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Extensive plexiform neurofibroma in a premature neonate

机译:早产儿广泛性丛状神经纤维瘤

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We describe a premature neonate with an extensive plexiform neurofibroma. Prenatal ultrasound at 32 weeks of gestation was normal. Postnatal examination was significant for a palpable left neck mass. Magnetic resonance imaging (MRI) of the head demonstrated a mass involving the left cavernous sinus with spreading to the left orbital region. MRI of the neck was positive for extensive adenopathy, left more than right, with extension into the deep face region and infratemporal fossa on the left side. MRI of the chest, abdomen, and pelvis demonstrated a mass extending from the superior mediastinum to the left pelvic retroperitoneal region, including the mesenteric vasculature and spinal canal at multiple levels with compression of the spinal cord. Biopsy of the left neck mass confirmed for plexiform neurofibroma. A careful search of the literature revealed no previous report of such an extensive neurofibroma in a premature neonate. Surgical decompression in this premature neonate was not possible because of the extensive nature of the disease; it is known that neurofibroma is non-respondent to chemotherapy and radiotherapy. Therefore, alternative treatment is needed to improve the outcome.
机译:我们描述了一个广泛的丛状神经纤维瘤的早产儿。妊娠32周时的产前超声检查正常。产后检查对于可触知的左颈部肿块很重要。头部的磁共振成像(MRI)显示肿块累及左海绵窦,并扩散到左眼眶区域。颈部MRI表现为广泛的腺病阳性,左侧多于右侧,延伸至深面部区域和左侧颞下窝。胸部,腹部和骨盆的MRI显示肿块从上纵隔延伸到左侧盆腔腹膜后区域,包括肠系膜脉管系统和脊髓受压的多个水平的椎管。左颈部肿物的活检证实为丛状神经纤维瘤。仔细研究文献发现,以前没有关于早产新生儿如此广泛的神经纤维瘤的报道。由于该疾病的广泛性,无法在该早产儿进行手术减压。已知神经纤维瘤对化学疗法和放射疗法无反应。因此,需要替代治疗以改善结果。

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