Clinical presentation and salivary gland histopathology of paediatric primary Sjögren's syndrome

Detalhes bibliográficos
Autor(a) principal: Saad-Magalhães, Claudia [UNESP]
Data de Publicação: 2011
Outros Autores: De Souza Medeiros, P. B. [UNESP], Oliveira Sato, J. [UNESP], Custódio Domingues, M. A. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://hdl.handle.net/11449/226489
Resumo: Objective: Explore the presentation, diagnostic criteria and exocrine gland histopathology of paediatric primary Sjögren's syndrome (PPSjS). Methods: A case series of 8 children is reported and American-European Consensus Group (AECG-2002) criteria were examined, as well as minor labial salivary and lachrymal gland biopsies, which were scored by a pathologist blinded to outcome. For all cases, connective tissue diseases and parotid-related infectious disease were excluded. Results: Age at onset varied from 5-13 years old; 6 were females, all followed from diagnosis up to the last visit (1-10 years). The main features at presentation were recurrent tender parotid swelling and sialectasis imaging, with decreased salivary function assessed by Tc-99 scintigraphy. Mild sicca symptoms were observed in 4/8 cases. Systemic features, including fatigue, myalgia, arthritis, tenosynovitis, joint contractures, transient Raynaud's and high ESR, were recorded at onset. Autoantibody profile was unremarkable for diagnosis, while lymphocytic infiltration of labial salivary glands and sialectasis were observed in all biopsies (8/8). In lachrymal glands, massive lymphocytic infiltration and lymphocytic gastritis were observed during complementary assessment. Flares were treated with low dose steroids and long-term use of hydroxychloroquine (5/8), although only 3/8 fulfilled AECG-2002 diagnostic criteria, throughout the disease course. Conclusion: PPSjS is rare, slowly progressive and its early presentation is variable. Standardised diagnostic algorithms should include recurrent parotid swelling and early diagnosis should rely mostly on salivary and lachrymal gland histopathology in this age group. © Copyright Clinical and Experimental Rheumatology 2011.
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spelling Clinical presentation and salivary gland histopathology of paediatric primary Sjögren's syndromeChildrenFocal sialadenitisRecurrent parotitisSialectasisSjögren's syndromeObjective: Explore the presentation, diagnostic criteria and exocrine gland histopathology of paediatric primary Sjögren's syndrome (PPSjS). Methods: A case series of 8 children is reported and American-European Consensus Group (AECG-2002) criteria were examined, as well as minor labial salivary and lachrymal gland biopsies, which were scored by a pathologist blinded to outcome. For all cases, connective tissue diseases and parotid-related infectious disease were excluded. Results: Age at onset varied from 5-13 years old; 6 were females, all followed from diagnosis up to the last visit (1-10 years). The main features at presentation were recurrent tender parotid swelling and sialectasis imaging, with decreased salivary function assessed by Tc-99 scintigraphy. Mild sicca symptoms were observed in 4/8 cases. Systemic features, including fatigue, myalgia, arthritis, tenosynovitis, joint contractures, transient Raynaud's and high ESR, were recorded at onset. Autoantibody profile was unremarkable for diagnosis, while lymphocytic infiltration of labial salivary glands and sialectasis were observed in all biopsies (8/8). In lachrymal glands, massive lymphocytic infiltration and lymphocytic gastritis were observed during complementary assessment. Flares were treated with low dose steroids and long-term use of hydroxychloroquine (5/8), although only 3/8 fulfilled AECG-2002 diagnostic criteria, throughout the disease course. Conclusion: PPSjS is rare, slowly progressive and its early presentation is variable. Standardised diagnostic algorithms should include recurrent parotid swelling and early diagnosis should rely mostly on salivary and lachrymal gland histopathology in this age group. © Copyright Clinical and Experimental Rheumatology 2011.Department of Paediatrics Botucatu Medical School São Paulo State University (UNESP)Department of Pathology Botucatu Medical School São Paulo State University (UNESP)Department of Paediatrics Botucatu Medical School São Paulo State University (UNESP)Department of Pathology Botucatu Medical School São Paulo State University (UNESP)Universidade Estadual Paulista (UNESP)Saad-Magalhães, Claudia [UNESP]De Souza Medeiros, P. B. [UNESP]Oliveira Sato, J. [UNESP]Custódio Domingues, M. A. [UNESP]2022-04-29T00:13:44Z2022-04-29T00:13:44Z2011-09-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article589-593Clinical and Experimental Rheumatology, v. 29, n. 3, p. 589-593, 2011.0392-856X1593-098Xhttp://hdl.handle.net/11449/2264892-s2.0-80052061607Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengClinical and Experimental Rheumatologyinfo:eu-repo/semantics/openAccess2024-09-03T13:46:21Zoai:repositorio.unesp.br:11449/226489Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T13:46:21Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Clinical presentation and salivary gland histopathology of paediatric primary Sjögren's syndrome
title Clinical presentation and salivary gland histopathology of paediatric primary Sjögren's syndrome
spellingShingle Clinical presentation and salivary gland histopathology of paediatric primary Sjögren's syndrome
Saad-Magalhães, Claudia [UNESP]
Children
Focal sialadenitis
Recurrent parotitis
Sialectasis
Sjögren's syndrome
title_short Clinical presentation and salivary gland histopathology of paediatric primary Sjögren's syndrome
title_full Clinical presentation and salivary gland histopathology of paediatric primary Sjögren's syndrome
title_fullStr Clinical presentation and salivary gland histopathology of paediatric primary Sjögren's syndrome
title_full_unstemmed Clinical presentation and salivary gland histopathology of paediatric primary Sjögren's syndrome
title_sort Clinical presentation and salivary gland histopathology of paediatric primary Sjögren's syndrome
author Saad-Magalhães, Claudia [UNESP]
author_facet Saad-Magalhães, Claudia [UNESP]
De Souza Medeiros, P. B. [UNESP]
Oliveira Sato, J. [UNESP]
Custódio Domingues, M. A. [UNESP]
author_role author
author2 De Souza Medeiros, P. B. [UNESP]
Oliveira Sato, J. [UNESP]
Custódio Domingues, M. A. [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Saad-Magalhães, Claudia [UNESP]
De Souza Medeiros, P. B. [UNESP]
Oliveira Sato, J. [UNESP]
Custódio Domingues, M. A. [UNESP]
dc.subject.por.fl_str_mv Children
Focal sialadenitis
Recurrent parotitis
Sialectasis
Sjögren's syndrome
topic Children
Focal sialadenitis
Recurrent parotitis
Sialectasis
Sjögren's syndrome
description Objective: Explore the presentation, diagnostic criteria and exocrine gland histopathology of paediatric primary Sjögren's syndrome (PPSjS). Methods: A case series of 8 children is reported and American-European Consensus Group (AECG-2002) criteria were examined, as well as minor labial salivary and lachrymal gland biopsies, which were scored by a pathologist blinded to outcome. For all cases, connective tissue diseases and parotid-related infectious disease were excluded. Results: Age at onset varied from 5-13 years old; 6 were females, all followed from diagnosis up to the last visit (1-10 years). The main features at presentation were recurrent tender parotid swelling and sialectasis imaging, with decreased salivary function assessed by Tc-99 scintigraphy. Mild sicca symptoms were observed in 4/8 cases. Systemic features, including fatigue, myalgia, arthritis, tenosynovitis, joint contractures, transient Raynaud's and high ESR, were recorded at onset. Autoantibody profile was unremarkable for diagnosis, while lymphocytic infiltration of labial salivary glands and sialectasis were observed in all biopsies (8/8). In lachrymal glands, massive lymphocytic infiltration and lymphocytic gastritis were observed during complementary assessment. Flares were treated with low dose steroids and long-term use of hydroxychloroquine (5/8), although only 3/8 fulfilled AECG-2002 diagnostic criteria, throughout the disease course. Conclusion: PPSjS is rare, slowly progressive and its early presentation is variable. Standardised diagnostic algorithms should include recurrent parotid swelling and early diagnosis should rely mostly on salivary and lachrymal gland histopathology in this age group. © Copyright Clinical and Experimental Rheumatology 2011.
publishDate 2011
dc.date.none.fl_str_mv 2011-09-15
2022-04-29T00:13:44Z
2022-04-29T00:13:44Z
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 Clinical and Experimental Rheumatology, v. 29, n. 3, p. 589-593, 2011.
0392-856X
1593-098X
http://hdl.handle.net/11449/226489
2-s2.0-80052061607
identifier_str_mv Clinical and Experimental Rheumatology, v. 29, n. 3, p. 589-593, 2011.
0392-856X
1593-098X
2-s2.0-80052061607
url http://hdl.handle.net/11449/226489
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Clinical and Experimental Rheumatology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 589-593
dc.source.none.fl_str_mv Scopus
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)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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