Literature DB >> 8295193

Recurrent reflex sympathetic dystrophy as a manifestation of systemic lupus erythematosus.

B E Ostrov1, A H Eichenfield, D P Goldsmith, H R Schumacher.   

Abstract

Reflex sympathetic dystrophy (RSDS) is a syndrome of hyperesthesia and vasomotor disturbance of an extremity, often following trauma or an inflammatory process. We describe a patient with systemic lupus erythematosus (SLE) and recurrent RSDS involving all 4 extremities at various times during her illness. Treatments, including corticosteroid use, physical therapy and at times sympathetic nerve blockade led to the resolution of each episode. We suggest the diagnosis of RSDS be considered in patients with connective tissue diseases who present with atypical pain syndromes not attributable to their primary illness.

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Year:  1993        PMID: 8295193

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   4.666


  1 in total

1.  The prevalence of autoantibodies in complex regional pain syndrome type I.

Authors:  Maaike Dirckx; Marco W J Schreurs; Marissa de Mos; Dirk L Stronks; Frank J P M Huygen
Journal:  Mediators Inflamm       Date:  2015-02-08       Impact factor: 4.711

  1 in total

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