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A case of chronic inflammatory demyelinating polyradiculoneuropathy after treatment with pegylated interferon α-2a in a patient with chronic hepatitis B virus infection.

Abstract
We report the case of a 42-year-old man with chronic hepatitis B virus infection who developed weakness and paresthesia in the extremities 2 months after administration of pegylated interferon (Peg-IFN)α-2a. Nerve conduction studies conducted 6 months after onset showed abnormal temporal dispersions in both tibial nerves. We diagnosed chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) resulting from treatment with Peg-IFNα-2a. Neurological symptoms were prolonged despite suspension of the treatment. Subsequent treatment with intravenous immunoglobulin improved both clinical symptoms and temporal dispersion. IFNα-induced CIDP is rare, but can reportedly progress even after interruption of IFN-α without immunotherapy. Patients presenting with polyneuropathy after initiation of IFN-α thus require close attention.
AuthorsHiroyuki Naito, Ikuko Takeda, Akiko Segawa, Masataka Tsuge, Hirofumi Maruyama, Masayasu Matsumoto
JournalRinsho shinkeigaku = Clinical neurology (Rinsho Shinkeigaku) Vol. 56 Issue 10 Pg. 672-677 (10 28 2016) ISSN: 1882-0654 [Electronic] Japan
PMID27680223 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Immunoglobulins, Intravenous
  • Interferon-alpha
  • Recombinant Proteins
  • Polyethylene Glycols
  • peginterferon alfa-2a
Topics
  • Adult
  • Chronic Disease
  • Guillain-Barre Syndrome (chemically induced, diet therapy, drug therapy)
  • Hepatitis B, Chronic (drug therapy)
  • Humans
  • Immunoglobulins, Intravenous (therapeutic use)
  • Interferon-alpha (administration & dosage, adverse effects)
  • Male
  • Polyethylene Glycols (administration & dosage, adverse effects)
  • Recombinant Proteins (administration & dosage, adverse effects)
  • Treatment Outcome

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