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[Methylprednisolone pulse in treatment of childhood chronic inflammatory demyelinating polyneuropathy]
M A Rafai1, F Z Boulaajaj, Z Sekkat
1Service de neurologie- explorations fonctionnelles, CHU Ibn Rochd, quartier des Hôpitaux, 20000 Casablanca, Maroc. neuroblanca@gmail.com
Abstract:
Chronic inflammatory demyelinating polyneuropathy (CIDP) in children is rare and treatment is based primarily on intravenous immunoglobulins or oral corticosteroids. Boluses of methylprednisolone (MP) are a possible alternative. We report 3 cases of CIDP in children with good outcome after MP pulse therapy. One male (7 years of age) and 2 females (4 and 5 years of age) presented with recurring episodes of functional impotence of both lower limbs and walking impairment, partially reversible without treatment. Clinical and electrophysiological data and the analysis of the cerebrospinal fluid were compatible with CIDP. MP pulses were administered: the total number of pulses varied from 5 to 8, very satisfactory progression on the clinical and electrophysiological pattern was noted, without recurrence in the 3 cases. Childhood CIDP presents clinical, electrophysiological outcome, and prognostic particularities, recurring readily, and the outcome is good. Boluses of MP are an alternative for treatment of these neuropathies in childhood.
Insights
Methylprednisolone (MP) pulse therapy offers a promising alternative for treating pediatric chronic inflammatory demyelinating polyneuropathy (CIDP). This treatment led to good outcomes and no recurrence in three childhood CIDP cases.
Area of Science:
- Pediatric Neurology
- Clinical Electrophysiology
- Immunomodulatory Therapies
Background:
- Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare autoimmune disorder affecting children.
- Current treatments include intravenous immunoglobulins and oral corticosteroids, but alternatives are sought.
- Methylprednisolone (MP) pulse therapy is a potential treatment option for pediatric CIDP.
Observation:
- Three pediatric cases (one male, two females aged 4-7 years) presented with CIDP symptoms.
- Symptoms included recurring lower limb functional impotence and walking impairment.
- Clinical, electrophysiological, and cerebrospinal fluid data confirmed CIDP diagnosis.
Findings:
- All three children received 5-8 pulses of methylprednisolone (MP).
- Patients showed satisfactory clinical and electrophysiological improvement after MP pulse therapy.
- No recurrence of CIDP symptoms was observed in the treated children.
Implications:
- Methylprednisolone (MP) pulse therapy is a viable and effective alternative treatment for childhood CIDP.
- This therapeutic approach demonstrates good outcomes and prevents recurrence in pediatric patients.
- Further research into MP pulse therapy for pediatric neuropathies is warranted.
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