Al Khader Ali, Nsour Esra, Al-Zubi Raneem Bassam, Al Maadat Hakam Mansor Dahar
Faculty of Medicine, Al-Balqa Applied University, Full-time lecturer of pathology.
Department of pathology, Al Hussein Salt Hospital, Ministry of Health, Al-Salt.
Medicine (Baltimore). 2019 Apr;98(15):e15207. doi: 10.1097/MD.0000000000015207.
Extraskeletal myxoid chondrosarcoma is a slow-growing soft tissue tumor of adults with a propensity for local recurrence and eventual metastasis. Only 17 pediatric and adolescent cases have been reported.
Here we present an 11-year-old boy with a 3-year history of a slowly growing painless left leg mass. Magnetic resonance imaging of the lesion revealed a subfascial well-circumscribed lesion with intramuscular extension in the medial gastrocnemius muscle of the left leg.
He underwent wide local excision of the mass and the histomorphological and immunohistochemical findings were consistent with extraskeletal myxoid chondrosarcoma.
Possible radiotherapy was the further management plan.
He was in good condition with no evidence of recurrence at 6 months postsurgery.
Although pediatric cases of extraskeletal myxoid chondrosarcoma were reported to be aggressive, the tumor in this case demonstrated indolent behavior. Furthermore, the tumor in this case showed primitive round cell foci which adds to a previous study that especially reported this morphology in pediatric cases.
骨外黏液样软骨肉瘤是一种成人的生长缓慢的软组织肿瘤,有局部复发和最终转移的倾向。仅报道过17例儿童和青少年病例。
我们在此报告一名11岁男孩,左腿有一个缓慢生长的无痛性肿块,病史3年。对该病变进行的磁共振成像显示,在左腿腓肠肌内侧有一个筋膜下边界清楚的病变,并向肌内延伸。
他接受了肿块的广泛局部切除,组织形态学和免疫组化结果符合骨外黏液样软骨肉瘤。
进一步的治疗计划是可能进行放疗。
术后6个月时他情况良好,无复发迹象。
虽然据报道骨外黏液样软骨肉瘤的儿童病例具有侵袭性,但该病例中的肿瘤表现为惰性。此外,该病例中的肿瘤显示有原始圆形细胞灶,这补充了之前一项特别报道儿童病例中这种形态的研究。