Navicular avascular necrosis in juvenile idiopathic arthritis.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Vaibhav S Bellary, Jitendra Shankarlal Oswal, Deepti Agarwal, Nikhila B Kadimisetty
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引用次数: 0

Abstract

We present a case of a child in middle childhood (6-11 years) diagnosed with juvenile idiopathic arthritis (JIA) who developed glucocorticoid-induced avascular necrosis (AVN) of the navicular bone. Glucocorticoid-induced AVN in children, particularly of the navicular bone, is a rare but serious complication. Glucocorticoid therapy, often used in managing JIA, can disrupt the blood supply to developing bones, leading to AVN. Early recognition and intervention are crucial to prevent long-term morbidity. This case underscores the importance of minimising the duration of prolonged glucocorticoid use in children.

幼年特发性关节炎的舟骨缺血性坏死。
我们报告了一个儿童在儿童中期(6-11岁)诊断为青少年特发性关节炎(JIA)发展为糖皮质激素诱导的舟骨缺血性坏死(AVN)的病例。糖皮质激素引起的儿童AVN,特别是舟骨,是一种罕见但严重的并发症。糖皮质激素治疗通常用于治疗JIA,可破坏正在发育的骨骼的血液供应,导致AVN。早期识别和干预对于预防长期发病至关重要。本病例强调了尽量减少儿童长期使用糖皮质激素的时间的重要性。
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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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