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Stiff-person spectrum disorder induced by shingles: a case report
Sawako Sakai1, Mitsuki Kyoya1, Yuki Kobayashi1
1Department of Neurology, Tsuchiura Kyodo General Hospital, Ibaraki, Japan.
Stiff-person spectrum disorder (SPSD) can be triggered by infections like herpes zoster. Early immunotherapy and pain management are crucial for recovery from infection-related SPSD.
Area of Science:
- Neurology
- Immunology
- Infectious Diseases
Background:
- Stiff-person spectrum disorder (SPSD) is a rare autoimmune neurological condition.
- It presents with progressive rigidity, muscle co-contractions, and spasms.
- A small percentage (5-10%) of SPSD cases are paraneoplastic, with fewer reported infection-related cases.
Purpose of the Study:
- To report a case of SPSD following herpes zoster infection.
- To explore the potential mechanisms linking herpes zoster pain to SPSD exacerbation.
- To highlight the importance of integrated treatment approaches for infection-triggered SPSD.
Main Methods:
- Case study of a 56-year-old female patient.
- Clinical assessment of symptoms including spasms, autonomic dysfunction, and antibody levels.
- Treatment involved immunotherapy (intravenous immunoglobulin, methylprednisolone), benzodiazepines, and epidural analgesia.
Main Results:
- The patient developed SPSD symptoms eight days after herpes zoster rash onset.
- Elevated anti-glutamic acid decarboxylase antibodies were detected in serum and cerebrospinal fluid.
- A 3-month course of immunotherapy and supportive care led to gradual symptom improvement.
Conclusions:
- Herpes zoster pain may worsen SPSD by amplifying muscle co-contractions through reflex pathways.
- Impaired reciprocal inhibition is a key feature of SPSD that can be exacerbated by pain.
- Optimal pain control alongside immunotherapy is recommended for SPSD cases triggered by infection.
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