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胫骨骨干内生软骨瘤——病例报告及其在骨干中的特征与鉴别诊断综述

Enchondroma in the Diaphysis of Tibia - A Case Report and Review of its Characteristics and Differentials in the Diaphysis.

作者信息

Nayak Keerthan Ranga, Kulkarni Mahesh Suresh, Vijayan Sandeep, Rao Sharath Kumar

机构信息

Department of Orthopaedics, Kasturba Medical College Manipal, Manipal Academy of Higher Education, Manipal, Karnataka, India.

出版信息

J Orthop Case Rep. 2021 Jul;11(7):6-11. doi: 10.13107/jocr.2021.v11.i07.2292.

Abstract

INTRODUCTION

Enchondroma is a solitary, benign, intramedullary cartilaginous tumor commonly noticed in the phalanges of hands and feet with characteristic radiological features. Its occurrence in aberrant sites with atypical features lead to diagnostic dilemma. Enchondromas which are usually managed non-operatively can mimic other benign and malignant lesions, especially chondrosarcoma.

CASE REPORT

We report the case of a 31-year-old farmer who presented with long standing inconspicuous pain in his left leg which turned out to be a diaphyseal enchondroma even though it demonstrated aggressive radiological features mimicking a chondrosarcoma. Incisional biopsy was done from the scalloped areas to obtain the correct histological diagnosis. He underwent thorough curettage of the lesion and remains asymptomatic 2 years after the procedure. We attempt to discuss the differentials which the orthopedic surgeon should keep in mind for diaphyseal lesions mimicking enchondroma.

CONCLUSION

Though classically found in metaphysis, Enchondromas are not uncommon in diaphysis of long bones. Enchondromas are generally benign, but can cause diagnostic dilemma when they present with aggressive features at rare locations and surgeons should be wary of the differentials. Despite a size of more than 6 cm and evidence of cortical erosion and intramedullary widening, the lesion could still be benign. Early biopsy will help to differentiate Enchondroma from a malignant transformation or malignant tumor.

摘要

引言

内生软骨瘤是一种孤立性、良性的髓内软骨肿瘤,常见于手足的指(趾)骨,具有特征性的放射学表现。其在具有非典型特征的异常部位发生会导致诊断困境。通常采用非手术治疗的内生软骨瘤可能会模仿其他良性和恶性病变,尤其是软骨肉瘤。

病例报告

我们报告一例31岁农民的病例,他左腿长期存在不明显的疼痛,结果发现是骨干内生软骨瘤,尽管其放射学表现具有侵袭性,类似软骨肉瘤。从扇贝样区域进行了切开活检以获得正确的组织学诊断。他接受了病变的彻底刮除术,术后2年仍无症状。我们试图讨论骨科医生对于模仿内生软骨瘤的骨干病变应牢记的鉴别诊断。

结论

尽管内生软骨瘤经典地见于干骺端,但在长骨骨干中也并不罕见。内生软骨瘤一般为良性,但当它们在罕见部位表现出侵袭性特征时会导致诊断困境,外科医生应警惕鉴别诊断。尽管病变大小超过6cm且有皮质侵蚀和髓内增宽的证据,但该病变仍可能是良性的。早期活检有助于将内生软骨瘤与恶性转化或恶性肿瘤区分开来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e849/8576783/8a0c6d3b8b2f/JOCR-11-6-g001.jpg

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