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磁共振成像显示筛窦起源的眶粘液瘤切除术:病例报告及文献复习 20 例。

Resection of Orbital Myxoma With Magnetic Resonance Imaging Evidence of Ethmoid Sinus Origin: Case Report and Review of 20 Patients in the Literature.

机构信息

Okayama University, Japan.

Okayama University Hospital, Japan.

出版信息

J Investig Med High Impact Case Rep. 2023 Jan-Dec;11:23247096231201013. doi: 10.1177/23247096231201013.

Abstract

A 41-year-old woman showed a palpable mass at the superonasal orbital edge on the right side. Magnetic resonance imaging demonstrated a lobulated fluid-containing tubular mass which extended anteriorly to posteriorly along the medial orbital wall, nasal to the eyeball. She was followed once a year for 8 years until the age of 49 years when she decided to undergo surgical resection because of the enlarged mass. The lobulated large mass was resected and the pathology showed sparsely distributed spindle cells, positive for CD34, in alcian blue-positive mucous substances, indicative of myxoma. Postoperative magnetic resonance imaging showed residual lobulated tubular mass along the optic nerve on the medial side and superior to the eyeball. The residual orbital mass showed stable structure with more evident connection with the ethmoid sinus lesion, suggestive of the ethmoid origin, in 12 years until the age of 61 years. In the review of 20 patients with orbital myxomas in the literature, in addition to this case, roughly classified locations in the orbit were retrobulbar in 8 patients, on the lateral side of the orbit in 4, on the superior side in 6, on the medial side in 1 (this patient), and in the orbit with no specific description in 2. In pathological examinations, immunohistochemistry was not done in 8 patients, done but all negative in 2, and positive in 11 patients: nerve sheath myxoma was diagnosed in 3 patients based on positive S100 staining. Orbital myxoma is rare but considered in differential diagnosis of orbital masses.

摘要

一位 41 岁女性右侧额窦眶上缘触及一可触及肿块。磁共振成像显示一呈分叶状含液管状肿块,从前向后沿眶内侧壁延伸,位于眼球鼻侧。她每年随访一次,共随访 8 年,直到 49 岁时,由于肿块增大,决定行手术切除。切除分叶状大肿块,病理显示稀疏分布的梭形细胞,在阿尔辛蓝阳性黏液物质中 CD34 阳性,提示为黏液瘤。术后磁共振成像显示视神经内侧和眼球上方残留分叶状管状肿块。残留眶内肿块结构稳定,与筛窦病变连接更明显,提示起源于筛窦,随访 12 年,直至 61 岁。在回顾 20 例眼眶黏液瘤患者的文献中,除本例外,大致将病变位置分类为:球后 8 例,眶外侧 4 例,眶上侧 6 例,眶内侧 1 例(本例),眶内无特定描述 2 例。在病理检查中,8 例未行免疫组化检查,2 例均为阴性,11 例为阳性:3 例基于 S100 染色阳性诊断为神经鞘黏液瘤。眼眶黏液瘤罕见,但被认为是眼眶肿块的鉴别诊断之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a140/10517617/0796898f986a/10.1177_23247096231201013-fig1.jpg

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