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An Exceptional Case of Intraparotid Plexiform Neurofibroma Originating from Autonomic Fibers of the Auriculotemporal Nerve

机译:耳内多形神经纤维瘤起源于耳颞神经自主纤维的例外情况。

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摘要

Plexiform neurofibromas are benign tumors that tend to occur in patients suffering from neurofibromatosis type 1 (NF-1). This report addresses a rare case where the tumor affected the parotid gland, deriving almost exclusively from the peripheral portion of the facial nerve. A 6-year-old male was referred to us complaining about a gradually enlarging swelling over the right parotid area. Imaging localized the lesion to the superficial lobe of the parotid gland, suggesting a neurofibroma. Cosmetic disfigurement and a functional deficit led us to perform complete surgical resection. Meticulous surgical dissection as well as auriculotemporal nerve origin made complete extirpation possible with almost zero morbidity and ensured alleviation of both aesthetic impairment and pain. This is the first case of an intraparotid PN in a pediatric NF-1 patient, which originated from branches of the auriculotemporal nerve and particularly from fibers of the autonomic nervous system. Radical surgical excision was decided according to established decision-making algorithms.
机译:多形神经纤维瘤是一种良性肿瘤,易患1型神经纤维瘤病(NF-1)。该报告报道了一种罕见的病例,其中肿瘤几乎完全来自面神经的外围部分,影响了腮腺。一名6岁男性被转介给我们,抱怨右腮腺区域逐渐肿大。影像学检查显示病变位于腮腺浅叶,提示为神经纤维瘤。外观毁损和功能缺陷导致我们进行了完整的手术切除。细致的手术解剖以及耳颞神经起源使得完全切除的可能性几乎为零,并确保减轻了美学损伤和疼痛。这是小儿NF-1患者腮腺内PN的首例,其起源于耳颞神经的分支,尤其是植物神经系统的纤维。根据既定的决策算法决定根治性手术切除。

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