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Complication of Hepatitis A Infection: Case Report of Acute Inflammatory Demyelinating Polyneuropathy
Daniel Laursen1, Jeffrey Krug1, Robert Wolford1
1University of Illinois College of Medicine - Peoria, Department of Emergency Medicine, Peoria, Illinois. OSF Saint Francis Medical Center, Department of Emergency Medicine, Peoria, Illinois.
Introduction:
Acute inflammatory demyelinating polyneuropathy (AIDP) is characterized by progressive, mild sensory symptoms and progressive areflexic weakness. It typically follows a gastrointestinal or respiratory infection but has rarely been described after acute viral hepatitis.
Case Report:
This is the case of a 59-year-old male who presented to the emergency department after acutely developing progressive neurologic symptoms following a hospitalization for acute hepatitis A. Cerebrospinal fluid analysis revealed albuminocytologic dissociation, and cervical spine magnetic resonance imaging revealed nerve root enhancement.
Discussion:
The patient was diagnosed with AIDP, which is the most common subtype of Guillain-Barré syndrome in the United States and Europe. There have been few previously reported cases of AIDP following acute hepatitis A infection.
Insights
Acute inflammatory demyelinating polyneuropathy (AIDP), a Guillain-Barré syndrome subtype, rarely follows acute hepatitis A. This case highlights a potential neurological complication of viral hepatitis A, emphasizing the need for awareness among clinicians.
Area of Science:
- Neurology
- Infectious Diseases
- Immunology
Background:
- Acute inflammatory demyelinating polyneuropathy (AIDP) presents with progressive weakness and sensory symptoms.
- AIDP commonly follows infections but is rarely linked to acute viral hepatitis.
- Guillain-Barré syndrome is a significant neurological disorder affecting peripheral nerves.
Purpose of the Study:
- To report a rare case of AIDP following acute hepatitis A.
- To increase awareness of potential neurological complications associated with hepatitis A.
- To contribute to the limited literature on AIDP post-hepatitis A.
Main Methods:
- Case report of a 59-year-old male with acute neurological symptoms.
- Diagnostic procedures included cerebrospinal fluid analysis and MRI.
- Cerebrospinal fluid showed albuminocytologic dissociation, and MRI revealed nerve root enhancement.
Main Results:
- The patient was diagnosed with AIDP.
- Neurological symptoms developed after hospitalization for acute hepatitis A.
- Findings were consistent with demyelination and nerve inflammation.
Conclusions:
- AIDP is the most common Guillain-Barré syndrome subtype in the US and Europe.
- This case adds to the scarce evidence of AIDP occurring after hepatitis A.
- Hepatitis A should be considered as a potential trigger for AIDP.
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