Abstract
Myasthenia gravis is among the rare complications after allogeneic hematopoietic stem cell transplantation and is usually associated with chronic GVHD. Herein, we report a 2-year and 10 months of age female with Griscelli syndrome, who developed severe myasthenia gravis at post-transplant +22nd month and required respiratory support with mechanical ventilation. She was unresponsive to cyclosporine A, methylprednisolone, intravenous immunoglobulin, and mycophenolate mofetil and the symptoms could only be controlled after plasma exchange and subsequent use of rituximab, in addition to cyclosporine A and mycophenolate mofetil maintenance. She is currently asymptomatic on the 6th month of follow-up.
Keywords:
Griscelli syndrome; bone marrow transplantation; graft-versus-host disease; myasthenia gravis; plasma exchange; rituximab.
© 2013 Wiley Periodicals, Inc.
MeSH terms
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Antibodies, Monoclonal, Murine-Derived / therapeutic use*
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Antineoplastic Agents / therapeutic use*
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Combined Modality Therapy
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Cyclosporine / therapeutic use
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Female
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Graft vs Host Disease / etiology
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Graft vs Host Disease / therapy
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Hearing Loss, Sensorineural / complications
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Hearing Loss, Sensorineural / therapy*
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Hematopoietic Stem Cell Transplantation / adverse effects*
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Humans
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Immunosuppressive Agents / therapeutic use
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Infant
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Myasthenia Gravis / diagnosis
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Myasthenia Gravis / etiology
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Myasthenia Gravis / therapy*
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Mycophenolic Acid / analogs & derivatives
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Mycophenolic Acid / therapeutic use
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Piebaldism / complications
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Piebaldism / therapy*
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Pigmentation Disorders / complications
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Pigmentation Disorders / therapy*
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Plasma Exchange*
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Remission Induction
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Rituximab
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Transplantation, Homologous
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Treatment Outcome
Substances
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Antibodies, Monoclonal, Murine-Derived
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Antineoplastic Agents
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Immunosuppressive Agents
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Rituximab
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Cyclosporine
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Mycophenolic Acid
Supplementary concepts
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Griscelli syndrome type 1