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Clinical patterns and the evolution of relapsing polychondritis based on organ involvement: a Chinese retrospective cohort study.

Authors :
Zhang, Lei
Yun, Shuang
Wu, Tiange
He, Yujie
Guo, Jinyan
Han, Lishuai
Lu, Jiameng
Liu, Xiaojun
Yang, Rui
Zhang, Shitao
Li, Tianfang
Liu, Shengyun
Source :
Orphanet Journal of Rare Diseases. 5/17/2021, Vol. 16 Issue 1, p1-11. 11p.
Publication Year :
2021

Abstract

<bold>Background: </bold>Relapsing polychondritis (RPC) is a rare autoimmune disease and its early diagnosis remains challenging. Defining the clinical patterns and disease course may help early recognition of RPC.<bold>Results: </bold>Sixty-six males and 60 females were included in this study. The average age at onset were 47.1 ± 13.8 years and the median follow-up period was 18 months. Correlation analysis revealed a strong negative correlation between airway involvement and auricular chondritis (r = - 0.75, P < 0.001). Four distinct clinical patterns were identified: Ear pattern (50.8%), Airway pattern (38.9%), Overlap pattern (4.8%) and Airway-Ear negative pattern (5.6%), and patients with Ear pattern and Airway pattern were further divided into limited and systemic form of RPC (27.8% with limited form of Ear pattern and 24.6% with limited form of Airway pattern initially). During follow-up, a minority of patients with Ear pattern and Airway pattern progressed into Overlap pattern, and some Airway-Ear negative pattern patients progressed into Ear pattern. While a large majority of limited RPC patients remained limited form during follow-up, a minority of limited RPC patients progressed into systemic form. Patients with Ear pattern had the highest survival rate and relatively lower inflammatory status.<bold>Conclusions: </bold>RPC patients can be categorized as 4 different clinical patterns and 2 distinct presenting forms (limited and systemic) based on organ involvement. The clinical patterns and presenting forms may evolve during follow-up. Our findings may facilitate early recognition of this rare disease. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17501172
Volume :
16
Issue :
1
Database :
Academic Search Index
Journal :
Orphanet Journal of Rare Diseases
Publication Type :
Academic Journal
Accession number :
150341964
Full Text :
https://doi.org/10.1186/s13023-021-01861-x