Progressive systemic sclerosis and acute interstitial lung disease in children: a case report

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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...

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Detalles Bibliográficos
Autor: Núñez Moscoso, Luis Enrique
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
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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
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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
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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)
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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
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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
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