AlQatie Ahmad, Abbod Hatem, Alzaid Tariq, Alsolami Afaf
Department of Radiology, King Faisal Specialist Hospital and Research Center, Riyadh, SAU.
Department of Radiology, Salmaniya Medical Complex, Manama, BHR.
Cureus. 2024 Jan 28;16(1):e53132. doi: 10.7759/cureus.53132. eCollection 2024 Jan.
Background Congenital/infantile fibrosarcoma is a rare soft tissue tumor presented in early age of life. It should be considered in the differential diagnosis of the large soft tissue masses especially in the extremities at the age of infancy. These tumors frequently are misdiagnosed at birth as hemangioma. Histologically, they can resemble their adult counterparts and they are characterized by the chromosomal translocation t(12;15) (p13;q25) resulting in the gene fusion. Objective A retrospective review of the MRI features of histopathology-proven congenital/infantile fibrosarcoma provides our own institutional experience and supports the limited radiology literature written about this disease. Material and method The list of our patients is obtained after reviewing our radiology and pathology database in the period between June 1st, 2007 and May 31st, 2017 (10 years) at King Faisal Specialist Hospital & Research Center, Riyadh. Phrases used to search in our MRI examinations database are: congenital infantile fibrosarcoma, infantile fibrosarcoma, juvenile fibrosarcoma, soft tissue sarcoma, malignant soft tissue mass, sarcomatous soft tissue mass, fibrosarcoma, spindle cell sarcoma, myomatous sarcoma. Result In our database and picture archiving and communication system (PACS) during the period of the study, the word (fibrosarcoma) was mentioned in the radiology report of 182 patients. Only four cases were histopathologically proven to be a congenital/infantile fibrosarcoma and had completed their own MR exams - three of them were primary/new cases, males with an age range between 0 days and 5 months (median age: 5 months). The fourth case was a female with a history of 1 presentation at the age of one month and proved by histopathology examination but there was no available imaging at that time; however, tumor recurrence in the same patient was at the age of 4 years with available MR imaging and pathology sample. Conclusion Congenital infantile fibrosarcoma is a rare entity that has no specific MRI findings. However, it should be always considered as part of the differential diagnosis of congenital soft tissue masses with aggressive behavior.
背景 先天性/婴儿纤维肉瘤是一种罕见的软组织肿瘤,出现在生命早期。在鉴别诊断尤其是婴儿期四肢的大软组织肿块时应考虑到该病。这些肿瘤在出生时经常被误诊为血管瘤。在组织学上,它们可能类似于成人的同类肿瘤,其特征是染色体易位t(12;15)(p13;q25)导致基因融合。目的 对经组织病理学证实的先天性/婴儿纤维肉瘤的MRI特征进行回顾性研究,提供我们自己机构的经验,并支持关于这种疾病的有限放射学文献。材料和方法 在利雅得法赫德国王专科医院及研究中心回顾2007年6月1日至2017年5月31日(10年)期间的放射学和病理学数据库后,获取我们的患者名单。用于在我们的MRI检查数据库中搜索的短语有:先天性婴儿纤维肉瘤、婴儿纤维肉瘤、青少年纤维肉瘤、软组织肉瘤、恶性软组织肿块、肉瘤样软组织肿块、纤维肉瘤、梭形细胞肉瘤、肌瘤样肉瘤。结果 在研究期间我们的数据库和图像存档与通信系统(PACS)中,182例患者的放射学报告中提到了“纤维肉瘤”一词。只有4例经组织病理学证实为先天性/婴儿纤维肉瘤且完成了自身的MR检查——其中3例为原发性/新病例,男性,年龄在0天至5个月之间(中位年龄:5个月)。第4例是一名女性,1个月时曾有1次就诊史,经组织病理学检查证实,但当时没有可用的影像学资料;然而,该患者在4岁时肿瘤复发,有可用的MR成像和病理样本。结论 先天性婴儿纤维肉瘤是一种罕见的疾病,没有特异性的MRI表现。然而,它应始终被视为具有侵袭性表现的先天性软组织肿块鉴别诊断的一部分。