起源于穆勒肌的眼眶白肌瘤:病例报告和文献综述。

IF 0.6 Q4 SURGERY International Journal of Surgery Case Reports Pub Date : 2024-11-01 Epub Date: 2024-10-16 DOI:10.1016/j.ijscr.2024.110466
Rakan Alsaad, Hind M Alkatan, Hatim Khoja, Adel Alsuhaibani
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引用次数: 0

摘要

简介眼眶白肌瘤可发生在眼眶的任何部位。后部肿瘤来自血管壁平滑肌细胞,而前部肿瘤则来自睑囊肌或 Muller 肌。眼科检查除发现上睑饱满、眼球向下和向外侧移位外,并无其他异常。核磁共振成像显示,患者右眼内侧眼眶内有一大片界限清晰的肿物。切除活检显示,该肿块易碎,与下层结膜和穆勒肌紧密粘连。本病例报告是根据 SCARE 标准编写和报告的:讨论:如果位于眼眶深部,眼眶良性肌瘤通常表现为进行性无痛性突眼。我们的患者由于肿瘤位于眼眶前部,主要表现为眼睑饱满和移位。眼眶细肌瘤的诊断必须通过组织病理学和免疫组化评估才能确诊,我们的病例就属于这种情况。我们利用从 1963 年到 2023 年的多个数据库进行了文献综述,得出的结论是男性患者居多。有一例与我们的病例类似,肿瘤起源于眶上神经血管束:据我们所知,这是英文文献中首次报道起源于穆勒肌的眼眶利肌瘤病例。
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Orbital leiomyoma originating from Muller muscle: A case report and review of the literature.

Introduction: Orbital leiomyoma can occur anywhere within the orbit. Posterior tumors arise from vessel wall smooth muscle cells, while anterior tumors develop from the capsulopalpebral or Muller muscle.

Presentation of case: we present a case of a 24-year-old man who was referred for evaluation of chronic right eye swelling involving the medial upper eyelid. Ophthalmologic examination was unremarkable apart from upper lid fullness along with downward and lateral displacement of the globe. MRI revealed a large and well-defined growth in the right medial orbital space. An excisional biopsy was performed which showed a friable mass strongly adherent to the underlying conjunctiva and Muller muscle. This case report has been prepared and reported in line with the SCARE criteria.

Discussion: Orbital leiomyoma usually presents with progressive painless proptosis if situated deep in the orbit. Our patient presented mainly with eyelid fullness and displacement due to the anterior location of his tumor. The diagnosis of orbital leiomyoma has to be confirmed by histopathological and immunohistochemical assessments such as in our case. A literature review was conducted using multiple databases spanning from 1963 to 2023 which concluded male predominance. One similar case to ours has been reported with the tumor originating from supraorbital neurovascular bundle.

Conclusion: To the best of our knowledge, this is the first reported case of an orbital leiomyoma originating from the Muller muscle in the English literature.

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