关键词: Health supervision Imaging examination Neurofibromatosis type 1 Plexiform neurofibroma Surgical treatment

Mesh : Child, Preschool Female Humans Infant Neurofibroma / complications diagnosis surgery Neurofibroma, Plexiform / diagnosis pathology surgery Neurofibromatosis 1 / complications diagnosis pathology Orbital Neoplasms

来  源:   DOI:10.1016/j.ctarc.2022.100582

Abstract:
This article has been retracted: please see Elsevier Policy on Article Withdrawal (http://www.elsevier.com/locate/withdrawalpolicy). This article has been retracted at the request of the Authors. A diagnostic discordance in the original pathology reports has been noticed and requires further evaluation, therefore the paper will be retracted.
摘要:
1型神经纤维瘤病是一种罕见的遗传性疾病,这是一种良性神经肿瘤,由神经鞘细胞的异常生长引起。NF1患者与多系统受累有关,以神经纤维瘤为特征,其中50%与神经丛神经纤维瘤有关。特征性良性丛状神经纤维瘤可引起疼痛,毁容,压缩和功能变化。尽管丛状神经纤维瘤常见于头颈部,眼眶丛状神经纤维瘤罕见,容易与其他眼眶肿瘤混淆。关于丛状神经纤维瘤的治疗策略尚无共识,目前的治疗主要是手术,但部分切除后复发率高。我们描述了一例4岁的眼眶丛状神经纤维瘤患者,其右眼有3年的下垂史。一开始,我们误诊为血管瘤.手术切除后,经组织病理学检查证实为丛状神经纤维瘤。手术一年后,肿瘤复发了,所以再次进行了手术切除,眼睑下垂得到纠正。之后,每年对患者进行随访和检查,到目前为止没有发现复发。此病例表明,应评估单侧眼睛肿胀和上眼睑下垂的婴儿或儿童的眼眶神经纤维瘤。
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