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Acute Flaccid Myelitis: Current Status and Diagnostic Challenges
1Department of Neurology, University of Texas Medical Branch, Galveston, TX, USA. sxfang@utmb.edu.
Abstract:
Acute flaccid myelitis (AFM) is a sudden-onset polio-like neuromuscular disability found commonly in young children. There is an increasing incidence of confirmed AFM cases in the USA and other countries in recent years, and in association with nonpolio enterovirus infection. This represents a significant challenge to clinicians and causes significant concern to the general public. Acute flaccid paralysis (AFP) is the long-known limb paralytic syndrome caused by a viral pathogen. AFM is a subset of AFP that is also characterized by a limb paralytic condition, but it has certain distinct features such as lesions in magnetic resonance imaging of the spinal cord gray matter. AFM leads to spinal cord, brainstem, or motor neuron dysfunction. The clinical phenotypes, pathology, and patient presentation of AFM closely mimic AFP. This article provides a concise overview of our current understanding of AFM and the clinical features that distinguish AFM from AFP and similar other neurological infectious and autoimmune diseases or disorders. We also discuss the diagnosis, clinical pathology, possible pathogenetic mechanisms, and currently available therapies.
Insights
Acute flaccid myelitis (AFM) is a polio-like condition affecting children, often linked to enterovirus infections. This overview clarifies AFM
Area of Science:
- Neurology
- Infectious Diseases
- Pediatrics
Background:
- Acute flaccid myelitis (AFM) is a sudden-onset, polio-like neuromuscular disability primarily affecting young children.
- There is a concerning increase in confirmed AFM cases globally, often associated with nonpolio enterovirus infections.
- AFM presents a significant clinical challenge and public health concern due to its increasing incidence.
Purpose of the Study:
- To provide a concise overview of current understanding of Acute Flaccid Myelitis (AFM).
- To delineate the clinical features distinguishing AFM from Acute Flaccid Paralysis (AFP) and other neurological disorders.
- To discuss diagnosis, pathology, pathogenesis, and therapies for AFM.
Main Methods:
- Literature review and synthesis of current research on AFM.
- Comparative analysis of clinical phenotypes, pathology, and diagnostic criteria for AFM and AFP.
- Review of proposed pathogenetic mechanisms and therapeutic strategies.
Main Results:
- AFM is a subset of AFP characterized by specific spinal cord gray matter lesions on MRI.
- AFM impacts spinal cord, brainstem, or motor neuron function, mimicking AFP clinically.
- Distinct features aid in differentiating AFM from AFP and other neurological conditions.
Conclusions:
- AFM diagnosis relies on distinguishing its unique features from AFP and other neurological diseases.
- Understanding the pathogenesis is crucial for developing effective therapies for AFM.
- Continued research is needed to address the growing challenge of AFM in pediatric populations.
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