious myelopathies, or idiopathic TM, may be causative. Paraneoplastic myelopathy, another differential diagnosis, is associated with a broad range of neoplasms and bears a severe risk to develop disability. Stiffperson syndrome (SPS) can occur as a result of some neoplasms and is characterized by skeletal muscle rigidity and spasms. We present the case of a patient with suspected MS who eventually was diagnosed with paraneoplastic TM and SPS, both associated with antibodies to amphiphysin.
منابع مشابه
Stiff leg syndrome and myelitis with anti-amphiphysin antibodies: a common physiopathology?
culty in walking. The symptoms had first appeared 2 weeks earlier. Her medical history included type 2 diabetes treated with metformin and a thyroid goiter treated with surgery and levothyroxine. On clinical examination, she presented permanent hypertonia in the lower limb and bilateral dystonia of the extensor hallucis longus muscles. Intermittent spasms were associated with hypertonia. The sp...
متن کاملStiff-person syndrome with amphiphysin antibodies: distinctive features of a rare disease.
BACKGROUND Stiff-person syndrome (SPS), formerly Stiff-man syndrome, is a rare autoimmune disease usually exhibiting severe spasms and thoracolumbar stiffness, with very elevated glutamic acid decarboxylase antibodies (GAD Ab). A paraneoplastic variant, less well characterized, is associated with amphiphysin antibodies (amphiphysin Ab). The objective of this study was to identify distinctive cl...
متن کامل[Stiff-person syndrome and other myelopathies constitute paraneoplastic neurological syndromes].
Stiff-person syndrome (SPS) is an autoimmune neurological disorder characterized by rigidity of the trunk and proximal limb muscles, intermittent superimposed spasms, and increased sensitivity to external stimuli. It has been more than 50 years since Moerch and Woltman reported the first 14 cases with this syndrome. During the last half century, many autoantibodies discovered, such as anti-glut...
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Stiff-person syndrome is a rare neurological disorder characterized by stiffness of skeletal muscles with superimposed spasms. The syndrome is a putative autoimmune disease occurring as an idiopathic or paraneoplastic condition. It is often associated with antibodies to glutamic acid decarboxylase (GAD) or, less commonly, to the 128 kD synaptic protein later amphiphysin (AMPH) and few other aut...
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Colaço MN, Toyka KV, Sommer C, et al. Human Stiff person syndrome IgGcontaining high-titer anti-GAD65 autoantibodies induce motor dysfunction in rats. Exp Neurol 2013; 239: 202–9. Irani SR, Gelfand JM, Al-Diwani A, Vincent A. Cell-surface central nervous system autoantibodies: Clinical relevance and emerging paradigms. Ann Neurol 2014; 76: 168–84. Lancaster E, Lai M, Peng X, Hughes E, Constanti...
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