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Lower lip plexiform schwannoma: Report of a rare case and a literature review

机译:下唇丛状神经鞘瘤:一例罕见病例报告及文献复习

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摘要

Plexiform schwannoma is an uncommon benign neoplasm of the neural sheath characterized grossly and microscopically by multinodular growth. It is typically presented as a mobile, solitary, smooth-surfaced, and nontender mass. Histologically, schwannomas are classified into the following seven types: classical (Verocay), plexiform, cellular, cranial nerve, melanotic, degenerated (ancient), and granular cell schwannomas. In spite of the fact that plexiform schwannoma commonly occurs in the head-and-neck region, the involvement of the lip is considered to be extremely rare. Herein, we present the case of a 16-year-old boy with the schwannoma on the lower lip excised without any recurrence at 9 months after surgery.
机译:Plexiform schwannoma是一种罕见的神经鞘良性肿瘤,其特征是多结节性生长,在肉眼和显微镜下均可见。它通常以移动的,孤立的,表面光滑的且不招标的形式呈现。从组织学上讲,神经鞘瘤可分为以下7种类型:经典(Verocay),丛状,细胞,颅神经,黑素瘤,变性(古代)和颗粒细胞神经鞘瘤。尽管丛状神经鞘瘤通常发生在头颈部区域,但认为嘴唇受累极为罕见。本文介绍了一个16岁男孩的下唇神经鞘瘤切除术后9个月无复发的病例。

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