Schnitzler syndrome associated with MYD88 L265P mutation.

Bashir M, et al.

JAAD Case Rep 5(4):386-388 · 2019

Grade Ccase reportn=1engOpen AccessVerified
DOI ↗PubMed ↗Full Text (PMC) ↗

Abstract

[Abstract not available]

Key Findings

  • ●First reported case with MYD88 L265P
  • ●Proposed MYD88 as link to Waldenström's
  • ●Near-complete remission on anakinra

Subject Classification

EM, erythema multiformeKD, Kawasaki diseaseKawasakiSJS, Steven-Johnson syndromeerythema multiformemucocutaneous lymph node syndromestreptococcal pharyngitisstreptococcus pyogenesvasculitis

Referenced in (1 disease)

Schnitzler Syndrome

Validation history

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  1. passsource metadataJun 1, 2026, 04:40 PMby pubmed-api

    Identifier corrected: prior entry (pmid-31008176) had a wrong PMID/DOI pointing to an unrelated paper; re-resolved by title to this record via PubMed/Crossref.

    tools: pubmed.esummary, crossref.works

ID: pmid-30989098DOI: 10.1016/j.jdcr.2019.02.002PMID: 30989098PMCID: PMC6454123