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眼眶粒细胞肉瘤表现为成人急性髓系白血病的暴发性眼眶病

Granulocytic Sarcoma of the Orbit Presenting as a Fulminant Orbitopathy in an Adult With Acute Myeloid Leukemia.

作者信息

O'Neill John P, Harrison Andrew R, Cameron J Douglas, Mokhtarzadeh Ali

机构信息

*Departments of Ophthalmology and Visual Neurosciences and †Department of Ophthalmology and Otolaryngology, University of Minnesota, Minneapolis, Minnesota.

出版信息

Ophthalmic Plast Reconstr Surg. 2017 May/Jun;33(3S Suppl 1):S118-S120. doi: 10.1097/IOP.0000000000000442.

Abstract

A 64-year-old woman with relapsed acute myelogenous leukemia (AML) undergoing salvage chemotherapy developed rapid onset of right-sided ophthalmoplegia, proptosis, optic neuropathy, and vision loss from 20/30 to hand motions over a 3-hour period on day 4 of her treatment. CT scan of her orbits revealed a superolateral orbital mass and periocular edema. She underwent immediate canthotomy and cantholysis, and lateral orbitotomy with debulking of the mass later the same day. The histopathology was consistent with aggregates of myeloid blasts. Her vision recovered to 20/20 on postoperative day 1. Orbital granulocytic sarcoma is a rare condition often concurrent with AML, typically in the pediatric population and rarely in adults. Presentation as a fulminant orbitopathy with rapidly progressive optic neuropathy and vision loss over several hours has not been previously reported.

摘要

一名64岁复发急性髓系白血病(AML)女性在接受挽救性化疗时,在治疗第4天的3小时内迅速出现右侧眼球运动麻痹、眼球突出、视神经病变,视力从20/30降至仅能识别手动。眼眶CT扫描显示眶上外侧有一肿块及眼周水肿。她立即接受了内眦切开和眦松解术,并于同一天晚些时候接受了外侧眼眶切开术及肿块减压术。组织病理学结果与髓母细胞聚集一致。术后第1天她的视力恢复到了20/20。眼眶粒细胞肉瘤是一种罕见疾病,常与AML并发,多见于儿童,成人罕见。此前尚未有过数小时内迅速进展为视神经病变和视力丧失的暴发性眼眶病的报道。

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