𝔖 Bobbio Scriptorium
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Transverse myelitis in mixed connective tissue disease

✍ Scribed by Terry D. Weiss; James S. Nelson; Robert M. Woolsey; Jack Zuckner; Andrew R. Baldassare


Publisher
John Wiley and Sons
Year
1978
Tongue
English
Weight
970 KB
Volume
21
Category
Article
ISSN
0004-3591

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✦ Synopsis


Abstract

Neurologic disease is reported to occur in just 10% of patients with mixed connective tissue disease (MCTD). Most commonly, this is manifested by mild trigeminal neuralgia. This report details the clinical and neuropathologic findings of transverse myelitis in a patient with MCTD. Neurologic features include progressive areflexic paraplegia with loss of bowel and bladder function. Neuropathologically there was thinning of the thoracic cord, widespread loss of axons and myelin sheaths, reactive astrocytosis, macrophage formation, vascular thickening with perivascular chronic inflammatory cell infiltration, and calcium deposits. This case demonstrates that severe neurologic disease unresponsive to therapy can occur in MCTD.


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alleles may actually operate against its formation. Alternatively, it is possible that immune response genes which promote antibodies to nRNP may not be represented on DRZlMBl/MTl and DR3/MT2 bearing haplotypes. Thus, the presence of both sets of alleles, as seen in our patients, might exclude this