Clinical presentation and salivary gland histopathology of paediatric primary Sjögren's syndrome
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , |
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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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 |
_version_ |
1826303678316806144 |