Yalçın Koray, Tüysüz Gülen, Kazan Saim, Gürer Elif İnanç, Karaali Kamil, Küpesiz Alphan, Güler Elif
Departments Pediatric Hematology and Oncology, Akdeniz University Faculty of Medicine, Antalya, Turkey.
Department Neurosurgery, Akdeniz University Faculty of Medicine, Antalya, Turkey.
Turk J Pediatr. 2019;61(5):765-770. doi: 10.24953/turkjped.2019.05.017.
Yalçın K, Tüysüz G, Kazan S, Gürer Eİ, Karaali K, Küpesiz A, Güler E. An infant with intradural extramedullary synovial sarcoma: the youngest case in the literature. Turk J Pediatr 2019; 61: 765-770. Spinal cord involvement of synovial sarcoma is extremely rare. So far only two cases have been reported. Herein we describe the youngest case in the literature. She is 14-month-old and first presented with difficulty in walking ongoing for a week. Imagining showed a spinal cord mass at C5-T3 levels. The patient had gone under Decompressive surgery and histopathologic examination of the specimen revealed the presence of synovial sarcoma. Although the tumor regressed after chemotherapy, she was lost due to viral pneumonia. Synovial sarcoma should be kept in mind while evaluating spinal tumors even in infantile group.
亚尔钦·K、图伊苏兹·G、卡赞·S、居雷尔·Eİ、卡拉利·K、屈佩西兹·A、居勒尔·E。一名患有硬脊膜内髓外滑膜肉瘤的婴儿:文献中最年幼的病例。《土耳其儿科学杂志》2019年;61: 765 - 770。滑膜肉瘤累及脊髓极为罕见。迄今为止仅报道过两例。在此我们描述文献中最年幼的病例。她14个月大,首次因持续一周的行走困难就诊。影像学检查显示C5 - T3水平有脊髓肿物。患者接受了减压手术,标本的组织病理学检查显示存在滑膜肉瘤。尽管化疗后肿瘤缩小,但她因病毒性肺炎去世。即使在婴儿组评估脊髓肿瘤时也应考虑到滑膜肉瘤。