Related Experiment Video
Updated: Jul 20, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
Transverse myelitis associated with systemic lupus erythematosus (SLE-TM): A review article
Sahil Jain1, Abdulrahman Khormi2, Shirish R Sangle1
1Guy's and St Thomas' Hospitals NHS Trust, London, UK.
Abstract:
Systemic lupus erythematosus-related transverse myelitis (SLE-TM) is a rare but serious complication of SLE, which may result in significant morbidity. Its incidence is estimated between 0.5% and 1% of all SLE patients but may be the presenting feature in 30%-60% of these patients. Unfortunately, due to lack of high-quality studies, data regarding this condition remains limited. Its pathogenesis remains largely unknown and clinical presentation is variable. There are still no set guidelines regarding diagnosis, management, or monitoring and the role of autoantibodies remains controversial. In this review, we aim to summarize the available data regarding the epidemiology, pathogenesis, clinical features, management, and prognosis of this rare disease.
Insights
Systemic lupus erythematosus-related transverse myelitis (SLE-TM) is a rare complication of SLE, impacting 0.5%-1% of patients. This review summarizes current knowledge on SLE-TM epidemiology, pathogenesis, and clinical features due to limited data.
Area of Science:
- Neurology
- Rheumatology
- Immunology
Background:
- Systemic lupus erythematosus-related transverse myelitis (SLE-TM) is a severe neurological complication of Systemic Lupus Erythematosus (SLE).
- It affects an estimated 0.5% to 1% of SLE patients, potentially presenting as the initial symptom in 30% to 60% of cases.
- Limited high-quality research exists, with unknown pathogenesis, variable clinical presentation, and no established diagnostic or management guidelines.
Purpose of the Study:
- To provide a comprehensive review of the current literature on SLE-TM.
- To summarize existing data on epidemiology, pathogenesis, clinical manifestations, and treatment strategies.
- To highlight the need for further research and standardized guidelines for this rare condition.
Main Methods:
- Systematic review of existing medical literature.
- Analysis of epidemiological data, clinical case reports, and observational studies.
- Synthesis of information on pathogenesis, diagnostic criteria, therapeutic interventions, and patient outcomes.
Main Results:
- SLE-TM is a rare but debilitating condition associated with significant patient morbidity.
- The exact pathogenesis remains largely unelucidated, and clinical presentations are diverse.
- Current management strategies lack standardization, and the role of autoantibodies is debated.
Conclusions:
- Further high-quality research is crucial to understand SLE-TM better.
- Development of clear diagnostic, management, and monitoring guidelines is urgently needed.
- Clarifying the role of autoantibodies may improve diagnostic accuracy and therapeutic approaches for SLE-TM.
Related Concept Videos
Graves' Disease I: Introduction
Multiple Sclerosis l: Introduction

