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©The Author(s) 2022.
World J Clin Cases. Jul 6, 2022; 10(19): 6595-6601
Published online Jul 6, 2022. doi: 10.12998/wjcc.v10.i19.6595
Published online Jul 6, 2022. doi: 10.12998/wjcc.v10.i19.6595
Figure 1 Sonography of the soft tissue mass in the neck.
A and B: At the grey scale images, a soft tissue mass consisted of hypoechoic and anechoic was found in the right neck with the measurement of 33 mm × 27 mm × 28 mm on the longitudinal section and transection; C: Internal vascularity was present on Doppler images.
Figure 2 The soft tissue mass was indicated on the transverse plane, coronal plane and sagittal plane from 3.
0 T magnetic resonance imaging scan. A: A well-defined lesion located in the right laryngeal and piriform recess present as heterogeneous equisignal intensity on T1 -weighted image; B, D and F: High signal intensity on T2 -weighted images; C, E and G: Moreover, the contrast enhanced MRI scan displayed the prominent and heterogeneous contrast enhancement with fast perfusion mode in the early arterial phase on T1+C images.
Figure 3 Pathological gross images of the lesion.
A: The dark red mass was completely enveloped in well-defined capsule; B: It was elucidated to be multilocular cystic when split.
Figure 4 Histologic specimen (immunohistochemical stain, immunohistochemistry; original magnification, × 400) confirmed a diagnosis of the extraskeletal Ewing sarcoma, with the small round blue-stained cells observed.
Immunochemical histological findings: NSE(+), NF(-), INI-1(+++), TTF-1(-), CK20(-), TDT(-), Wilms tumor(-), Bcl-2(+++), Ki-67(+), CD34(-), CD99(+++), Vimentin(+++), Syn(+).
- Citation: Chen ZH, Guo HQ, Chen JJ, Zhang Y, Zhao L. Imaging-based diagnosis for extraskeletal Ewing sarcoma in pediatrics: A case report . World J Clin Cases 2022; 10(19): 6595-6601
- URL: https://www.wjgnet.com/2307-8960/full/v10/i19/6595.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v10.i19.6595