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Spinal cord sarcoidosis: report of seven cases
Authors:L Varron  C Broussolle  J-P Candessanche  R Marignier  H Rousset  J Ninet  P Sève
Institution:Hospices Civils de Lyon, Universitéde Lyon 1, Lyon, France;;and Centre Hospitalier Universitaire de Saint Etienne, UniversitéJean Monnet, Saint-Étienne, France
Abstract:Background:  Spinal cord involvement in sarcoidosis is rare, occurring in <1% of patients with sarcoidosis.
Methods:  We report seven cases of spinal cord sarcoidosis, seen in two French hospitals over a 13-year period. Presentation of disease, methods of diagnosis and response to treatment, with quantification according to the reduction of the modified Rankin scale (MRS), were noted.
Results:  Six patients presented insidious paresthesias or weakness and one a sudden paraplegia. Average MRS at diagnosis was to 2. Spine MRI showed one or several intramedullary lesions in all cases. Diagnosis was confirmed by extra-neural tissue biopsies in all cases, including mediastinoscopy (two patients), coelioscopy (one patient), bronchoscopy (one patient), salivary gland biopsy (one patient) and skin biopsy (two patients). The average follow-up for the group was 49.4 months. All patients responded to corticosteroid therapy with a median reduction of MRS of one point. Five patients received immunosuppressive therapy: cyclophosphamide (two patients), methotrexate (two patients), azathioprine (one patient), mycophenolate mofetyl (one patient), with an inconstant benefit. Patients who received cyclophosphamide presented severe fungaemia.
Conclusion:  Based on our study and literature analysis, we propose an algorithm for treatment of spinal cord sarcoidosis.
Keywords:immunosuppression  neurosarcoidosis  spinal disease
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