Progressive systemic sclerosis and acute interstitial lung disease in children: a case report
Descripción del Articulo
Childhood or juvenile scleroderma is the third most common pediatric chronic rheumatic diseasefollowing juvenile idiopathic arthritis (JIA) and systemic lupus erythematosus (SLE). It has twomain forms: systemic and localized. The available information remains very limited, as few serieshave been pub...
Autor: | |
---|---|
Formato: | artículo |
Fecha de Publicación: | 2025 |
Institución: | Universidad de San Martín de Porres |
Repositorio: | Horizonte médico |
Lenguaje: | español |
OAI Identifier: | oai:horizontemedico.usmp.edu.pe:article/3037 |
Enlace del recurso: | https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/3037 |
Nivel de acceso: | acceso abierto |
Materia: | Esclerosis Sintémica Enfermedad Pulmonar Intersticial Juvenil Systemic Sclerosis ; Lung Diseases, Interstitial Juvenile |
id |
REVHM_e1c93d9a82116640e9aa743323860a9a |
---|---|
oai_identifier_str |
oai:horizontemedico.usmp.edu.pe:article/3037 |
network_acronym_str |
REVHM |
network_name_str |
Horizonte médico |
repository_id_str |
|
dc.title.none.fl_str_mv |
Progressive systemic sclerosis and acute interstitial lung disease in children: a case report Esclerosis sistémica progresiva y enfermedad intersticial pulmonar aguda en niños: a propósito de un caso |
title |
Progressive systemic sclerosis and acute interstitial lung disease in children: a case report |
spellingShingle |
Progressive systemic sclerosis and acute interstitial lung disease in children: a case report Núñez Moscoso, Luis Enrique Esclerosis Sintémica Enfermedad Pulmonar Intersticial Juvenil Systemic Sclerosis ; Lung Diseases, Interstitial Juvenile |
title_short |
Progressive systemic sclerosis and acute interstitial lung disease in children: a case report |
title_full |
Progressive systemic sclerosis and acute interstitial lung disease in children: a case report |
title_fullStr |
Progressive systemic sclerosis and acute interstitial lung disease in children: a case report |
title_full_unstemmed |
Progressive systemic sclerosis and acute interstitial lung disease in children: a case report |
title_sort |
Progressive systemic sclerosis and acute interstitial lung disease in children: a case report |
dc.creator.none.fl_str_mv |
Núñez Moscoso, Luis Enrique |
author |
Núñez Moscoso, Luis Enrique |
author_facet |
Núñez Moscoso, Luis Enrique |
author_role |
author |
dc.subject.none.fl_str_mv |
Esclerosis Sintémica Enfermedad Pulmonar Intersticial Juvenil Systemic Sclerosis ; Lung Diseases, Interstitial Juvenile |
topic |
Esclerosis Sintémica Enfermedad Pulmonar Intersticial Juvenil Systemic Sclerosis ; Lung Diseases, Interstitial Juvenile |
description |
Childhood or juvenile scleroderma is the third most common pediatric chronic rheumatic diseasefollowing juvenile idiopathic arthritis (JIA) and systemic lupus erythematosus (SLE). It has twomain forms: systemic and localized. The available information remains very limited, as few serieshave been published, and most of them include a small number of patients. On the other hand,the classification and management of the disease have evolved over time.The diagnosis of interstitial lung diseases (ILDs) in adults—and even more so in children—constitutes a significant challenge for clinicians. ILDs of inflammatory origin are rare in adultsand can be considered almost exceptional in children; the largest series report no more than 50cases. Autoimmune forms of IDLs in children represent a particularly complex category, as theyinvolve aberrant immunological mechanisms that affect both the lungs and other organs. This cancomplicate diagnosis and treatment, and may worsen the prognosis.The relationship between systemic sclerosis in children and acute ILD is complex and remainsunder investigation. Early diagnosis, clinical assessment and appropriate treatment are essentialto improve the prognosis and quality of life of affected pediatric patients. Given the particularrelevance of both diseases and the limited information available in the literature, we present thecase of a 6-year-old patient in whom both occurred at different stages of disease. |
publishDate |
2025 |
dc.date.none.fl_str_mv |
2025-06-28 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/3037 10.24265/horizmed.2025.v25n2.16 |
url |
https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/3037 |
identifier_str_mv |
10.24265/horizmed.2025.v25n2.16 |
dc.language.none.fl_str_mv |
spa |
language |
spa |
dc.relation.none.fl_str_mv |
https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/3037/2230 https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/3037/2265 https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/3037/2313 |
dc.rights.none.fl_str_mv |
Derechos de autor 1970 Horizonte Médico (Lima) https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Derechos de autor 1970 Horizonte Médico (Lima) https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf text/xml text/html |
dc.publisher.none.fl_str_mv |
Universidad de San Martín de Porres. Facultad de Medicina Humana |
publisher.none.fl_str_mv |
Universidad de San Martín de Porres. Facultad de Medicina Humana |
dc.source.none.fl_str_mv |
Horizonte Médico (Lima); Vol. 25 No. 2 (2025): Abril-Junio; e3037 Horizonte Médico (Lima); Vol. 25 Núm. 2 (2025): Abril-Junio; e3037 Horizonte Médico (Lima); v. 25 n. 2 (2025): Abril-Junio; e3037 2227-3530 1727-558X reponame:Horizonte médico instname:Universidad de San Martín de Porres instacron:USMP |
instname_str |
Universidad de San Martín de Porres |
instacron_str |
USMP |
institution |
USMP |
reponame_str |
Horizonte médico |
collection |
Horizonte médico |
repository.name.fl_str_mv |
|
repository.mail.fl_str_mv |
|
_version_ |
1844720563906412544 |
spelling |
Progressive systemic sclerosis and acute interstitial lung disease in children: a case reportEsclerosis sistémica progresiva y enfermedad intersticial pulmonar aguda en niños: a propósito de un casoNúñez Moscoso, Luis EnriqueEsclerosis SintémicaEnfermedad Pulmonar IntersticialJuvenilSystemic Sclerosis; Lung Diseases, InterstitialJuvenileChildhood or juvenile scleroderma is the third most common pediatric chronic rheumatic diseasefollowing juvenile idiopathic arthritis (JIA) and systemic lupus erythematosus (SLE). It has twomain forms: systemic and localized. The available information remains very limited, as few serieshave been published, and most of them include a small number of patients. On the other hand,the classification and management of the disease have evolved over time.The diagnosis of interstitial lung diseases (ILDs) in adults—and even more so in children—constitutes a significant challenge for clinicians. ILDs of inflammatory origin are rare in adultsand can be considered almost exceptional in children; the largest series report no more than 50cases. Autoimmune forms of IDLs in children represent a particularly complex category, as theyinvolve aberrant immunological mechanisms that affect both the lungs and other organs. This cancomplicate diagnosis and treatment, and may worsen the prognosis.The relationship between systemic sclerosis in children and acute ILD is complex and remainsunder investigation. Early diagnosis, clinical assessment and appropriate treatment are essentialto improve the prognosis and quality of life of affected pediatric patients. Given the particularrelevance of both diseases and the limited information available in the literature, we present thecase of a 6-year-old patient in whom both occurred at different stages of disease.La esclerodermia infantil o juvenil representa la tercera enfermedad reumática crónica infantil en frecuencia tras la artritis idiopática juvenil (AIJ) y el lupus eritematoso sistémico (LES). Sus dos principales grupos son las formas sistémica y localizada. La información existente es muy limitada, ya que no son muchas las series publicadas y, salvo algunas, consideran pocos pacientes; por otro lado, ha evolucionado en su clasificación y manejo. El diagnóstico de las enfermedades pulmonares intersticiales (EPI) en adultos, y más aún en la infancia, constituye un verdadero reto para el clínico. Las EPI de origen inflamatorio son poco frecuentes en adultos y pueden considerarse casi excepcionales en niños, pues las series más amplias no superan el medio centenar. Las formas autoinmunes de EPI en niños representan unacategoría particularmente compleja, ya que involucran mecanismos inmunológicos aberrantes que afectan tanto los pulmones como otros órganos, lo que puede dificultar el diagnóstico y tratamiento, además de ensombrecer el pronóstico. La relación entre la esclerosis sistémica en niños y la EPI aguda es compleja y aún está siendo investigada. El diagnóstico temprano, la evaluación clínica y el tratamiento adecuado son esenciales para mejorar el pronóstico y la calidad de vida de los pacientes pediátricos afectados. Siendo ambas de interés particular y teniendo en consideración la escasa información documentada, se presenta un paciente de seis años en quien ambas condiciones aparecen en diferentes momentos de la enfermedad.Universidad de San Martín de Porres. Facultad de Medicina Humana2025-06-28info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdftext/xmltext/htmlhttps://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/303710.24265/horizmed.2025.v25n2.16Horizonte Médico (Lima); Vol. 25 No. 2 (2025): Abril-Junio; e3037Horizonte Médico (Lima); Vol. 25 Núm. 2 (2025): Abril-Junio; e3037Horizonte Médico (Lima); v. 25 n. 2 (2025): Abril-Junio; e30372227-35301727-558Xreponame:Horizonte médicoinstname:Universidad de San Martín de Porresinstacron:USMPspahttps://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/3037/2230https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/3037/2265https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/3037/2313Derechos de autor 1970 Horizonte Médico (Lima)https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessoai:horizontemedico.usmp.edu.pe:article/30372025-06-28T19:53:36Z |
score |
13.4165325 |
Nota importante:
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).