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A 2-Year-Old Boy With Difficulty Waking After Bone Marrow Transplantation.
Eileen Broomall1, John Michael Taylor1, Katrina Peariso1
1From the Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Seminars in Pediatric Neurology
|July 3, 2018
Summary
A bone marrow transplant for Wiskott-Aldrich syndrome led to a rare neurological complication, Guillain-Barre syndrome, in a young boy. Prompt immunotherapy resulted in gradual motor recovery over several months.
Area of Science:
- Pediatric Neurology
- Hematology
- Immunology
Background:
- Wiskott-Aldrich syndrome is a rare primary immunodeficiency requiring bone marrow transplantation.
- Bone marrow transplantation can lead to various immune-mediated complications.
- Prolonged intensive care unit stays can present diagnostic challenges for neurological complications.
Observation:
- A 2-year-old boy developed neurological symptoms including nuchal rigidity, decreased movement, and areflexia during intensive care.
- Electromyography revealed a length-dependent, axonal, sensorimotor polyneuropathy.
- Cerebrospinal fluid analysis showed albuminocytologic dissociation.
Findings:
- The patient's presentation was suggestive of Guillain-Barre syndrome or its variant, acute motor and sensory axonal neuropathy.
- The neurological deficit developed during intensive care admission following bone marrow transplant.
- The patient experienced slow motor recovery over several months with immunotherapy.
Implications:
- This case highlights a rare neurological complication post-bone marrow transplant for Wiskott-Aldrich syndrome.
- Early recognition and immunotherapy are crucial for managing such immune-mediated neurological disorders.
- Understanding these complications is vital for optimizing care in pediatric transplant recipients.
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