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成年男性股骨头部罕见内生软骨瘤病例报告

A Rare Occurrence of Enchondroma in the Head of Femur in an Adult Male: A Case Report.

作者信息

Satti Lakshmana Reddy, Yennapu Nageswara Rao, Inturi Rohit, Surada Ramakrishna

机构信息

Department of Orthopaedic Surgery, GGH, Rangaraya Medical College, Kakinada, Andhra Pradesh, India.

出版信息

J Orthop Case Rep. 2023 Apr;13(4):62-65. doi: 10.13107/jocr.2023.v13.i04.3618.

Abstract

INTRODUCTION

Enchondroma is a solitary, benign, and intramedullary cartilaginous tumor occurring most commonly in small bones of hands and feet contributing to 3-10% of all bone tumors. They originate from the growth plate cartilage which later on proliferates to form enchondroma. Lesions are central or eccentric and metaphyseal involvement is most common for long bones. We report a case of atypical occurrence of enchondroma in the head of femur in a young male.

CASE REPORT

A 20-year-old male patient presented with a history of pain in the left groin for 5 months. Radiological examination showed a lytic lesion in the head of femur. The patient was managed by safe surgical dislocation of the hip, curettage with autogenous iliac crest bone graft with countersunk screw fixation. Histopathology confirmed the lesion to be enchondroma. At the latest follow-up after 6 months, the patient was symptom-free and there was no evidence of any recurrence.

CONCLUSION

Lytic lesions in the neck femur can have a good prognosis provided timely diagnosis and interventions are done. The present case of enchondroma in the head of femur represents a very rare differential diagnosis for the same and this must be kept in mind. So far, no such case has been reported in the literature. Magnetic resonance imaging and histopathology are of the essence to confirm this entity.

摘要

引言

内生软骨瘤是一种孤立性、良性的髓内软骨肿瘤,最常见于手和足部的小骨,占所有骨肿瘤的3% - 10%。它们起源于生长板软骨,随后增殖形成内生软骨瘤。病变可为中心性或偏心性,长骨最常累及干骺端。我们报告一例年轻男性股骨头部非典型内生软骨瘤病例。

病例报告

一名20岁男性患者,有左侧腹股沟疼痛5个月的病史。影像学检查显示股骨头部有溶骨性病变。患者接受了髋关节安全手术脱位、自体髂骨植骨刮除术及埋头螺钉固定治疗。组织病理学证实病变为内生软骨瘤。在6个月后的最新随访中,患者无症状,无任何复发迹象。

结论

股骨颈溶骨性病变如果能及时诊断并进行干预,预后良好。本例股骨头部内生软骨瘤是该部位非常罕见的鉴别诊断情况,必须予以考虑。迄今为止,文献中尚未报道过此类病例。磁共振成像和组织病理学对于确诊该疾病至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3443/10182580/bf67ee26f16d/JOCR-13-62-g001.jpg

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