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下唇丛状神经鞘瘤:1例罕见病例报告及文献复习

Lower Lip Plexiform Schwannoma: Report of a Rare Case and a Literature Review.

作者信息

Yaghoobi Reza, Pazyar Nader

机构信息

Department of Dermatology, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

出版信息

Indian J Dermatol. 2019 Sep-Oct;64(5):407-410. doi: 10.4103/ijd.IJD_207_18.

Abstract

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.

摘要

丛状神经鞘瘤是一种罕见的神经鞘良性肿瘤,其大体和显微镜下特征为多结节生长。它通常表现为可移动的、孤立的、表面光滑且无压痛的肿块。组织学上,神经鞘瘤分为以下七种类型:经典型(Verocay型)、丛状型、细胞型、颅神经型、黑色素型、退化型(陈旧型)和颗粒细胞型神经鞘瘤。尽管丛状神经鞘瘤常见于头颈部区域,但唇部受累被认为极为罕见。在此,我们报告一例16岁男孩下唇神经鞘瘤的病例,术后9个月切除,无任何复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61e3/6749764/471822c6955b/IJD-64-407-g001.jpg

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