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Schnitzler-Like Syndrome Presenting With IgG Kappa Monoclonal Gammopathy: A Case Report and Review of Diagnostic and Therapeutic Challenges.
Singh, Gurjot; Goswami, Kanishka; Trehan, Shubam; Kachhadia, Meet P; Farooq, Amna; Puri, Piyush; Azhar, Waqas.
Afiliação
  • Singh G; Internal Medicine, Southern Illinois University School of Medicine, Springfield, USA.
  • Goswami K; Internal Medicine, Southern Illinois University School of Medicine, Springfield, USA.
  • Trehan S; Internal Medicine, Southern Illinois University School of Medicine, Springfield, USA.
  • Kachhadia MP; Internal Medicine, Southern Illinois University School of Medicine, Springfield, USA.
  • Farooq A; Internal Medicine, Southern Illinois University School of Medicine, Springfield, USA.
  • Puri P; Internal Medicine, Southern Illinois University School of Medicine, Springfield, USA.
  • Azhar W; Internal Medicine, Memorial Medical Center, Springfield, USA.
Cureus ; 16(7): e64440, 2024 Jul.
Article em En | MEDLINE | ID: mdl-39135817
ABSTRACT
Schnitzler syndrome (SS) is a rare autoinflammatory disorder characterized by a constellation of symptoms that include chronic urticarial rash, recurrent fever, arthralgias/arthritis, and monoclonal gammopathy, typically involving immunoglobulin M (IgM). However, cases with overlapping clinical features but lacking specific criteria fall under the umbrella of Schnitzler-like syndromes. This case report describes a 40-year-old male with Schnitzer-like syndrome and underscores the diagnostic complexities and therapeutic challenges of Schnitzer-like syndrome with IgG kappa monoclonal gammopathy, highlighting the need for a comprehensive diagnostic approach and targeted therapy.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article