Malignant Evolution of Schnitzler Syndrome to Waldenström Macroglobulinemia: a Case Report

Introduction: Schnitzler syndrome (SchS), first described in 1972, is a rare autoinflammatory condition characterized by chronic urticaria and monoclonal gammopathy of IgM or, exceptionally, IgG profile. Additional features include recurrent fever, evidence of abnormal bone remodeling, a neutrophili...

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Main Authors: Man Cristina-Alexandra, László Nimród, Horváth Emőke, Demian Smaranda
Format: Article
Language:English
Published: Sciendo 2022-09-01
Series:Journal of Interdisciplinary Medicine
Subjects:
Online Access:https://doi.org/10.2478/jim-2022-0011
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author Man Cristina-Alexandra
László Nimród
Horváth Emőke
Demian Smaranda
author_facet Man Cristina-Alexandra
László Nimród
Horváth Emőke
Demian Smaranda
author_sort Man Cristina-Alexandra
collection DOAJ
description Introduction: Schnitzler syndrome (SchS), first described in 1972, is a rare autoinflammatory condition characterized by chronic urticaria and monoclonal gammopathy of IgM or, exceptionally, IgG profile. Additional features include recurrent fever, evidence of abnormal bone remodeling, a neutrophilic dermal infiltrate on skin biopsy, leukocytosis or elevated C-reactive protein, according to the Strasbourg criteria.
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spelling doaj.art-bf4160cec4134b9c95962d0f1d9c88202022-12-22T03:45:29ZengSciendoJournal of Interdisciplinary Medicine2501-81322022-09-0173747710.2478/jim-2022-0011Malignant Evolution of Schnitzler Syndrome to Waldenström Macroglobulinemia: a Case ReportMan Cristina-Alexandra0László Nimród1Horváth Emőke2Demian Smaranda3Pneumology Clinic, County Clinical Hospital, Târgu Mureș, RomaniaPneumology Clinic, County Clinical Hospital, Târgu Mureș, RomaniaDepartment of Morphopathology, Emergency County Clinical Hospital, Târgu Mureș, Romania“George Emil Palade” University of Medicine, Pharmacy, Science and Technology, Târgu Mureș, RomaniaIntroduction: Schnitzler syndrome (SchS), first described in 1972, is a rare autoinflammatory condition characterized by chronic urticaria and monoclonal gammopathy of IgM or, exceptionally, IgG profile. Additional features include recurrent fever, evidence of abnormal bone remodeling, a neutrophilic dermal infiltrate on skin biopsy, leukocytosis or elevated C-reactive protein, according to the Strasbourg criteria.https://doi.org/10.2478/jim-2022-0011schnitzler syndromewaldenström macroglobulinemiaigm monoclonal gammopathyautoinflammatory diseasechronic urticaria
spellingShingle Man Cristina-Alexandra
László Nimród
Horváth Emőke
Demian Smaranda
Malignant Evolution of Schnitzler Syndrome to Waldenström Macroglobulinemia: a Case Report
Journal of Interdisciplinary Medicine
schnitzler syndrome
waldenström macroglobulinemia
igm monoclonal gammopathy
autoinflammatory disease
chronic urticaria
title Malignant Evolution of Schnitzler Syndrome to Waldenström Macroglobulinemia: a Case Report
title_full Malignant Evolution of Schnitzler Syndrome to Waldenström Macroglobulinemia: a Case Report
title_fullStr Malignant Evolution of Schnitzler Syndrome to Waldenström Macroglobulinemia: a Case Report
title_full_unstemmed Malignant Evolution of Schnitzler Syndrome to Waldenström Macroglobulinemia: a Case Report
title_short Malignant Evolution of Schnitzler Syndrome to Waldenström Macroglobulinemia: a Case Report
title_sort malignant evolution of schnitzler syndrome to waldenstrom macroglobulinemia a case report
topic schnitzler syndrome
waldenström macroglobulinemia
igm monoclonal gammopathy
autoinflammatory disease
chronic urticaria
url https://doi.org/10.2478/jim-2022-0011
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AT laszlonimrod malignantevolutionofschnitzlersyndrometowaldenstrommacroglobulinemiaacasereport
AT horvathemoke malignantevolutionofschnitzlersyndrometowaldenstrommacroglobulinemiaacasereport
AT demiansmaranda malignantevolutionofschnitzlersyndrometowaldenstrommacroglobulinemiaacasereport