Imaging-based diagnosis for extraskeletal Ewing sarcoma in pediatrics: A case report

被引:0
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作者
Zhi-Hui Chen [1 ]
He-Qing Guo [2 ]
Jing-Jing Chen [3 ]
Ying Zhang [4 ]
Li Zhao [5 ]
机构
[1] Medical Ultrasound, Affiliated Lishui Hospital of Zhejiang University, The Fifth Affiliated Hospital of Wenzhou Medical University, The Central Hospital of Zhejiang Lishui
[2] Medical Ultrasound, Women and Children Hospital of Shaoxing
[3] Electrocardiogram Room, Cixi integrated Traditional Chinese and Western Medicine Medical, Health Group Cixi Hospital of Traditional Chinese Medicine
[4] Medical Ultrasound, Ningbo Medical Center Lihuili Hospital
[5] Department of Radiology, Shaoxing People's Hospital
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中图分类号
R738.1 [骨骼肿瘤];
学科分类号
100214 ;
摘要
BACKGROUND Extraskeletal Ewing sarcoma(EES) is a member of the Ewing sarcoma family of tumors which is pathologically known as a small, round, blue cell tumor involving bone and soft tissue. The prevalence of EES is only 15%-25% of all Ewing sarcoma and EES often occurs in patients aged from 20-mo-old to 30-yearsold resulting in an unfavorable prognosis.CASE SUMMARY The present case report described a 7-year-old patient with a palpable EES mass of 33 mm × 27 mm × 28 mm in the deep neck with symptoms of persistent dyspnea over the past 5 mo. After laboratory examinations, abnormal physiological and biochemical indicators were not found. Ultrasound images presented the mass to be complex, solid and fluid-filled with circumscribed margins and posterior acoustic enhancement. The mass also presented with partial internal vascularity. The contrast-enhanced magnetic resonance imaging scan illustrated the outstanding enhancement with fast perfusion mode in the early arterial phase.CONCLUSION Our study suggested that a quick-growing mass in the pediatric patient is possibly a malignant tumor whether the mass has well-defined margins or not.
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页码:6595 / 6601
页数:7
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