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一名青少年男性患者,眶下神经鞘瘤表现为上唇肿物。

Infraorbital nerve schwannoma presenting as an upper lip mass in an adolescent boy.

作者信息

Kok Yee Onn, Yeo Matthew Sze-Wei, Nallathamby Vigneswaran, Lee Shu Jin

机构信息

Ministry of Health Holdings, Department of Surgery, National University Hospital, Singapore.

出版信息

Ann Plast Surg. 2013 Aug;71(2):196-7. doi: 10.1097/SAP.0b013e318248b8a2.

Abstract

BACKGROUND

Schwannomas of the head and neck are uncommon tumors that arise from the nerve sheath and may afflict peripheral, autonomic, or cranial nerves. It is important to consider the possible differential diagnoses of a nasolabial lump in a child because its appropriate treatment varies widely.

METHODS

The authors describe a case of a 12-year-old boy who presented with a 2.5-cm right nasolabial subcutaneous lump of 3 months in duration. Computed tomographic scan showed a homogeneously attenuated lesion.

RESULTS

An intraoral incision was used for complete extirpation of this tumor while preserving the infraorbital nerve and facial aesthetics in this adolescent boy. Histopathologic examination showed palisades of spindle cells and Verocay bodies characteristic of schwannomas. The patient has been followed up for 2 years with no clinical evidence of recurrence.

CONCLUSIONS

Only 9 cases of infraorbital nerve schwannoma have been described in literature, and the sublabial intraoral incision was attempted in only 1 case. The authors describe a rare case of an extraosseous schwannoma arising from the infraorbital nerve that presented as a cheek lump, its workup, its differentials, its treatment, and a review of literature. The use of a preoperative computed tomographic scan permitted the use of a sublabial intraoral incision with good visual access to the lesion and facilitated its complete extirpation without incurring external scars.

摘要

背景

头颈部神经鞘瘤是一种罕见的肿瘤,起源于神经鞘,可累及周围神经、自主神经或颅神经。考虑儿童鼻唇肿块的可能鉴别诊断很重要,因为其适当的治疗方法差异很大。

方法

作者描述了一例12岁男孩,其右鼻唇皮下出现一个持续3个月的2.5厘米肿块。计算机断层扫描显示为均匀低密度病变。

结果

在这名青少年男孩中,采用口内切口完整切除了该肿瘤,同时保留了眶下神经和面部美观。组织病理学检查显示为神经鞘瘤特有的梭形细胞栅栏状排列和Verocay小体。患者已随访2年,无复发的临床证据。

结论

文献中仅描述了9例眶下神经鞘瘤,仅1例尝试采用唇下口内切口。作者描述了一例罕见的起源于眶下神经的骨外神经鞘瘤,表现为颊部肿块,包括其检查、鉴别诊断、治疗方法以及文献复习。术前计算机断层扫描的应用使得可以采用唇下口内切口,能很好地直视病变并便于完整切除,且不会留下外部疤痕。

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