Ataxic sensory neuronopathy in a patient with systemic lupus erythematosus.

Abstract:

:The occurrence of ataxic sensory neuronopathy (ASN) is rare in patients with connective tissue diseases (CTDs). ASN has been described in case reports and case series in patients with CTDs, mostly Sjögren's syndrome, and most often occurring during middle or old age. ASN in association with systemic lupus erythematosus (SLE) is extremely rare; there has been only one reported case in the literature. In addition, to our knowledge, adolescent onset of symptoms in CTD-associated ASN has not been reported previously. We report the case of a young woman who presented with ASN, characterized by sensory ataxia, with elevated antinuclear antibodies, leukopenia and anemia; she fulfilled the diagnostic criteria for SLE about 7 years after the onset of sensory ataxia. Our case points out that ASN may be the initial presenting feature of SLE. SLE should be included in the differential diagnosis of ASN, especially in patients of young age.

journal_name

Lupus

journal_title

Lupus

authors

Wang JC,Lin YC,Yang TF,Lin HY

doi

10.1177/0961203311434105

subject

Has Abstract

pub_date

2012-07-01 00:00:00

pages

905-9

issue

8

eissn

0961-2033

issn

1477-0962

pii

0961203311434105

journal_volume

21

pub_type

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