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冯雷克林霍增氏神经纤维瘤病中的葡萄膜恶性黑色素瘤和视神经胶质瘤。

Uveal malignant melanoma and optic nerve glioma in von Recklinghausen's neurofibromatosis.

作者信息

Antle C M, Damji K F, White V A, Rootman J

机构信息

Department of Pathology, Vancouver General Hospital, British Columbia, Canada.

出版信息

Br J Ophthalmol. 1990 Aug;74(8):502-4. doi: 10.1136/bjo.74.8.502.

Abstract

A case of uveal malignant melanoma and contralateral optic nerve glioma is described in a 53-year-old Caucasian male with multiple uveal melanocytic hamartomas and neurofibromatosis. The eye was enucleated, and histologically the melanoma was found to consist of 70% epithelioid cells, with many bizarre, multinucleated forms. CT scan demonstrated a non-enhancing, fusiform enlargement of the contralateral optic nerve with enlargement of the optic canal and intracranial extension. This combination of tumours has not previously been reported in a patient with neurofibromatosis and serves to emphasise the common neuroectodermal origin of tumours in this autosomal dominant condition.

摘要

本文描述了一名53岁患有多发性葡萄膜黑素细胞错构瘤和神经纤维瘤病的白种男性患者,其患有葡萄膜恶性黑色素瘤及对侧视神经胶质瘤。该眼已被摘除,组织学检查发现黑色素瘤由70%的上皮样细胞组成,有许多形态怪异的多核细胞。CT扫描显示对侧视神经呈无强化的梭形增粗,视神经管扩大并向颅内延伸。这种肿瘤组合此前尚未在神经纤维瘤病患者中报道过,这进一步强调了在这种常染色体显性遗传病中肿瘤的共同神经外胚层起源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ed5/1042186/dd8e73cc0b0b/brjopthal00582-0055-a.jpg

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