Juvenile Idiopathic Arthritis Onset in a Neonate: A Rare Case Report

Background: A common type of chronic arthritis in children and adolescents is juvenile idiopathic arthritis (JIA).According to the International League of Associations for Rheumatology (ILAR) classification, JIA diagnostic criteria include age under 16 years and disease duration of six-weeks. Based...

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Main Authors: Abdolreza Malek, Mohammad-Saeed Sasan, Narges Afzali, Somayeh Ghahremani, Sara Ghahremani
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2017-06-01
Series:Iranian Journal of Neonatology
Subjects:
Online Access:http://ijn.mums.ac.ir/article_8923_5017adafb2476c70dc01bd05e6e8db86.pdf
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author Abdolreza Malek
Mohammad-Saeed Sasan
Narges Afzali
Somayeh Ghahremani
Sara Ghahremani
author_facet Abdolreza Malek
Mohammad-Saeed Sasan
Narges Afzali
Somayeh Ghahremani
Sara Ghahremani
author_sort Abdolreza Malek
collection DOAJ
description Background: A common type of chronic arthritis in children and adolescents is juvenile idiopathic arthritis (JIA).According to the International League of Associations for Rheumatology (ILAR) classification, JIA diagnostic criteria include age under 16 years and disease duration of six-weeks. Based on the number of involved joints in the first sixmonths of disease onset, JIA is categorized into oligoarticular or polyarticular subtypes. Age is a characteristic factor in the diagnosis of disease subsets; it is worth mentioning that cases younger than six months of age are seldom found in any of the subtypes. Case report: In this report, we present a rare case of JIA in an infant, presenting at 20 days of age. Effusion of the right hip joint was one of the primary manifestations of the disease. During hospitalization, she went through sepsis workup and a four-week antibiotic therapy for management of lower limb pseudoparalysis. In spite of antibiotic therapy, she developed effusion of a second joint. According to the course and duration of symptoms and ILAR classification forJIA, oligoarticular JIA was diagnosed and treated.Conclusion: In this case, infectious diseases, such as tuberculosis and brucellosis, and malignancies were ruled out as a cause of inflammation through bone marrow aspiration, culture, and tests; ultrasound and magnetic resonance imaging showed no lytic and sclerotic lesions or a fracture. Our experience showed a rare case of JIA and suggested that JIA must be considered in children with joint inflammation at any age
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spelling doaj.art-80effb0f20a0482f8c29742070f076bb2022-12-21T21:56:13ZengMashhad University of Medical SciencesIranian Journal of Neonatology2251-75102322-21582017-06-0182535610.22038/ijn.2017.89238923Juvenile Idiopathic Arthritis Onset in a Neonate: A Rare Case ReportAbdolreza Malek0Mohammad-Saeed Sasan1Narges Afzali2Somayeh Ghahremani3Sara Ghahremani4Department of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, IranDepartment of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, IranDepartment of Radiology, Mashhad Branch, Islamic Azad University, Mashhad, IranNuclear Medicine Research Center, Mashhad University of Medical Sciences, Mashhad, IranDepartment of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, IranBackground: A common type of chronic arthritis in children and adolescents is juvenile idiopathic arthritis (JIA).According to the International League of Associations for Rheumatology (ILAR) classification, JIA diagnostic criteria include age under 16 years and disease duration of six-weeks. Based on the number of involved joints in the first sixmonths of disease onset, JIA is categorized into oligoarticular or polyarticular subtypes. Age is a characteristic factor in the diagnosis of disease subsets; it is worth mentioning that cases younger than six months of age are seldom found in any of the subtypes. Case report: In this report, we present a rare case of JIA in an infant, presenting at 20 days of age. Effusion of the right hip joint was one of the primary manifestations of the disease. During hospitalization, she went through sepsis workup and a four-week antibiotic therapy for management of lower limb pseudoparalysis. In spite of antibiotic therapy, she developed effusion of a second joint. According to the course and duration of symptoms and ILAR classification forJIA, oligoarticular JIA was diagnosed and treated.Conclusion: In this case, infectious diseases, such as tuberculosis and brucellosis, and malignancies were ruled out as a cause of inflammation through bone marrow aspiration, culture, and tests; ultrasound and magnetic resonance imaging showed no lytic and sclerotic lesions or a fracture. Our experience showed a rare case of JIA and suggested that JIA must be considered in children with joint inflammation at any agehttp://ijn.mums.ac.ir/article_8923_5017adafb2476c70dc01bd05e6e8db86.pdfChronic arthritisjuvenile idiopathic arthritisNeonate
spellingShingle Abdolreza Malek
Mohammad-Saeed Sasan
Narges Afzali
Somayeh Ghahremani
Sara Ghahremani
Juvenile Idiopathic Arthritis Onset in a Neonate: A Rare Case Report
Iranian Journal of Neonatology
Chronic arthritis
juvenile idiopathic arthritis
Neonate
title Juvenile Idiopathic Arthritis Onset in a Neonate: A Rare Case Report
title_full Juvenile Idiopathic Arthritis Onset in a Neonate: A Rare Case Report
title_fullStr Juvenile Idiopathic Arthritis Onset in a Neonate: A Rare Case Report
title_full_unstemmed Juvenile Idiopathic Arthritis Onset in a Neonate: A Rare Case Report
title_short Juvenile Idiopathic Arthritis Onset in a Neonate: A Rare Case Report
title_sort juvenile idiopathic arthritis onset in a neonate a rare case report
topic Chronic arthritis
juvenile idiopathic arthritis
Neonate
url http://ijn.mums.ac.ir/article_8923_5017adafb2476c70dc01bd05e6e8db86.pdf
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AT somayehghahremani juvenileidiopathicarthritisonsetinaneonateararecasereport
AT saraghahremani juvenileidiopathicarthritisonsetinaneonateararecasereport