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

被引:7
作者
Pannu, Ashok Kumar [1 ]
Singla, Vidhi [1 ]
Suri, Vikas [1 ]
Kumar, Rajender [2 ]
Mathur, Yamini [2 ]
Mohindra, Ritin [1 ]
Jain, Sanjay [1 ]
机构
[1] Postgrad Inst Med Educ & Res, Nehru Hosp, Dept Internal Med, Sect 12,4th Floor,F Block, Chandigarh 160012, India
[2] Postgrad Inst Med Educ & Res, Nehru Hosp, Dept Nucl Med, Sect 12, Chandigarh 160012, India
关键词
Fever of unknown origin; Pyrexia of unknown origin; Adult-onset Still's disease; Adults; Macrophage activation syndrome; Diagnosis; India; CLASSIFICATION CRITERIA; DIAGNOSIS;
D O I
10.1007/s10238-022-00903-3
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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 degrees 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.
引用
收藏
页码:1659 / 1666
页数:8
相关论文
共 30 条
[1]   Pyrexia of unknown origin in HIV-negative adults from Himachal Pradesh (India): will you suspect disseminated histoplasmosis? [J].
Arora, Navneet ;
Shukla, Shubham ;
Vijaykumar, Deeksha ;
Suri, Vikas ;
Kumar, Rajender ;
Pannu, Ashok K. .
TROPICAL DOCTOR, 2020, 50 (03) :275-277
[2]   Rheumatic disorders among patients with fever of unknown origin: A systematic review and meta-analysis [J].
Betrains, A. ;
Moreel, L. ;
De Langhe, E. ;
Blockmans, D. ;
Vanderschueren, S. .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 2022, 56
[3]   Retrospective study of 61 patients with adult-onset Still's disease admitted with fever of unknown origin in China [J].
Chen, Pei-Dong ;
Yu, Sheng-Lei ;
Chen, Shu ;
Weng, Xin-Hua .
CLINICAL RHEUMATOLOGY, 2012, 31 (01) :175-181
[4]   Adult-onset still disease as the cause of fever of unknown origin [J].
Crispín, JC ;
Martínez-Baños, D ;
Alcocer-Varela, J .
MEDICINE, 2005, 84 (06) :331-337
[5]   18F-FDG PET/CT in patients with adult-onset Still's disease [J].
Dong, Meng-Jie ;
Wang, Cai-qin ;
Zhao, Kui ;
Wang, Guo-Lin ;
Sun, Mei-Ling ;
Liu, Zhen-Feng ;
Xu, Liqin .
CLINICAL RHEUMATOLOGY, 2015, 34 (12) :2047-2056
[6]   Adult-onset Still's disease in focus: Clinical manifestations, diagnosis, treatment, and unmet needs in the era of targeted therapies [J].
Efthimiou, Petros ;
Kontzias, Apostolos ;
Hur, Peter ;
Rodha, Kavita ;
Ramakrishna, G. S. ;
Nakasato, Priscila .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 2021, 51 (04) :858-874
[7]  
Ekbote GS, 2018, INDIAN J RHEUMATOL, V13, pS185
[8]   Development and Validation of the HScore, a Score for the Diagnosis of Reactive Hemophagocytic Syndrome [J].
Fardet, Laurence ;
Galicier, Lionel ;
Lambotte, Olivier ;
Marzac, Christophe ;
Aumont, Cedric ;
Chahwan, Doumit ;
Coppo, Paul ;
Hejblum, Gilles .
ARTHRITIS & RHEUMATOLOGY, 2014, 66 (09) :2613-2620
[9]   Proposal for a new set of classification criteria for adult-onset Still disease [J].
Fautrel, B ;
Zing, E ;
Golmard, JL ;
Le Moel, G ;
Bissery, A ;
Rioux, C ;
Rozenberg, S ;
Piette, JC ;
Bourgeois, P .
MEDICINE, 2002, 81 (03) :194-200
[10]   Multisystem Inflammatory Syndrome in US Children and Adolescents [J].
Feldstein, Leora R. ;
Rose, Erica B. ;
Horwitz, Steven M. ;
Collins, Jennifer P. ;
Newhams, Margaret M. ;
Son, Mary Beth F. ;
Newburger, Jane W. ;
Kleinman, Lawrence C. ;
Heidemann, Sabrina M. ;
Martin, Amarilis A. ;
Singh, Aalok R. ;
Li, Simon ;
Tarquinio, Keiko M. ;
Jaggi, Preeti ;
Oster, Matthew E. ;
Zackai, Sheemon P. ;
Gillen, Jennifer ;
Ratner, Adam J. ;
Walsh, Rowan F. ;
Fitzgerald, Julie C. ;
Keenaghan, Michael A. ;
Alharash, Hussam ;
Doymaz, Sule ;
Clouser, Katharine N. ;
Giuliano, John S. ;
Gupta, Anjali ;
Parker, Robert M. ;
Maddux, Aline B. ;
Havalad, Vinod ;
Ramsingh, Stacy ;
Bukulmez, Hulya ;
Bradford, Tamara T. ;
Smith, Lincoln S. ;
Tenforde, Mark W. ;
Carroll, Christopher L. ;
Riggs, Becky J. ;
Gertz, Shira J. ;
Daube, Ariel ;
Lansell, Amanda ;
Coronado Munoz, Alvaro ;
Hobbs, Charlotte V. ;
Marohn, Kimberly L. ;
Halasa, Natasha B. ;
Patel, Manish M. ;
Randolph, Adrienne G. .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 383 (04) :334-346