Initial digital vasculitis in a large multicenter cohort of childhood-onset systemic lupus erythematosus

Detalhes bibliográficos
Autor(a) principal: Sakamoto, Ana Paula
Data de Publicação: 2017
Outros Autores: Silva, Clovis Artur, Castro da Silva, Marco Felipe, Lopes, Anandreia Simoes, Souza Russo, Gleice Clemente, Elias Sallum, Adriana Maluf, Kozu, Katia, Bonfa, Eloisa, Saad-Magalhaes, Claudia [UNESP], Rodrigues Pereira, Rosa Maria, Len, Claudio Arnaldo, Terreri, Maria Teresa
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.rbre.2017.09.002
http://hdl.handle.net/11449/163567
Resumo: Objectives: To assess clinical digital vasculitis (DV) as an initial manifestation of childhood onset systemic lupus erythematosus (cSLE) within a large population. Methods: Multicenter cross-sectional study including 852 cSLE patients (ACR criteria) followed in ten Pediatric Rheumatology centers in Sao Paulo State, Brazil. Results: DV was observed in 25/852 (3%) cSLE patients. Periungual hemorrhage was diagnosed in 12 (48%), periungual infarction in 7 (28%), tip finger ulceration in 4 (16%), painful nodules in 1 (4%) and gangrene in 1 (4%). A poor outcome, with digital resorption, occurred in 5 (20%). Comparison of patients with and without DV revealed higher frequency of malar rash (80% vs. 53%, p = 0.008), discoid rash (16% vs. 4%, p = 0.017), photosensitivity (76% vs. 45%, p = 0.002) and other cutaneous vasculitides (80% vs. 19%, p <0.0001), whereas the frequency of overall constitutional features (32% vs. 61%, p = 0.003), fever (32% vs. 56%, p = 0.020) and hepatomegaly (4% vs. 23%, p = 0.026) were lower in these patients. Frequency of female gender, severe multi-organ involvement, autoantibodies profile and low complement were alike in both groups (p >0.05). SLEDAI-2K median, DV descriptor excluded, was significantly lower in patients with DV compared to those without this manifestation [10 (0-28) vs. 14 (0-58), p = 0.004]. Visceral vasculitis or death were not observed in this cSLE cohort. The frequency of cyclophosphamide use (0% vs. 18%, p = 0.014) was significantly lower in the DV group. Conclusion: Our large multicenter study identified clinical DV as one of the rare initial manifestation of active cSLE associated with a mild multisystemic disease, in spite of digital resorption in some of these patients. (C) 2017 Published by Elsevier Editora Ltda.
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spelling Initial digital vasculitis in a large multicenter cohort of childhood-onset systemic lupus erythematosusDigital vasculitisChildhood-onset systemic lupus erythematosusVasculitisSledai-2KObjectives: To assess clinical digital vasculitis (DV) as an initial manifestation of childhood onset systemic lupus erythematosus (cSLE) within a large population. Methods: Multicenter cross-sectional study including 852 cSLE patients (ACR criteria) followed in ten Pediatric Rheumatology centers in Sao Paulo State, Brazil. Results: DV was observed in 25/852 (3%) cSLE patients. Periungual hemorrhage was diagnosed in 12 (48%), periungual infarction in 7 (28%), tip finger ulceration in 4 (16%), painful nodules in 1 (4%) and gangrene in 1 (4%). A poor outcome, with digital resorption, occurred in 5 (20%). Comparison of patients with and without DV revealed higher frequency of malar rash (80% vs. 53%, p = 0.008), discoid rash (16% vs. 4%, p = 0.017), photosensitivity (76% vs. 45%, p = 0.002) and other cutaneous vasculitides (80% vs. 19%, p <0.0001), whereas the frequency of overall constitutional features (32% vs. 61%, p = 0.003), fever (32% vs. 56%, p = 0.020) and hepatomegaly (4% vs. 23%, p = 0.026) were lower in these patients. Frequency of female gender, severe multi-organ involvement, autoantibodies profile and low complement were alike in both groups (p >0.05). SLEDAI-2K median, DV descriptor excluded, was significantly lower in patients with DV compared to those without this manifestation [10 (0-28) vs. 14 (0-58), p = 0.004]. Visceral vasculitis or death were not observed in this cSLE cohort. The frequency of cyclophosphamide use (0% vs. 18%, p = 0.014) was significantly lower in the DV group. Conclusion: Our large multicenter study identified clinical DV as one of the rare initial manifestation of active cSLE associated with a mild multisystemic disease, in spite of digital resorption in some of these patients. (C) 2017 Published by Elsevier Editora Ltda.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Federico FoundationNucleo de Apoio a Pesquisa Saude da Crianca e do Adolescente of USP (NAP-CriAd)Univ Fed Sao Paulo UNIFESP, Unidade Reumatol Pediat, Sao Paulo, SP, BrazilUniv Sao Paulo, Fac Med, Unidade Reumatol Pediat, Sao Paulo, SP, BrazilUniv Sao Paulo, Fac Med, Div Reumatol, Sao Paulo, SP, BrazilUniv Estadual Paulista, UNESP, Fac Med Botucatu, Hosp Clin Botucatu, Botucatu, SP, BrazilUniv Estadual Paulista, UNESP, Fac Med Botucatu, Hosp Clin Botucatu, Botucatu, SP, BrazilCNPq: CNPq 303422/2015-7CNPq: 301805/2013-0CNPq: 305068/2014-8CNPq: 301479/2015CNPq: 303752/2015-7Elsevier B.V.Universidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Sakamoto, Ana PaulaSilva, Clovis ArturCastro da Silva, Marco FelipeLopes, Anandreia SimoesSouza Russo, Gleice ClementeElias Sallum, Adriana MalufKozu, KatiaBonfa, EloisaSaad-Magalhaes, Claudia [UNESP]Rodrigues Pereira, Rosa MariaLen, Claudio ArnaldoTerreri, Maria Teresa2018-11-26T17:42:33Z2018-11-26T17:42:33Z2017-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article583-589application/pdfhttp://dx.doi.org/10.1016/j.rbre.2017.09.002Revista Brasileira De Reumatologia. New York: Elsevier Science Inc, v. 57, n. 6, p. 583-589, 2017.0482-5004http://hdl.handle.net/11449/16356710.1016/j.rbre.2017.09.002WOS:000417146600011WOS000417146600011.pdf70983100083716320000-0002-7631-7093Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengRevista Brasileira De Reumatologia0,340info:eu-repo/semantics/openAccess2023-11-16T06:13:13Zoai:repositorio.unesp.br:11449/163567Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-11-16T06:13:13Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Initial digital vasculitis in a large multicenter cohort of childhood-onset systemic lupus erythematosus
title Initial digital vasculitis in a large multicenter cohort of childhood-onset systemic lupus erythematosus
spellingShingle Initial digital vasculitis in a large multicenter cohort of childhood-onset systemic lupus erythematosus
Sakamoto, Ana Paula
Digital vasculitis
Childhood-onset systemic lupus erythematosus
Vasculitis
Sledai-2K
title_short Initial digital vasculitis in a large multicenter cohort of childhood-onset systemic lupus erythematosus
title_full Initial digital vasculitis in a large multicenter cohort of childhood-onset systemic lupus erythematosus
title_fullStr Initial digital vasculitis in a large multicenter cohort of childhood-onset systemic lupus erythematosus
title_full_unstemmed Initial digital vasculitis in a large multicenter cohort of childhood-onset systemic lupus erythematosus
title_sort Initial digital vasculitis in a large multicenter cohort of childhood-onset systemic lupus erythematosus
author Sakamoto, Ana Paula
author_facet Sakamoto, Ana Paula
Silva, Clovis Artur
Castro da Silva, Marco Felipe
Lopes, Anandreia Simoes
Souza Russo, Gleice Clemente
Elias Sallum, Adriana Maluf
Kozu, Katia
Bonfa, Eloisa
Saad-Magalhaes, Claudia [UNESP]
Rodrigues Pereira, Rosa Maria
Len, Claudio Arnaldo
Terreri, Maria Teresa
author_role author
author2 Silva, Clovis Artur
Castro da Silva, Marco Felipe
Lopes, Anandreia Simoes
Souza Russo, Gleice Clemente
Elias Sallum, Adriana Maluf
Kozu, Katia
Bonfa, Eloisa
Saad-Magalhaes, Claudia [UNESP]
Rodrigues Pereira, Rosa Maria
Len, Claudio Arnaldo
Terreri, Maria Teresa
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Sakamoto, Ana Paula
Silva, Clovis Artur
Castro da Silva, Marco Felipe
Lopes, Anandreia Simoes
Souza Russo, Gleice Clemente
Elias Sallum, Adriana Maluf
Kozu, Katia
Bonfa, Eloisa
Saad-Magalhaes, Claudia [UNESP]
Rodrigues Pereira, Rosa Maria
Len, Claudio Arnaldo
Terreri, Maria Teresa
dc.subject.por.fl_str_mv Digital vasculitis
Childhood-onset systemic lupus erythematosus
Vasculitis
Sledai-2K
topic Digital vasculitis
Childhood-onset systemic lupus erythematosus
Vasculitis
Sledai-2K
description Objectives: To assess clinical digital vasculitis (DV) as an initial manifestation of childhood onset systemic lupus erythematosus (cSLE) within a large population. Methods: Multicenter cross-sectional study including 852 cSLE patients (ACR criteria) followed in ten Pediatric Rheumatology centers in Sao Paulo State, Brazil. Results: DV was observed in 25/852 (3%) cSLE patients. Periungual hemorrhage was diagnosed in 12 (48%), periungual infarction in 7 (28%), tip finger ulceration in 4 (16%), painful nodules in 1 (4%) and gangrene in 1 (4%). A poor outcome, with digital resorption, occurred in 5 (20%). Comparison of patients with and without DV revealed higher frequency of malar rash (80% vs. 53%, p = 0.008), discoid rash (16% vs. 4%, p = 0.017), photosensitivity (76% vs. 45%, p = 0.002) and other cutaneous vasculitides (80% vs. 19%, p <0.0001), whereas the frequency of overall constitutional features (32% vs. 61%, p = 0.003), fever (32% vs. 56%, p = 0.020) and hepatomegaly (4% vs. 23%, p = 0.026) were lower in these patients. Frequency of female gender, severe multi-organ involvement, autoantibodies profile and low complement were alike in both groups (p >0.05). SLEDAI-2K median, DV descriptor excluded, was significantly lower in patients with DV compared to those without this manifestation [10 (0-28) vs. 14 (0-58), p = 0.004]. Visceral vasculitis or death were not observed in this cSLE cohort. The frequency of cyclophosphamide use (0% vs. 18%, p = 0.014) was significantly lower in the DV group. Conclusion: Our large multicenter study identified clinical DV as one of the rare initial manifestation of active cSLE associated with a mild multisystemic disease, in spite of digital resorption in some of these patients. (C) 2017 Published by Elsevier Editora Ltda.
publishDate 2017
dc.date.none.fl_str_mv 2017-11-01
2018-11-26T17:42:33Z
2018-11-26T17:42:33Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.rbre.2017.09.002
Revista Brasileira De Reumatologia. New York: Elsevier Science Inc, v. 57, n. 6, p. 583-589, 2017.
0482-5004
http://hdl.handle.net/11449/163567
10.1016/j.rbre.2017.09.002
WOS:000417146600011
WOS000417146600011.pdf
7098310008371632
0000-0002-7631-7093
url http://dx.doi.org/10.1016/j.rbre.2017.09.002
http://hdl.handle.net/11449/163567
identifier_str_mv Revista Brasileira De Reumatologia. New York: Elsevier Science Inc, v. 57, n. 6, p. 583-589, 2017.
0482-5004
10.1016/j.rbre.2017.09.002
WOS:000417146600011
WOS000417146600011.pdf
7098310008371632
0000-0002-7631-7093
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Revista Brasileira De Reumatologia
0,340
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 583-589
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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