Longitudinally extensive transverse myelitis in systemic lupus erythematosus: Case report and review of the literature

التفاصيل البيبلوغرافية
العنوان: Longitudinally extensive transverse myelitis in systemic lupus erythematosus: Case report and review of the literature
المؤلفون: Ryan T. Fitzgerald, Ariel Bailey, Raffaele Nardone, Giulio Zuccoli
المصدر: Clinical Neurology and Neurosurgery. 129:57-61
بيانات النشر: Elsevier BV, 2015.
سنة النشر: 2015
مصطلحات موضوعية: Adult, medicine.medical_specialty, Poor prognosis, Pathology, Myelitis, Myelitis, Transverse, Transverse myelitis, immune system diseases, Epidemiology, medicine, Humans, Lupus Erythematosus, Systemic, In patient, skin and connective tissue diseases, Autoantibodies, Aquaporin 4, Neuromyelitis optica, medicine.diagnostic_test, business.industry, Neuromyelitis Optica, Magnetic resonance imaging, General Medicine, Prognosis, Spinal cord, medicine.disease, Magnetic Resonance Imaging, Dermatology, medicine.anatomical_structure, Spinal Cord, Female, Surgery, Neurology (clinical), business
الوصف: Objective To report a case of longitudinally extensive transverse myelitis (LETM), a rare but disabling condition defined as a lesion of the spinal cord that extends over four or more vertebrae on MRI, in association with systemic lupus erythematosus (SLE). Methods We present a rare case of LETM involving the cervical and thoracic spinal cord in a patient with SLE and review the existing literature on the association of lupus-associated myelitis. Results LETM is included within the diagnostic criteria for Neuromyelitis Optica (NMO), but is also known to be associated with a wide range of auto-immune diseases. Only 37 cases of LETM in patients with SLE have been previously described. We performed an updated review on epidemiology, pathophysiology, clinical features, diagnosis, management, and prognosis of LETM in the setting of SLE. Conclusion Due to the generally poor prognosis of LETM in SLE patients, prompt diagnosis and treatment is of critical importance for a positive clinical outcome. We provide a comprehensive perspective of past and current literature in order to aid diagnosis and management of this rare phenomenon.
تدمد: 0303-8467
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07a98b0c3b1fba60d88139eb5c1cff42Test
https://doi.org/10.1016/j.clineuro.2014.11.014Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....07a98b0c3b1fba60d88139eb5c1cff42
قاعدة البيانات: OpenAIRE