Childhood-Onset COPA Syndrome Recognized Retrospectively in the Context of Polyarticular Juvenile Idiopathic Arthritis and Rheumatoid Arthritis.

Roko P A Nikolic, Cristina Moran Toro
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Abstract

COPA syndrome is a very rare autoinflammatory disorder manifesting with childhood-onset arthritis and pulmonary and renal disease, of which awareness may remain lacking. We present the case of a twenty-year-old male patient seen in the Young Adults with Rheumatic Disease clinic. Initially diagnosed with seropositive polyarticular juvenile idiopathic arthritis, the patient's early childhood complaints of fatiguability, paroxysmal dyspnea, and pneumonia-like episodes were long to be felt unrelated to his arthritis. Upon transition to adult rheumatology care, a thorough review of the patient's history prompted imaging which revealed interstitial lung disease. Restrictive spirometry and genetic testing confirmed the retrospective diagnosis of COPA syndrome.

Abstract Image

儿童期发作的COPA综合征在多关节幼年特发性关节炎和类风湿关节炎的背景下回顾性识别。
COPA综合征是一种非常罕见的自身炎症性疾病,表现为儿童期发病的关节炎、肺部和肾脏疾病,对这种疾病的认识可能仍然缺乏。我们提出的情况下,一个二十岁的男性患者看到的年轻成人风湿病诊所。最初诊断为血清阳性多关节幼年特发性关节炎,患者童年早期的疲劳、阵发性呼吸困难和肺炎样发作,长期被认为与他的关节炎无关。在过渡到成人风湿病护理,彻底检讨病人的历史提示影像学显示间质性肺疾病。限制性肺活量测定和基因检测证实回顾性诊断为COPA综合征。
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