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葡萄膜丛状色素性神经鞘瘤

Plexiform pigmented schwannoma of the uvea.

作者信息

Saavedra Egbert, Singh Arun D, Sears Jonathan E, Ratliff Norman B

机构信息

Cole Eye Institute, Cleveland Clinic Foundation, Ohio 44195, USA.

出版信息

Surv Ophthalmol. 2006 Mar-Apr;51(2):162-8. doi: 10.1016/j.survophthal.2005.12.004.

Abstract

Schwannoma is a slow growing solitary tumor that preferentially involves spinal nerve roots, and sympathetic, cervical, and vagus nerves. There are several clinico-pathologic variants of schwannoma, including schwannoma with a degenerative change (ancient schwannoma), cellular schwannoma, plexiform schwannoma, epithelioid schwannoma, and melanotic schwannoma. About 10% of cases of schwannomas are associated with multi-system disorders such as neurofibromatosis, schwannomatosis, multiple meningiomas, and Carney complex. Schwannoma rarely present as an intraocular tumor and is often misdiagnosed as malignant melanoma. Immunohistochemical positivity with S-100 stain and demonstration of long-spaced collagen (Luse bodies) are helpful in establishing the diagnosis. In this article, we review the clinical and histopathological findings of a sporadic plexiform pigmented schwannoma involving the iris, ciliary body, and the choroid.

摘要

施万细胞瘤是一种生长缓慢的孤立性肿瘤,主要累及脊神经根以及交感神经、颈神经和迷走神经。施万细胞瘤有多种临床病理变体,包括伴有退行性改变的施万细胞瘤(陈旧性施万细胞瘤)、细胞性施万细胞瘤、丛状施万细胞瘤、上皮样施万细胞瘤和黑色素性施万细胞瘤。约10%的施万细胞瘤病例与多系统疾病相关,如神经纤维瘤病、施万细胞瘤病、多发性脑膜瘤和卡尼综合征。施万细胞瘤很少表现为眼内肿瘤,常被误诊为恶性黑色素瘤。S-100染色免疫组化阳性以及长间距胶原(卢斯小体)的显示有助于确诊。在本文中,我们回顾了一例累及虹膜、睫状体和脉络膜的散发性丛状色素性施万细胞瘤的临床和组织病理学表现。

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