Bilateral Knee Synovial Chondromatosis in a 2-Year-Old Girl: First Reported Case and Literature Review.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Ana Paula Fernandes Barbosa, Paulyana Fernandes Barbosa Quintino, Hermann Fernandes Motta Camara, Pedro Henrique Laurindo Dos Anjos, Arthur Castro Guimaraes, Eloisio Barbosa Lopes Neto, Maria Eugenia Leite Duarte
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Abstract

BACKGROUND Synovial chondromatosis (SC) is a rare monoarticular benign condition characterized by the development of intra- or periarticular cartilage-like nodules or loose bodies. Typically affecting middle-aged men, SC is exceptionally rare in female pediatric patients. Symptoms include diffuse pain, swelling, and limited joint movement. The loose bodies are typically numerous, small, rounded, and uniform in size. Histologically, they consist of hyaline cartilage-like nodules containing clusters of chondrocytes. Bilateral SC in the knee of young children is even rarer and has not been previously documented in the medical literature. CASE REPORT A 2-year-old girl presented with recent pain in her right knee without preceding trauma. Physical examination revealed joint effusion, a limping gait, and limited knee flexion, with no signs of local inflammation. Radiographs showed normal joint structures, and laboratory test results, except for an elevated CRP, were normal. Joint aspiration ruled out septic arthritis. The worsening of symptoms within a relatively short period prompted further investigation, leading to the identification of numerous cartilaginous nodules within the joint during exploratory arthrotomy. Microscopic examination revealed unossified cartilage-like nodules containing disorganized chondrocytes. Four months after surgery, she was diagnosed with SC in the contralateral knee. CONCLUSIONS Given the rarity of synovial chondromatosis in young children, and the even rarer bilateral presentation in a large joint, this case report provides an opportunity to explore the challenges in diagnosing and managing such conditions in pediatric patients. To the best of our knowledge, this is the youngest reported case of bilateral SC of the knee in a pediatric patient.

1例2岁女童双侧膝关节滑膜软骨瘤病:首次报道并文献复习。
滑膜软骨瘤病(SC)是一种罕见的单关节良性疾病,其特征是关节内或关节周围软骨样结节或松散体的发展。SC通常影响中年男性,在女性儿科患者中极为罕见。症状包括弥漫性疼痛、肿胀和关节活动受限。松散体通常数量多、小、圆、大小均匀。组织学上,它们由透明的软骨样结节组成,结节中含有软骨细胞簇。幼儿双侧膝关节SC更为罕见,以前在医学文献中没有记录。病例报告一名2岁女童,近期无外伤,右膝疼痛。体格检查显示关节积液,步态跛行,膝关节屈曲有限,无局部炎症征象。x线片显示关节结构正常,实验室检查结果除CRP升高外均正常。关节穿刺排除了脓毒性关节炎。在相对较短的时间内症状恶化促使进一步调查,导致在探查性关节切开术中发现关节内许多软骨结节。镜下检查显示未硬化的软骨样结节,包含无组织的软骨细胞。术后4个月,她被诊断为对侧膝关节SC。结论:考虑到滑膜软骨瘤病在幼儿中的罕见性,以及在大关节中更罕见的双侧表现,本病例报告为探讨儿科患者诊断和治疗此类疾病的挑战提供了机会。据我们所知,这是最年轻的报告病例双侧膝关节SC的儿科患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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