侵袭性眼眶鳞状细胞癌合并多发性骨髓瘤1例。

IF 0.7 Q4 OPHTHALMOLOGY
Case Reports in Ophthalmological Medicine Pub Date : 2022-06-29 eCollection Date: 2022-01-01 DOI:10.1155/2022/8585692
Narges Karrabi, Kiana Hassanpour, Noushin Afshar Moghaddam, Faezeh Khorasanizadeh, Sadid Hooshmandi, Amirreza Veisi
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引用次数: 4

摘要

背景:眼眶鳞状细胞癌(SCC)是一种罕见的肿瘤。它通常是SCC起源于皮肤、鼻咽部、鼻腔、鼻窦、结膜、泪腺或囊的局部侵袭的结果,或较少通过血液转移发生。在此,我们报告一位眼眶鳞状细胞癌合并多发性骨髓瘤(MM)病史的患者。案例演示。一名45岁女性,过去两年有MM病史,主诉右眼逐渐突出6个月。在检查中发现右眼瞳孔相对传入缺损。右眼的眼球运动在各个方向上都受到限制。眼眶磁共振显示右眼眶浸润性肿块,从眶前延伸至眶尖及视神经管。患者进行了减积,组织病理学检查显示SCC结果。没有发现其他继发部位是肿瘤的起源。结果:患者接受了化疗和放疗。据我们所知,这是首次报道合并MM和原发性眼眶SCC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Invasive Orbital Squamous Cell Carcinoma in a Patient with Multiple Myeloma.

Invasive Orbital Squamous Cell Carcinoma in a Patient with Multiple Myeloma.

Invasive Orbital Squamous Cell Carcinoma in a Patient with Multiple Myeloma.

Background: Orbital squamous cell carcinoma (SCC) is a rare entity. It is often a result of local invasion of SCC originating from the skin, nasopharynx, nasal cavity, paranasal sinuses, conjunctiva, lacrimal glands, or sac or less commonly occurs through hematogenous metastasis. Herein, we report a patient with orbital SCC with a history of multiple myeloma (MM). Case presentation. A 45-year-old woman with a history of MM in the past two years presented to our clinic complaining of gradual right eye proptosis for six months. The relative afferent pupillary defect was detected in the right eye on her examination. Ocular movements of the right eye were limited in all directions. Orbital magnetic resonance imaging demonstrated an infiltrative mass in the right orbit extended from the anterior to the orbital apex and the optic canal. The patient underwent debulking, and a histopathology examination revealed SCC results. No other secondary site was found to be the origin of the tumor.

Result: The patient underwent chemotherapy and subsequent radiotherapy. To our knowledge, this is the first report of concomitant MM and primary orbital SCC.

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