Peripheral soft tissue Ewing’s sarcoma: a rare case report

F. Shegufta, M. Ferdousi, A. Taher
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Abstract

A 22 years male patient presented with gradual left forearm swelling for 6 months. X ray forearm revealed large soft tissue swelling with tiny calcification and mild scalloping at inner aspect of ulna and ultrasonogram (USG) revealed soft tissue mass having calcification and necrotic areas within and spectral Doppler showed arterial type of blood flow with no augmentation. Later computerized tomography (CT) scan showed soft tissue mass with necrotic area and calcification with no bony involvement. Magnetic resonance imaging (MRI) with contrast revealed a large heterogeneously enhancing lobulated mixed intensity lesion in antero-medial compartment of the left forearm involving flexor group of muscles causing displacement of fat plane. MRI and subsequent histopathology of the lesion revealed it as a rare soft tissue Ewing’s sarcoma / primitive neuroectodermal tumor (PNET) in extremity. DOI: http://dx.doi.org/10.3329/imcj.v7i2.20113 Ibrahim Med. Coll. J. 2013; 7(2): 43-46
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外周软组织尤文氏肉瘤1例
22岁男性患者表现为左前臂逐渐肿胀6个月。前臂X线示大面积软组织肿胀伴微小钙化,尺骨内侧轻度成扇形,超声示软组织肿块伴钙化坏死,超声多普勒示动脉型血流,无增强。后来的计算机断层扫描(CT)显示软组织肿块坏死区和钙化,没有骨受累。磁共振成像(MRI)显示左前臂前内侧隔室一大块不均匀增强的分叶状混合强度病变,累及屈肌群,导致脂肪平面移位。MRI及病理检查显示为一罕见的四肢软组织尤文氏肉瘤/原始神经外胚层肿瘤。DOI: http://dx.doi.org/10.3329/imcj.v7i2.20113 Ibrahim Med. col。j . 2013;7 (2): 43-46
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