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Amyotrophic Lateral Sclerosis and Multiple Sclerosis Overlap: A Case Report
Author(s) -
Francesca Trojsi,
Anna Sagnelli,
Giovanni Cirillo,
Giovanni Piccirillo,
Cinzia Femiano,
Francesco Izzo,
Maria Rosaria Monsurrò,
Gioacchino Tedeschi
Publication year - 2012
Publication title -
case reports in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.2
H-Index - 20
eISSN - 1687-9627
pISSN - 1687-9635
DOI - 10.1155/2012/324685
Subject(s) - amyotrophic lateral sclerosis , medicine , multiple sclerosis , fluid attenuated inversion recovery , magnetic resonance imaging , pathology , pathological , progressive muscular atrophy , atrophy , upper motor neuron , cerebrospinal fluid , radiology , disease , immunology
The concurrence of amyotrophic lateral sclerosis (ALS) and multiple sclerosis (MS) is extremely rare. We reported the case of a 33-year-old woman with a past history of paresthesias at the right hand, who developed progressive quadriparesis with muscular atrophy of limbs and, finally, bulbar signs and dyspnea. Clinical and neurophysiologic investigations revealed upper and lower motor neuron signs in the bulbar region and extremities, suggesting the diagnosis of ALS. Moreover, magnetic resonance imaging (MRI) and cerebrospinal fluid (CSF) analysis demonstrated 3 periventricular and juxtacortical lesions, hyperintense in T2 and FLAIR sequences, and 3 liquoral immunoglobulin G (IgG) oligoclonal bands, consistent with diagnosis of primary progressive MS (PPMS). This unusual overlap of ALS and MS leads to the discussion of a hypothetical common pathological process of immunological dysfunction in these two disorders, although the role of immune response in ALS remains ambivalent and unclear.

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