Brown Desmond A, Deep Nicholas L, Driscoll Colin L, Link Michael J, Jentoft Mark E, Daniels David J
Departments of1Neurological Surgery.
2Otorhinolaryngology, and.
J Neurosurg Pediatr. 2018 Sep;22(3):283-287. doi: 10.3171/2018.3.PEDS17609. Epub 2018 Jun 15.
Epstein-Barr virus-associated smooth-muscle tumors are rare tumors seen in immunocompromised patients. Most cases occur in the context of AIDS and organ transplantation, and very rarely in the setting of congenital immunodeficiency, with only 5 case reports of the latter published so far in the literature. The authors report the case of a previously healthy 8-year-old girl with headaches and precocious puberty who was found to have a large skull base lesion. There was a synchronous left adrenal lesion. She underwent resection of the skull base lesion and a left adrenalectomy. Thorough evaluation for immunodeficiency was negative for a known congenital immunodeficiency syndrome. She had a short course of intravenous immunoglobulin and has had no recurrence of disease or new lesions in the 17 months since presentation. Continued surveillance for the development of opportunistic infections and new or recurrent lesions is warranted in this case. Repeat surgery for surgically accessible tumors or chemoradiation would be recommended for any additional lesions.
爱泼斯坦-巴尔病毒相关的平滑肌瘤是免疫功能低下患者中罕见的肿瘤。大多数病例发生在艾滋病和器官移植的背景下,在先天性免疫缺陷的情况下非常罕见,迄今为止文献中仅发表了5例后者的病例报告。作者报告了一例先前健康的8岁女孩,有头痛和性早熟症状,发现有一个巨大的颅底病变。同时还有一个左侧肾上腺病变。她接受了颅底病变切除术和左侧肾上腺切除术。对免疫缺陷进行的全面评估排除了已知的先天性免疫缺陷综合征。她接受了短期静脉注射免疫球蛋白治疗,自就诊以来的17个月里没有疾病复发或新病变。对于该病例,有必要持续监测机会性感染的发生以及新的或复发性病变。对于任何其他可手术切除的肿瘤,建议重复手术或进行放化疗。