Köse Doğan, Annagür Ali, Erol Cengiz, Uğraş Serdar, Köksal Yavuz
Department of Pediatric Oncology, Selcuk University Faculty of Medicine, Konya, Turkey.
Pediatr Int. 2014 Jun;56(3):e17-20. doi: 10.1111/ped.12338.
Synovial sarcoma is rarely detected in infants, with an annual incidence of 0.5 per million. Synovial sarcoma occurs more frequently in adolescents and young adults, with the majority of patients presenting between 15 and 40 years of age. It is extremely rare, however, in pediatric patients under 2 years of age. In the present study we examined a 3-day-old male infant born at 32 weeks who had a mass on his left arm. Synovial sarcoma was identified on histopathological and immunohistochemical analysis of biopsy material acquired from the mass. On whole body magnetic resonance imaging, diffuse metastases were detected in the bilateral lungs in the retroperitoneal zone, in bilateral suprarenal glands, the right liver lobe, the right kidney, and the brain. To our knowledge this is the youngest patient to be diagnosed with synovial sarcoma in the literature.
滑膜肉瘤在婴儿中很少见,年发病率为百万分之0.5。滑膜肉瘤在青少年和年轻人中更常见,大多数患者发病年龄在15至40岁之间。然而,在2岁以下的儿科患者中极为罕见。在本研究中,我们检查了一名32周出生的3天大男婴,其左臂有一个肿块。对从肿块获取的活检材料进行组织病理学和免疫组织化学分析后,确诊为滑膜肉瘤。在全身磁共振成像检查中,发现双侧肺部、腹膜后区域、双侧肾上腺、右肝叶、右肾和脑部有弥漫性转移。据我们所知,这是文献中诊断为滑膜肉瘤的最年轻患者。