Ewing's Sarcoma of the Scapula in an Infant: About a Case

A. Dinga, F. Niyongere, N. Allaoui, A. Dendane, A. Amrani, Alami Alami, T. Madhi
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Abstract

Ewing sarcoma (ES)/primary neuroectodermal tumor (PNET) is the second most common malignant bone tumor of childhood and adolescence. It can occur at central or peripheral sites, at skeletal or extraskeletal sites, and is more common at the femurs, ilium, and tibia. We report a rare case of Ewing's sarcoma of the scapula in a 2-year-old infant diagnosed with pain and swelling of the left shoulder. Histopathological confirmation of Ewing's sarcoma was possible following ultrasound-guided biopsy. Treatment consisted of initial chemotherapy, followed by surgical tumor resection after good initial response, followed by adjuvant therapy. The current post-treatment follow-up is 2 years without incident. This case is reported to highlight the rarity of localization and therapeutic modalities, particularly surgical.
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婴儿肩胛骨尤文氏肉瘤:关于一个病例
尤文肉瘤(ES)/原发性神经外胚层瘤(PNET)是儿童和青少年时期第二常见的恶性骨肿瘤。它可发生在中央或周围部位,骨骼内或骨骼外部位,股骨、髂骨和胫骨更为常见。我们报告了一例罕见的肩胛骨尤文氏肉瘤病例,患者为一名两岁婴儿,因左肩部疼痛和肿胀而确诊。经超声引导活检后,组织病理学确诊为尤文氏肉瘤。治疗包括初始化疗,在初期反应良好后进行肿瘤手术切除,然后进行辅助治疗。目前,治疗后随访 2 年,未发生任何意外。本病例的报告旨在强调定位和治疗方式的罕见性,尤其是手术治疗。
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