Schnitzler syndrome: validation and applicability of diagnostic criteria in real‐life patients

Background Schnitzler syndrome is characterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological signs of neutrophil‐mediated inflammation. The aim of this study was to assess the applicability and validity of the existing diagnostic criteria in real‐life pa...

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Published inAllergy (Copenhagen) Vol. 72; no. 2; pp. 177 - 182
Main Authors Gusdorf, L., Asli, B., Barbarot, S., Néel, A., Masseau, A., Puéchal, X., Gottenberg, J‐E., Grateau, G., Blanchard‐Delaunay, C., Rizzi, R., Lifermann, F., Kyndt, X., Aubin, F., Bessis, D., Boye, T., Gayet, S., Rongioletti, F., Sauleau, E., Fermand, J‐P., Lipsker, D.
Format Journal Article
LanguageEnglish
Published Denmark Blackwell Publishing Ltd 01.02.2017
Wiley
Subjects
Online AccessGet full text
ISSN0105-4538
1398-9995
1398-9995
DOI10.1111/all.13035

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Abstract Background Schnitzler syndrome is characterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological signs of neutrophil‐mediated inflammation. The aim of this study was to assess the applicability and validity of the existing diagnostic criteria in real‐life patients. Methods This multicentric study was conducted between 2009 and 2014 in 14 hospitals in which patients with Schnitzler syndrome or controls with related disorders were followed up. We compared the sensitivities and specificities and calculated the positive and negative predictive values of the Lipsker and of the Strasbourg criteria for the patients with Schnitzler syndrome and for the controls. We included 42 patients with Schnitzler syndrome, 12 with adult‐onset Still's disease, 7 with cryopyrin‐associated periodic disease, 9 with Waldenström disease, and 10 with chronic spontaneous urticaria. Results All patients with Schnitzler syndrome met the Lipsker criteria. According to the Strasbourg criteria, 34 patients had definite Schnitzler syndrome, five had probable Schnitzler syndrome, and three did not meet the criteria. One control met the Lipsker criteria and had probable Schnitzler syndrome according to the Strasbourg criteria. Sensitivity and specificity of the Lipsker criteria were 100% and 97%, respectively. For the Strasbourg criteria, sensitivity for definite and probable diagnosis was 81% and 93%, respectively, with a corresponding specificity of 100% and 97%. Conclusion Diagnostic criteria currently in use to diagnose Schnitzler syndrome are reliable. More investigations must be done to attest their efficiency in patients with recent‐onset manifestations.
AbstractList Schnitzler syndrome is characterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological signs of neutrophil-mediated inflammation. The aim of this study was to assess the applicability and validity of the existing diagnostic criteria in real-life patients.BACKGROUNDSchnitzler syndrome is characterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological signs of neutrophil-mediated inflammation. The aim of this study was to assess the applicability and validity of the existing diagnostic criteria in real-life patients.This multicentric study was conducted between 2009 and 2014 in 14 hospitals in which patients with Schnitzler syndrome or controls with related disorders were followed up. We compared the sensitivities and specificities and calculated the positive and negative predictive values of the Lipsker and of the Strasbourg criteria for the patients with Schnitzler syndrome and for the controls. We included 42 patients with Schnitzler syndrome, 12 with adult-onset Still's disease, 7 with cryopyrin-associated periodic disease, 9 with Waldenström disease, and 10 with chronic spontaneous urticaria.METHODSThis multicentric study was conducted between 2009 and 2014 in 14 hospitals in which patients with Schnitzler syndrome or controls with related disorders were followed up. We compared the sensitivities and specificities and calculated the positive and negative predictive values of the Lipsker and of the Strasbourg criteria for the patients with Schnitzler syndrome and for the controls. We included 42 patients with Schnitzler syndrome, 12 with adult-onset Still's disease, 7 with cryopyrin-associated periodic disease, 9 with Waldenström disease, and 10 with chronic spontaneous urticaria.All patients with Schnitzler syndrome met the Lipsker criteria. According to the Strasbourg criteria, 34 patients had definite Schnitzler syndrome, five had probable Schnitzler syndrome, and three did not meet the criteria. One control met the Lipsker criteria and had probable Schnitzler syndrome according to the Strasbourg criteria. Sensitivity and specificity of the Lipsker criteria were 100% and 97%, respectively. For the Strasbourg criteria, sensitivity for definite and probable diagnosis was 81% and 93%, respectively, with a corresponding specificity of 100% and 97%.RESULTSAll patients with Schnitzler syndrome met the Lipsker criteria. According to the Strasbourg criteria, 34 patients had definite Schnitzler syndrome, five had probable Schnitzler syndrome, and three did not meet the criteria. One control met the Lipsker criteria and had probable Schnitzler syndrome according to the Strasbourg criteria. Sensitivity and specificity of the Lipsker criteria were 100% and 97%, respectively. For the Strasbourg criteria, sensitivity for definite and probable diagnosis was 81% and 93%, respectively, with a corresponding specificity of 100% and 97%.Diagnostic criteria currently in use to diagnose Schnitzler syndrome are reliable. More investigations must be done to attest their efficiency in patients with recent-onset manifestations.CONCLUSIONDiagnostic criteria currently in use to diagnose Schnitzler syndrome are reliable. More investigations must be done to attest their efficiency in patients with recent-onset manifestations.
Background: Schnitzler syndrome is characterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological signs of neutrophil-mediated inflammation. The aim of this study was to assess the applicability and validity of the existing diagnostic criteria in real-life patients.Methods: This multicentric study was conducted between 2009 and 2014 in 14 hospitals in which patients with Schnitzler syndrome or controls with related disorders were followed up. We compared the sensitivities and specificities and calculated the positive and negative predictive values of the Lipsker and of the Strasbourg criteria for the patients with Schnitzler syndrome and for the controls. We included 42 patients with Schnitzler syndrome, 12 with adult-onset Still's disease, 7 with cryopyrin-associated periodic disease, 9 with Waldenström disease, and 10 with chronic spontaneous urticaria.Results: All patients with Schnitzler syndrome met the Lipsker criteria. According to the Strasbourg criteria, 34 patients had definite Schnitzler syndrome, five had probable Schnitzler syndrome, and three did not meet the criteria. One control met the Lipsker criteria and had probable Schnitzler syndrome according to the Strasbourg criteria. Sensitivity and specificity of the Lipsker criteria were 100% and 97%, respectively. For the Strasbourg criteria, sensitivity for definite and probable diagnosis was 81% and 93%, respectively, with a corresponding specificity of 100% and 97%.Conclusion: Diagnostic criteria currently in use to diagnose Schnitzler syndrome are reliable. More investigations must be done to attest their efficiency in patients with recent-onset manifestations.
Background Schnitzler syndrome is characterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological signs of neutrophil-mediated inflammation. The aim of this study was to assess the applicability and validity of the existing diagnostic criteria in real-life patients. Methods This multicentric study was conducted between 2009 and 2014 in 14 hospitals in which patients with Schnitzler syndrome or controls with related disorders were followed up. We compared the sensitivities and specificities and calculated the positive and negative predictive values of the Lipsker and of the Strasbourg criteria for the patients with Schnitzler syndrome and for the controls. We included 42 patients with Schnitzler syndrome, 12 with adult-onset Still's disease, 7 with cryopyrin-associated periodic disease, 9 with Waldenstrom disease, and 10 with chronic spontaneous urticaria. Results All patients with Schnitzler syndrome met the Lipsker criteria. According to the Strasbourg criteria, 34 patients had definite Schnitzler syndrome, five had probable Schnitzler syndrome, and three did not meet the criteria. One control met the Lipsker criteria and had probable Schnitzler syndrome according to the Strasbourg criteria. Sensitivity and specificity of the Lipsker criteria were 100% and 97%, respectively. For the Strasbourg criteria, sensitivity for definite and probable diagnosis was 81% and 93%, respectively, with a corresponding specificity of 100% and 97%. Conclusion Diagnostic criteria currently in use to diagnose Schnitzler syndrome are reliable. More investigations must be done to attest their efficiency in patients with recent-onset manifestations.
Schnitzler syndrome is characterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological signs of neutrophil-mediated inflammation. The aim of this study was to assess the applicability and validity of the existing diagnostic criteria in real-life patients. This multicentric study was conducted between 2009 and 2014 in 14 hospitals in which patients with Schnitzler syndrome or controls with related disorders were followed up. We compared the sensitivities and specificities and calculated the positive and negative predictive values of the Lipsker and of the Strasbourg criteria for the patients with Schnitzler syndrome and for the controls. We included 42 patients with Schnitzler syndrome, 12 with adult-onset Still's disease, 7 with cryopyrin-associated periodic disease, 9 with Waldenström disease, and 10 with chronic spontaneous urticaria. All patients with Schnitzler syndrome met the Lipsker criteria. According to the Strasbourg criteria, 34 patients had definite Schnitzler syndrome, five had probable Schnitzler syndrome, and three did not meet the criteria. One control met the Lipsker criteria and had probable Schnitzler syndrome according to the Strasbourg criteria. Sensitivity and specificity of the Lipsker criteria were 100% and 97%, respectively. For the Strasbourg criteria, sensitivity for definite and probable diagnosis was 81% and 93%, respectively, with a corresponding specificity of 100% and 97%. Diagnostic criteria currently in use to diagnose Schnitzler syndrome are reliable. More investigations must be done to attest their efficiency in patients with recent-onset manifestations.
Background Schnitzler syndrome is characterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological signs of neutrophil‐mediated inflammation. The aim of this study was to assess the applicability and validity of the existing diagnostic criteria in real‐life patients. Methods This multicentric study was conducted between 2009 and 2014 in 14 hospitals in which patients with Schnitzler syndrome or controls with related disorders were followed up. We compared the sensitivities and specificities and calculated the positive and negative predictive values of the Lipsker and of the Strasbourg criteria for the patients with Schnitzler syndrome and for the controls. We included 42 patients with Schnitzler syndrome, 12 with adult‐onset Still's disease, 7 with cryopyrin‐associated periodic disease, 9 with Waldenström disease, and 10 with chronic spontaneous urticaria. Results All patients with Schnitzler syndrome met the Lipsker criteria. According to the Strasbourg criteria, 34 patients had definite Schnitzler syndrome, five had probable Schnitzler syndrome, and three did not meet the criteria. One control met the Lipsker criteria and had probable Schnitzler syndrome according to the Strasbourg criteria. Sensitivity and specificity of the Lipsker criteria were 100% and 97%, respectively. For the Strasbourg criteria, sensitivity for definite and probable diagnosis was 81% and 93%, respectively, with a corresponding specificity of 100% and 97%. Conclusion Diagnostic criteria currently in use to diagnose Schnitzler syndrome are reliable. More investigations must be done to attest their efficiency in patients with recent‐onset manifestations.
Author Barbarot, S.
Fermand, J‐P.
Néel, A.
Puéchal, X.
Gottenberg, J‐E.
Rongioletti, F.
Gusdorf, L.
Masseau, A.
Rizzi, R.
Asli, B.
Grateau, G.
Lifermann, F.
Sauleau, E.
Gayet, S.
Bessis, D.
Aubin, F.
Boye, T.
Kyndt, X.
Blanchard‐Delaunay, C.
Lipsker, D.
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/27564982$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1186/s13075-015-0696-0
10.1016/j.jaci.2014.07.050
10.1016/j.idc.2007.08.004
10.1111/j.1600-0560.2010.01638.x
10.1111/j.1346-8138.2002.tb00212.x
10.1046/j.1440-0960.1999.00361.x
10.1097/00005792-200101000-00004
10.1111/all.12129
10.1186/2045-7022-4-41
10.1111/j.1365-2133.1995.tb02507.x
10.2214/ajr.175.5.1751325
10.3324/haematol.2012.067306
10.1097/MD.0b013e3181943f5e
10.1007/s00256-006-0093-5
10.2307/271031
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Copyright © 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
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Issue 2
Keywords diagnostic criteria
neutrophilic urticarial dermatosis
auto-inflammatory disease
Schnitzler syndrome
monoclonal gammopathy
Language English
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2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
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References 2001; 80
2009; 88
1989; 116
2015; 17
2014; 4
2002; 29
2011
2013; 68
2015; 135
1992; 19
1972
2000; 175
1999; 40
1995; 133
2011; 38
2007; 21
1987; 17
2007; 36
2012; 97
Kieffer (10.1111/all.13035-BIB0010|all13035-cit-0010) 2009; 88
Welsh (10.1111/all.13035-BIB0003|all13035-cit-0003) 1999; 40
Terpos (10.1111/all.13035-BIB0016|all13035-cit-0016) 2012; 97
De Koning (10.1111/all.13035-BIB0017|all13035-cit-0017) 2015; 135
Simon (10.1111/all.13035-BIB0005|all13035-cit-0005) 2013; 68
De Koning (10.1111/all.13035-BIB0019|all13035-cit-0019) 2014; 4
Schnitzler (10.1111/all.13035-BIB0001|all13035-cit-0001) 1972
Rubin (10.1111/all.13035-BIB0008|all13035-cit-0008) 1987; 17
Zhou (10.1111/all.13035-BIB0009|all13035-cit-0009) 2011
Kolivras (10.1111/all.13035-BIB0011|all13035-cit-0011) 2011; 38
De Waele (10.1111/all.13035-BIB0014|all13035-cit-0014) 2000; 175
Nashan (10.1111/all.13035-BIB0006|all13035-cit-0006) 1995; 133
Yamaguchi (10.1111/all.13035-BIB0007|all13035-cit-0007) 1992; 19
Schnitzler (10.1111/all.13035-BIB0013|all13035-cit-0013) 1989; 116
Lipsker (10.1111/all.13035-BIB0004|all13035-cit-0004) 2001; 80
Akimoto (10.1111/all.13035-BIB0002|all13035-cit-0002) 2002; 29
De Koning (10.1111/all.13035-BIB0018|all13035-cit-0018) 2015; 17
Bertrand (10.1111/all.13035-BIB0015|all13035-cit-0015) 2007; 36
Knockaert (10.1111/all.13035-BIB0012|all13035-cit-0012) 2007; 21
References_xml – year: 2011
– volume: 88
  start-page: 23
  year: 2009
  end-page: 31
  article-title: Neutrophilic urticarial dermatosis: a variant of neutrophilic urticaria strongly associated with systemic disease. Report of 9 new cases and review of the literature
  publication-title: Medicine (Balt)
– year: 1972
  article-title: Lésions urticariennes chroniques permanentes (érythème pétaloïde?)
  publication-title: Journée Dermatologique d'Angers
– volume: 68
  start-page: 562
  year: 2013
  end-page: 568
  article-title: Schnitzler's syndrome: diagnosis, treatment, and follow‐up
  publication-title: Allergy
– volume: 97
  start-page: 1699
  year: 2012
  end-page: 1703
  article-title: Increased angiogenesis and enhanced bone formation in patients with IgM monoclonal gammopathy and urticarial skin rash: new insight into the biology of Schnitzler syndrome
  publication-title: Haematologica
– volume: 80
  start-page: 37
  year: 2001
  end-page: 44
  article-title: The Schnitzler syndrome. Four new cases and review of the literature
  publication-title: Medicine (Balt)
– volume: 29
  start-page: 735
  year: 2002
  end-page: 738
  article-title: Schnitzler's syndrome with IgG kappa gammopathy
  publication-title: J Dermatol
– volume: 175
  start-page: 1325
  year: 2000
  end-page: 1327
  article-title: Schnitzler's syndrome: an unusual cause of bone pain with suggestive imaging features
  publication-title: AJR Am J Roentgenol
– volume: 4
  start-page: 41
  year: 2014
  article-title: Schnitzler's syndrome: lessons from 281 cases
  publication-title: Clin Transl Allergy
– volume: 116
  start-page: 547
  year: 1989
  end-page: 550
  article-title: Chronic urticaria–osteo‐condensation–macroglobulinemia. Principal case. Study of 20 cases
  publication-title: Ann Dermatol Venereol
– volume: 36
  start-page: 153
  year: 2007
  end-page: 156
  article-title: Schnitzler's syndrome: 3‐year radiological follow‐up
  publication-title: Skeletal Radiol
– volume: 135
  start-page: 561
  year: 2015
  end-page: 564
  article-title: Myeloid lineage‐restricted somatic mosaicism of NLRP3 mutations in patients with variant Schnitzler syndrome
  publication-title: J Allergy Clin Immunol
– volume: 19
  start-page: 424
  year: 1992
  end-page: 430
  article-title: Preliminary criteria for classification of adult Still's disease
  publication-title: J Rheumatol
– volume: 17
  start-page: 131
  year: 1987
  end-page: 144
  article-title: Logit‐based interval estimation for binomial data using the Jeffreys prior
  publication-title: Sociol Methodol
– volume: 40
  start-page: 201
  year: 1999
  end-page: 203
  article-title: Schnitzler's syndrome: report of a case with progression to Waldenstrom's macroglobulinaemia
  publication-title: Australas J Dermatol
– volume: 21
  start-page: 1189
  year: 2007
  end-page: 1211
  article-title: Recurrent fevers of unknown origin
  publication-title: Infect Dis Clin North Am
– volume: 38
  start-page: 202
  year: 2011
  end-page: 208
  article-title: Cryopyrin‐associated periodic syndrome: an autoinflammatory disease manifested as neutrophilic urticarial dermatosis with additional perieccrine involvement
  publication-title: J Cutan Pathol
– volume: 133
  start-page: 132
  year: 1995
  end-page: 134
  article-title: Chronic urticaria, arthralgia, raised erythrocyte sedimentation rate and IgG paraproteinaemia: a variant of Schnitzler's syndrome?
  publication-title: Br J Dermatol
– volume: 17
  start-page: 187
  year: 2015
  article-title: The role of interleukin‐1 beta in the pathophysiology of Schnitzler's syndrome
  publication-title: Arthritis Res Ther
– volume: 17
  start-page: 187
  year: 2015
  ident: 10.1111/all.13035-BIB0018|all13035-cit-0018
  article-title: The role of interleukin-1 beta in the pathophysiology of Schnitzler's syndrome
  publication-title: Arthritis Res Ther
  doi: 10.1186/s13075-015-0696-0
– volume: 135
  start-page: 561
  year: 2015
  ident: 10.1111/all.13035-BIB0017|all13035-cit-0017
  article-title: Myeloid lineage-restricted somatic mosaicism of NLRP3 mutations in patients with variant Schnitzler syndrome
  publication-title: J Allergy Clin Immunol
  doi: 10.1016/j.jaci.2014.07.050
– volume: 21
  start-page: 1189
  year: 2007
  ident: 10.1111/all.13035-BIB0012|all13035-cit-0012
  article-title: Recurrent fevers of unknown origin
  publication-title: Infect Dis Clin North Am
  doi: 10.1016/j.idc.2007.08.004
– volume: 38
  start-page: 202
  year: 2011
  ident: 10.1111/all.13035-BIB0011|all13035-cit-0011
  article-title: Cryopyrin-associated periodic syndrome: an autoinflammatory disease manifested as neutrophilic urticarial dermatosis with additional perieccrine involvement
  publication-title: J Cutan Pathol
  doi: 10.1111/j.1600-0560.2010.01638.x
– volume: 29
  start-page: 735
  year: 2002
  ident: 10.1111/all.13035-BIB0002|all13035-cit-0002
  article-title: Schnitzler's syndrome with IgG kappa gammopathy
  publication-title: J Dermatol
  doi: 10.1111/j.1346-8138.2002.tb00212.x
– volume: 40
  start-page: 201
  year: 1999
  ident: 10.1111/all.13035-BIB0003|all13035-cit-0003
  article-title: Schnitzler's syndrome: report of a case with progression to Waldenstrom's macroglobulinaemia
  publication-title: Australas J Dermatol
  doi: 10.1046/j.1440-0960.1999.00361.x
– volume: 80
  start-page: 37
  year: 2001
  ident: 10.1111/all.13035-BIB0004|all13035-cit-0004
  article-title: The Schnitzler syndrome. Four new cases and review of the literature
  publication-title: Medicine (Balt)
  doi: 10.1097/00005792-200101000-00004
– volume: 68
  start-page: 562
  year: 2013
  ident: 10.1111/all.13035-BIB0005|all13035-cit-0005
  article-title: Schnitzler's syndrome: diagnosis, treatment, and follow-up
  publication-title: Allergy
  doi: 10.1111/all.12129
– volume: 116
  start-page: 547
  year: 1989
  ident: 10.1111/all.13035-BIB0013|all13035-cit-0013
  article-title: Chronic urticaria-osteo-condensation-macroglobulinemia. Principal case. Study of 20 cases
  publication-title: Ann Dermatol Venereol
– volume: 4
  start-page: 41
  year: 2014
  ident: 10.1111/all.13035-BIB0019|all13035-cit-0019
  article-title: Schnitzler's syndrome: lessons from 281 cases
  publication-title: Clin Transl Allergy
  doi: 10.1186/2045-7022-4-41
– volume: 133
  start-page: 132
  year: 1995
  ident: 10.1111/all.13035-BIB0006|all13035-cit-0006
  article-title: Chronic urticaria, arthralgia, raised erythrocyte sedimentation rate and IgG paraproteinaemia: a variant of Schnitzler's syndrome?
  publication-title: Br J Dermatol
  doi: 10.1111/j.1365-2133.1995.tb02507.x
– volume: 175
  start-page: 1325
  year: 2000
  ident: 10.1111/all.13035-BIB0014|all13035-cit-0014
  article-title: Schnitzler's syndrome: an unusual cause of bone pain with suggestive imaging features
  publication-title: AJR Am J Roentgenol
  doi: 10.2214/ajr.175.5.1751325
– volume-title: Wiley Series in Probability and Statistics
  year: 2011
  ident: 10.1111/all.13035-BIB0009|all13035-cit-0009
– volume: 97
  start-page: 1699
  year: 2012
  ident: 10.1111/all.13035-BIB0016|all13035-cit-0016
  article-title: Increased angiogenesis and enhanced bone formation in patients with IgM monoclonal gammopathy and urticarial skin rash: new insight into the biology of Schnitzler syndrome
  publication-title: Haematologica
  doi: 10.3324/haematol.2012.067306
– volume: 88
  start-page: 23
  year: 2009
  ident: 10.1111/all.13035-BIB0010|all13035-cit-0010
  article-title: Neutrophilic urticarial dermatosis: a variant of neutrophilic urticaria strongly associated with systemic disease. Report of 9 new cases and review of the literature
  publication-title: Medicine (Balt)
  doi: 10.1097/MD.0b013e3181943f5e
– volume: 36
  start-page: 153
  year: 2007
  ident: 10.1111/all.13035-BIB0015|all13035-cit-0015
  article-title: Schnitzler's syndrome: 3-year radiological follow-up
  publication-title: Skeletal Radiol
  doi: 10.1007/s00256-006-0093-5
– year: 1972
  ident: 10.1111/all.13035-BIB0001|all13035-cit-0001
  article-title: Lésions urticariennes chroniques permanentes (érythème pétaloïde?)
  publication-title: Journée Dermatologique d'Angers
– volume: 17
  start-page: 131
  year: 1987
  ident: 10.1111/all.13035-BIB0008|all13035-cit-0008
  article-title: Logit-based interval estimation for binomial data using the Jeffreys prior
  publication-title: Sociol Methodol
  doi: 10.2307/271031
– volume: 19
  start-page: 424
  year: 1992
  ident: 10.1111/all.13035-BIB0007|all13035-cit-0007
  article-title: Preliminary criteria for classification of adult Still's disease
  publication-title: J Rheumatol
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Snippet Background Schnitzler syndrome is characterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological signs of...
Schnitzler syndrome is characterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological signs of neutrophil-mediated...
Background Schnitzler syndrome is characterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological signs of...
Background: Schnitzler syndrome is characterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological signs of...
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StartPage 177
SubjectTerms Adolescent
Adult
auto‐inflammatory disease
Child
Child, Preschool
diagnostic criteria
Female
Humans
Immunology
Innate immunity
Life Sciences
Male
Medical diagnosis
Medical treatment
monoclonal gammopathy
neutrophilic urticarial dermatosis
Reproducibility of Results
Schnitzler syndrome
Schnitzler Syndrome - diagnosis
Sensitivity and Specificity
Severity of Illness Index
Skin diseases
Symptom Assessment
Young Adult
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Title Schnitzler syndrome: validation and applicability of diagnostic criteria in real‐life patients
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