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Adult-onset Still’s disease and fever of unknown origin in India

Despite an essential differential diagnosis for fever of unknown origin (FUO) in young adults, adult-onset Still’s disease (AOSD) is infrequently considered and remained underdiagnosed in low-middle-income countries. The present study analyzed the clinical, serological, radiological, and pathologica...

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Autores principales: Pannu, Ashok Kumar, Singla, Vidhi, Suri, Vikas, Kumar, Rajender, Mathur, Yamini, Mohindra, Ritin, Jain, Sanjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9523624/
https://www.ncbi.nlm.nih.gov/pubmed/36178600
http://dx.doi.org/10.1007/s10238-022-00903-3
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author Pannu, Ashok Kumar
Singla, Vidhi
Suri, Vikas
Kumar, Rajender
Mathur, Yamini
Mohindra, Ritin
Jain, Sanjay
author_facet Pannu, Ashok Kumar
Singla, Vidhi
Suri, Vikas
Kumar, Rajender
Mathur, Yamini
Mohindra, Ritin
Jain, Sanjay
author_sort Pannu, Ashok Kumar
collection PubMed
description Despite an essential differential diagnosis for fever of unknown origin (FUO) in young adults, adult-onset Still’s disease (AOSD) is infrequently considered and remained underdiagnosed in low-middle-income countries. The present study analyzed the clinical, serological, radiological, and pathological characteristics of AOSD presented as FUO in India. A hospital-based retrospective study of patients aged > 13 years admitted with FUO and later diagnosed with AOSD in Postgraduate Institute of Medical Education and Research, Chandigarh (India), was conducted between January 2014 and December 2020. Petersdorf and Beeson’s criteria were used to define FUO. The diagnosis of AOSD was made based on Yamaguchi’s criteria. Twenty-seven patients (median age 26 years, 14 females) were enrolled. All presented with intermittent fever with a median duration of 10 weeks. The typical features of AOSD at admission were arthralgia (n = 24), hepatosplenomegaly (n = 21), spiking fever ≥ 39 °C (n = 19), lymphadenopathy (n = 18), typical rash (n = 17), and sore throat (n = 11). Leukocytosis (n = 25) and neutrophilia (n = 19) were frequent. Hyperferritinemia was universal (range, 700–145,003 ng/ml; ≥ 2000, n = 23). At admission, AOSD was suspected in only nine FUO cases, while tuberculosis (n = 16), undifferentiated connective tissue disorder (n = 14), and lymphoproliferative disorder (n = 11) were common diagnostic possibilities. Crispin et al. clinical scale detected AOSD in only 15 (55.5%) FUO patients. Whole-body imaging (n = 27), including fluorodeoxyglucose positron emission tomography (n = 12), demonstrated reticuloendothelial organ-system involvement and serositis. Seventeen (63%) patients had macrophage activation syndrome at the time of AOSD diagnosis. AOSD FUO presents with typical but nonspecific features; thus, early differentiation from common causes (e.g., tuberculosis, lymphoma) is difficult. Macrophage activation syndrome is common in AOSD with FUO presentation.
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spelling pubmed-95236242022-09-30 Adult-onset Still’s disease and fever of unknown origin in India Pannu, Ashok Kumar Singla, Vidhi Suri, Vikas Kumar, Rajender Mathur, Yamini Mohindra, Ritin Jain, Sanjay Clin Exp Med Original Article Despite an essential differential diagnosis for fever of unknown origin (FUO) in young adults, adult-onset Still’s disease (AOSD) is infrequently considered and remained underdiagnosed in low-middle-income countries. The present study analyzed the clinical, serological, radiological, and pathological characteristics of AOSD presented as FUO in India. A hospital-based retrospective study of patients aged > 13 years admitted with FUO and later diagnosed with AOSD in Postgraduate Institute of Medical Education and Research, Chandigarh (India), was conducted between January 2014 and December 2020. Petersdorf and Beeson’s criteria were used to define FUO. The diagnosis of AOSD was made based on Yamaguchi’s criteria. Twenty-seven patients (median age 26 years, 14 females) were enrolled. All presented with intermittent fever with a median duration of 10 weeks. The typical features of AOSD at admission were arthralgia (n = 24), hepatosplenomegaly (n = 21), spiking fever ≥ 39 °C (n = 19), lymphadenopathy (n = 18), typical rash (n = 17), and sore throat (n = 11). Leukocytosis (n = 25) and neutrophilia (n = 19) were frequent. Hyperferritinemia was universal (range, 700–145,003 ng/ml; ≥ 2000, n = 23). At admission, AOSD was suspected in only nine FUO cases, while tuberculosis (n = 16), undifferentiated connective tissue disorder (n = 14), and lymphoproliferative disorder (n = 11) were common diagnostic possibilities. Crispin et al. clinical scale detected AOSD in only 15 (55.5%) FUO patients. Whole-body imaging (n = 27), including fluorodeoxyglucose positron emission tomography (n = 12), demonstrated reticuloendothelial organ-system involvement and serositis. Seventeen (63%) patients had macrophage activation syndrome at the time of AOSD diagnosis. AOSD FUO presents with typical but nonspecific features; thus, early differentiation from common causes (e.g., tuberculosis, lymphoma) is difficult. Macrophage activation syndrome is common in AOSD with FUO presentation. Springer International Publishing 2022-09-30 /pmc/articles/PMC9523624/ /pubmed/36178600 http://dx.doi.org/10.1007/s10238-022-00903-3 Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Pannu, Ashok Kumar
Singla, Vidhi
Suri, Vikas
Kumar, Rajender
Mathur, Yamini
Mohindra, Ritin
Jain, Sanjay
Adult-onset Still’s disease and fever of unknown origin in India
title Adult-onset Still’s disease and fever of unknown origin in India
title_full Adult-onset Still’s disease and fever of unknown origin in India
title_fullStr Adult-onset Still’s disease and fever of unknown origin in India
title_full_unstemmed Adult-onset Still’s disease and fever of unknown origin in India
title_short Adult-onset Still’s disease and fever of unknown origin in India
title_sort adult-onset still’s disease and fever of unknown origin in india
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9523624/
https://www.ncbi.nlm.nih.gov/pubmed/36178600
http://dx.doi.org/10.1007/s10238-022-00903-3
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