Multierosive Juvenile Idiopathic Arthritis With Positive Rheumatoid Factor: A Case Report of a Young Girl Followed at the University Clinics of Bukavu.

Case Reports in Rheumatology Pub Date : 2026-07-26 eCollection Date: 2026-01-01 DOI:10.1155/crrh/9884531
Delphin Murhula Katabana, Théophile Barhwamire Kabesha, Rodrigue Mupenda Mwenibamba, Roland Lwandiko Cibenda, Paul Ngongo Tshonda, Archippe Birindwa Muhandule, Philippe Katchunga Bianga, Tony Shindano Akilimali
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Abstract

Polyarticular juvenile idiopathic arthritis (JIA) with positive rheumatoid factor is a rare and severe form of chronic inflammatory rheumatism in children. We report the case of a young girl treated at the University Clinics of Bukavu (eastern DR Congo), whose disease began at the age of 10. The course of the disease was characterized by highly inflammatory polyarthritis with severe multierosive lesions. Immunological testing revealed positivity for rheumatoid factor and anti-CCP antibodies. Diagnosis and treatment were delayed for approximately nine years (2008-2017). Management was complicated by poor adherence and discontinuation of methotrexate and corticosteroids. The patient subsequently died to recurrent infectious complications and hypertension. This case illustrates the impact of diagnostic delay and difficulties in accessing care on the prognosis of severe forms of JIA in resource-limited settings.

多糜糜性幼年特发性关节炎伴类风湿因子阳性:一例在布卡武大学诊所随访的年轻女孩。
类风湿因子阳性的多关节幼年特发性关节炎(JIA)是一种罕见且严重的儿童慢性炎症性风湿病。我们报告了在布卡武大学诊所(刚果民主共和国东部)治疗的一名年轻女孩的病例,她的疾病始于10岁。病程的特点是高度炎症性多关节炎和严重的多糜烂病变。免疫检查类风湿因子及抗ccp抗体阳性。诊断和治疗延迟了大约9年(2008-2017年)。治疗因依从性差和停止使用甲氨蝶呤和皮质类固醇而变得复杂。患者随后死于复发性感染并发症和高血压。这一病例说明了在资源有限的环境中,诊断延误和难以获得护理对严重形式JIA预后的影响。
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