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格雷夫斯眼病中眼眶外周原始神经外胚层肿瘤——一种罕见的表现。

Peripheral primitive neuroectodermal tumor of the orbit in Graves' ophthalmopathy - A rare presentation.

作者信息

Stephen Mary A, Ahuja Shashi, Jayasri P, Harigaravelu P J

机构信息

Department of Opthalmology, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry, India.

Department of Surgery, Indira Gandhi Government General Hospital and Research Institute, Puducherry, India.

出版信息

Saudi J Ophthalmol. 2023 Mar 9;37(1):69-71. doi: 10.4103/sjopt.sjopt_143_21. eCollection 2023 Jan-Mar.

Abstract

Graves' ophthalmopathy is the most common cause of both unilateral and bilateral proptoses in adults. Peripheral primitive neuroectodermal tumor (pPNET) is a small round cell malignant lesion of neuroectodermal origin which very rarely affects the orbit. In this case report, we have discussed about a young woman with existing Graves' ophthalmopathy who presented with worsening proptosis; computed tomography imaging revealed an irregular mass lesion in the right orbit without bone erosion. Biopsy and immunohistochemistry of the mass lesion revealed features of primitive neuroectodermal tumor (PNET). The tumor was MIC-2 gene positive, and on follow-up, no recurrence was noted after successful surgical resection. PNET of the orbit is very rare, and to our best knowledge, this is the first case of peripheral PNET in patent with Graves' ophthalmopathy.

摘要

格雷夫斯眼病是成人单侧和双侧眼球突出最常见的病因。外周原始神经外胚层肿瘤(pPNET)是一种起源于神经外胚层的小圆细胞恶性病变,极少累及眼眶。在本病例报告中,我们讨论了一名患有格雷夫斯眼病的年轻女性,其眼球突出症状加重;计算机断层扫描成像显示右眼眶有一个不规则肿块病变,无骨质侵蚀。肿块病变的活检和免疫组织化学检查显示为原始神经外胚层肿瘤(PNET)的特征。该肿瘤为MIC-2基因阳性,随访发现成功手术切除后无复发。眼眶PNET非常罕见,据我们所知,这是首例合并格雷夫斯眼病的外周PNET病例。

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