Gupta Aditya Kumar, Jones Michael, Prelog Kristina, Bui John, Zhu Jacqui, Ng Anthea, Dalla-Pozza Luciano
a Department of Oncology , Children's Hospital at Westmead , Sydney , New South Wales , Australia.
b Department of Ophthalmology , Children's Hospital at Westmead , Sydney , New South Wales , Australia.
Pediatr Hematol Oncol. 2016 Sep;33(6):408-414. doi: 10.1080/08880018.2016.1225326. Epub 2016 Sep 30.
Patients with familial/heritable retinoblastoma (RB) are at increased risk of developing second malignancies throughout life, including a pineoblastoma (trilateral RB [TRB]) in early childhood. Current guidelines recommend regular surveillance brain imaging for those with heritable RB until 5 years of age. The presence of pineal cysts has been reported in patients with RB. Pineal cysts are thought to arise due to focal degeneration of the pineal gland and can be found incidentally. The finding of pineal abnormalities including cysts in children with RB on imaging is disconcerting, as it raises the possibility of an underlying malignancy, specifically a pinealoblastoma. The authors reviewed the imaging findings and clinical significance of pineal cysts in 69 patients diagnosed with RB at our center between December 1999 and November 2015. Twenty-six patients had pineal cysts found on brain magnetic resonance imaging (MRI) scans performed either at diagnosis or follow-up. Thirty-eight of 69 patients had underlying heritable RB. Nineteen of 38 familial RB patients had a pineal cyst compared with 3 out of 26 with sporadic RB (P = .004). In the majority, the imaging characteristics and size of the cysts remained stable or resolved. In this cohort, pineal cysts were detected at significantly increased frequency in heritable RB. This may be a benign association or may reflect abnormal underlying biology of pineal tissue in individuals highly susceptible to malignancy. Imaging characteristics can be helpful in distinguishing between benign and malignant lesions. The presence of a pineal cyst in patients with unilateral disease may be a useful indicator of underlying heritable RB.
患有家族性/遗传性视网膜母细胞瘤(RB)的患者一生中发生第二原发性恶性肿瘤的风险增加,包括儿童早期发生松果体母细胞瘤(三边性RB [TRB])。当前指南建议对遗传性RB患者进行定期的脑部影像学监测,直至5岁。已有报道RB患者存在松果体囊肿。松果体囊肿被认为是由于松果体局灶性变性引起的,可偶然发现。在RB患儿的影像学检查中发现包括囊肿在内的松果体异常令人不安,因为这增加了潜在恶性肿瘤,特别是松果体母细胞瘤的可能性。作者回顾了1999年12月至2015年11月期间在我们中心诊断为RB的69例患者的松果体囊肿的影像学表现及临床意义。26例患者在诊断或随访时进行的脑部磁共振成像(MRI)扫描中发现了松果体囊肿。69例患者中有38例患有遗传性RB。38例家族性RB患者中有19例存在松果体囊肿,而26例散发性RB患者中有3例存在松果体囊肿(P = 0.004)。大多数情况下,囊肿的影像学特征和大小保持稳定或消退。在该队列中,遗传性RB患者中松果体囊肿的检出频率显著增加。这可能是一种良性关联,也可能反映了对恶性肿瘤高度易感个体的松果体组织潜在生物学异常。影像学特征有助于区分良性和恶性病变。单侧病变患者中存在松果体囊肿可能是遗传性RB的一个有用指标。