Charcot-Marie-Tooth (CMT) disease 1A with superimposed inflammatory polyneuropathy in children
Autor(es): Desurkar A,Lin J-P,Mills K,Al-Sarraj S,Jan W,Jungbluth H,Wraige E
Resumo: Charcot-Marie-Tooth (CMT) disease is genetically heterogeneous and subdivided into demyelinating (CMT 1) and axonal (CMT 2) types based on neurophysiology findings. CMT1A, the commonest form associated with duplication of the PMP22 segment on chromosome 17p, often arises in childhood but is generally a slowly progressive disease. We report 2 children presenting with clinical features of an acute inflammatory demyelinating polyneuropathy (AIDP) who were subsequently diagnosed with underlying CMT1A. Both children had neurophysiology and histopathology features consistent with CMT1. Immunoglobulin treatment was initiated considering the evidence of superimposed inflammation and appeared to modify disease progression. Our findings indicate that CMT1A predisposes to a superimposed inflammatory neuropathy. Recognition of this association is difficult, particularly in children without clear family history, but of great importance as immunomodulatory treatment may improve outcome. In addition, we postulate that an underlying genetic polyneuropathy should be suspected if the recovery from AIDP is slower than expected, or incomplete.
Palavras-Chave: Charcot-Marie-Tooth (CMT); CMT1A; Acute inflammatory demyelinating polyneuropathy (AIDP)
Imprenta: Neuropediatrics, v. 40, n. 2, p. 85-88, 2009
Identificador do objeto digital: 10.1055/s-0029-1237720
Descritores: Guillain-Barre Syndrome - Cytopathology ; Guillain-Barre Syndrome - Pathogenesis ; Guillain-Barre Syndrome - Proteins ; Guillain-Barre Syndrome - Inflammation
Data de publicação: 2009