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儿童踝关节原发性滑膜软骨瘤病:1例罕见病例报告及文献复习

Primary Synovial Chondromatosis of the Ankle in a Child: A Rare Case Presentation and Review of Literature.

作者信息

Yadav Sandeep K, Rajnish Rajesh K, Kumar Dhirendra, Khera Sudeep, Elhence Abhay, Choudhary Aakash

机构信息

Department of Orthopedics, AIIMS, Jodhpur, Rajasthan, India.

Department of Pathology, AIIMS Jodhpur, Rajasthan, India.

出版信息

J Orthop Case Rep. 2023 Apr;13(4):5-10. doi: 10.13107/jocr.2023.v13.i04.3594.

Abstract

INTRODUCTION

Synovial chondromatosis is not a common condition and involvement of the ankle joint is quite rare. We found only one case of synovial chondromatosis of the ankle joint among the pediatric population. We present a case of a 9-year-old boy with synovial chondromatosis of the left ankle.

CASE REPORT

A 9-year-old boy had synovial osteochondromatosis in the left ankle joint, which caused pain, swelling, and restriction of movement of the left ankle. Radiological examinations showed variable size calcific foci adjacent to the medial malleolus and medial ankle joint space with mild soft-tissue swelling. The ankle mortise space was well-maintained. The magnetic resonance imaging of the ankle joint revealed a benign synovial neoplastic process and a few focal marrows containing loose bodies. The synovium was thick, and there was no articular erosion. The patient was planned and underwent an en bloc resection. A lobulated pearly white mass arising from the ankle joint was observed intraoperatively. Histological examination also showed attenuated synovium with osteocartilaginous nodule with binucleated and multinucleated forms of chondrocyte typical of osteochondroma were appreciated. Endochondral ossification, mature bony trabeculae with intervening fibro adipose tissue, was noted. The patient had remarkable relief of clinical complaints and was almost asymptomatic at the time of the first follow-up.

CONCLUSION

Synovial chondromatosis may present with diverse clinical manifestations according to the different stages of the disease as described by Milgram; like joint pain, limitation of movements, swelling due to the close proximity of important structures including joints, tendons, and neurovascular bundles. A simple radiograph with a characteristic appearance is usually sufficient in confirming the diagnosis. In pediatric patients, overlooking these conditions may result in growth abnormality, skeletal deformities, and several mechanical problems. We suggest that when dealing with the case of swelling in or around the ankle, the differential diagnosis should include synovial chondromatosis.

摘要

引言

滑膜软骨瘤病并不常见,踝关节受累极为罕见。在儿科人群中,我们仅发现一例踝关节滑膜软骨瘤病。我们报告一例9岁男孩左侧踝关节滑膜软骨瘤病的病例。

病例报告

一名9岁男孩左侧踝关节患有滑膜骨软骨瘤病,导致左侧踝关节疼痛、肿胀及活动受限。影像学检查显示内踝及内侧踝关节间隙附近有大小不一的钙化灶,伴有轻度软组织肿胀。踝关节榫眼间隙保持良好。踝关节磁共振成像显示为良性滑膜肿瘤性病变,并有一些含有游离体的局灶性骨髓。滑膜增厚,无关节侵蚀。该患者计划并接受了整块切除。术中观察到一个从踝关节长出的分叶状珍珠白色肿物。组织学检查还显示滑膜变薄,有骨软骨结节,可见典型骨软骨瘤的双核和多核软骨细胞形式。观察到软骨内成骨,有成熟的骨小梁及其间的纤维脂肪组织。该患者临床症状明显缓解,首次随访时几乎无症状。

结论

如米尔格拉姆所描述,滑膜软骨瘤病可能根据疾病的不同阶段呈现出多样的临床表现;如关节疼痛、活动受限、因靠近包括关节、肌腱和神经血管束等重要结构而肿胀。具有特征性表现的简单X线片通常足以确诊。在儿科患者中,忽视这些情况可能导致生长异常、骨骼畸形和一些机械问题。我们建议,在处理踝关节内或周围肿胀的病例时,鉴别诊断应包括滑膜软骨瘤病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8171/10182579/c11b01b09320/JOCR-13-5-g001.jpg

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