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一例罕见的腋窝神经鞘瘤。

A rare case of axillary Schwannoma.

作者信息

Sengul Demet, Sengul Ilker, Karinoglu Uygar, Apan Ozgun Cuvas, Oksuz Hulya, Apan Alparslan

出版信息

Ann Ital Chir. 2019 Jun 3;8:S2239253X19030470.

Abstract

Schwannoma, neurilemmoma, is well capsulated, slowly growing tumor originating from benign neoplastic Schwann cells of the peripheral nerve sheath. Due to its rarity and complex anatomical location they can pose the misdiagnosis at clinical evaluation. A total surgical excision with a safety margin was performed for 63 year-old male with the complaints of painless lump at the axillary region for 4 months and the diagnosis of axillary Schwannoma confirmed by the histopathological examination and immunohistochemistry. Although its rarity, Schwannoma should be kept in mind for the differential diagnosis of axillary masses. Its complete resection represents the cure for indicated cases. KEY WORDS: Axilla, Immunohistochemistry, Peripheral Nerve Sheath, Schwannoma.

摘要

施万细胞瘤,即神经鞘瘤,是一种包膜完整、生长缓慢的肿瘤,起源于周围神经鞘的良性肿瘤性施万细胞。由于其罕见性和复杂的解剖位置,在临床评估中可能会出现误诊。对一名63岁男性进行了带安全切缘的完整手术切除,该患者因腋窝区域无痛性肿块4个月前来就诊,组织病理学检查和免疫组化确诊为腋窝施万细胞瘤。尽管施万细胞瘤罕见,但在腋窝肿块的鉴别诊断中应予以考虑。对于合适的病例,完整切除可实现治愈。关键词:腋窝;免疫组化;周围神经鞘;施万细胞瘤

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