Malignant transformation in an 11-year-old child with multiple hereditary exostosis

Janet L de Stadler, N. Kruger, Shivani Singh, E. Banderker, S. Dix-Peek, K. Pillay
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Abstract

ABSTRACT BACKGROUND: Multiple hereditary exostosis (MHE) is a rare autosomal dominant disorder predisposing to the development of multiple osteochondromas. Malignant transformation is an uncommon complication of osteochondromas and is especially rare in the paediatric population. Making a diagnosis of malignant transformation is recognised as a challenge globally METHODS: We obtained informed consent and ethics approval prior to reviewing the hospital file, radiology and pathology of our index patient, as well as conducting a directed literature search RESULTS: An 11-year-old male with MHE presented with new onset pain in the right leg with an associated inability to weight bear. Plain radiographs and magnetic resonance imaging (MRI) showed features consistent with malignant transformation. The child underwent a Malawer 1 resection of the proximal fibula with no complications. The pathology confirmed a grade 1 secondary peripheral chondrosarcoma (CS) arising in an osteochondroma The rate of malignant transformation in MHE is as high as 36.3% in select specialist tertiary centres. Ninety per cent of the resultant malignancies are chondrosarcomas. Malignant transformation before the age of 20 years is exceptional. Plain radiology is routinely used for monitoring of patients with MHE. Other modalities exist to assess for cartilage cap thickness, a much-debated criterion of malignant change. Pathology is essential for confirmation of malignant transformation as well as to exclude high grade lesions. Treatment is wide local excision (WLE) with limb-sparing surgery and long-term follow-up to detect for local recurrences. CONCLUSION: The malignant transformation of osteochondromas occurs more frequently in individuals with MHE and may even arise in the paediatric population. In the presence of suspicious clinical or radiological features, en-bloc surgical resection and histopathological correlation is mandatory to make the diagnosis. We encourage a multidisciplinary team approach with collaboration between the orthopaedic surgeon, radiologist and pathologist Level of evidence: Level 5 Keywords: multiple hereditary exostosis (MHE), chondrosarcoma, osteochondroma, malignant transformation
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一例11岁儿童多发性遗传性外泌体病的恶性转化
背景:多发性遗传性外生骨病(MHE)是一种罕见的常染色体显性遗传病,易导致多发性骨软骨瘤的发生。恶性转化是骨软骨瘤的罕见并发症,在儿科人群中尤其罕见。方法:在审查医院档案、放射学和病理之前,我们获得了知情同意和伦理批准,并进行了有针对性的文献检索。结果:一名11岁男性MHE患者,右腿新发疼痛,并伴有无法负重。x线平片和磁共振成像(MRI)显示与恶性转化相符的特征。该患儿接受了腓骨近端Malawer 1切除术,无并发症。病理证实由骨软骨瘤引起的1级继发性外周软骨肉瘤(CS)。在一些专科三级中心,MHE的恶性转化率高达36.3%。90%的恶性肿瘤是软骨肉瘤。20岁以前的恶性转化是罕见的。常规影像学检查用于MHE患者的监测。评估软骨帽厚度的其他方式存在,这是一个备受争议的恶性变化标准。病理是必要的恶性转化的确认,并排除高级别病变。治疗是广泛的局部切除(WLE)与肢体保留手术和长期随访,以发现局部复发。结论:骨软骨瘤的恶性转化在MHE患者中更常见,甚至可能出现在儿科人群中。在存在可疑的临床或放射学特征时,必须进行整体手术切除和组织病理学相关才能做出诊断。我们鼓励骨科医生、放射科医生和病理学家开展多学科合作。证据等级:5级。关键词:多发性遗传性外生性增生(MHE)、软骨肉瘤、骨软骨瘤、恶性转化
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来源期刊
SA Orthopaedic Journal
SA Orthopaedic Journal Medicine-Orthopedics and Sports Medicine
CiteScore
0.40
自引率
0.00%
发文量
17
审稿时长
6 weeks
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