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Z Rheumatol ; 75(9): 939-942, 2016 Nov.
Article in German | MEDLINE | ID: mdl-27581001

ABSTRACT

Spinal epidural lipomatosis (SEL) of the thoracic and lumbar spine is a rare entity, which leads to compression of the spinal canal. The exact pathogenesis is still unknown. It most commonly occurs in patients with long-term exogenous or endogenous glucocorticoid excess or morbid obesity but there are also idiopathic forms. The symptoms depend on the severity of the SEL and can manifest as clinically asymptomatic, non-specific back pain, radiculopathy up to spinal cord compression. The diagnosis is usually achieved by magnetic resonance imaging (MRI) of the affected spinal segments. The treatment varies between discontinuation of glucocorticoids, weight reduction up to multisegmental decompressive laminectomy. The following case report presents the findings of SEL in a patient with steroid-dependent Jo-1 antibody syndrome and provides a current literature review on this rare disease.


Subject(s)
Antibodies, Antinuclear/immunology , Glucocorticoids/adverse effects , Lipomatosis/chemically induced , Lipomatosis/diagnostic imaging , Polymyositis/complications , Spinal Cord Compression/etiology , Diagnosis, Differential , Glucocorticoids/therapeutic use , Humans , Lipomatosis/prevention & control , Magnetic Resonance Imaging/methods , Male , Middle Aged , Polymyositis/diagnosis , Polymyositis/immunology , Spinal Cord Compression/diagnostic imaging , Spinal Cord Compression/prevention & control , Syndrome
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