Kajeou Meriem, Almaghribi Israe, Arkha Yasser
Departments of Neurosurgery, Mohammed V University of Rabat, Hospital of Specialities-Rabat, Rabat, Morocco.
Surg Neurol Int. 2025 Jun 6;16:233. doi: 10.25259/SNI_201_2025. eCollection 2025.
Orbital leiomyoma is a rare benign tumor of the smooth muscles of the orbit with intraconal or extraconal location. The tumor affects twice as many men as women, with an average age of 30 years.
A 38-year-old female presented with proptosis: Axile, nonpulsatile, painless, nonreducible, Grade III, with impairment of oculomotricity, associated with a decrease in visual acuity on the affected side with an AV at 03/10, and fundus: Grade I papilledema. The computed tomography scan showed a solitary, tissue mass, well-limited, encapsulated, and usually homogeneous, with homogeneous enhancement after contrast injection. The magnetic resonance imaging showed a rounded, homogeneous lesion, isointense on T1 and hyperintense on T2, with homogeneous enhancement after gadolinium injection. Suggestive of an intraorbital cavernous hemangioma. The patient underwent surgery via a subfrontal approach, with macroscopically complete resection. Histopathological examination was in favor of an orbital leiomyoma.
Although very rare, orbital leiomyoma should be considered in the differential diagnosis of patients with orbital tumors.
眼眶平滑肌瘤是一种罕见的眼眶平滑肌良性肿瘤,可位于肌锥内或肌锥外。该肿瘤男性患者的发病率是女性的两倍,平均发病年龄为30岁。
一名38岁女性患者出现眼球突出:轴性、非搏动性、无痛、不可复位,Ⅲ级,伴有眼球运动障碍,患侧视力下降,视力为0.3,眼底:Ⅰ级视乳头水肿。计算机断层扫描显示一个孤立的组织肿块,边界清晰,有包膜,通常均匀一致,注射造影剂后均匀强化。磁共振成像显示一个圆形、均匀的病变,T1加权像上等信号,T2加权像上高信号,注射钆剂后均匀强化。提示眶内海绵状血管瘤。患者通过额下入路接受手术,肉眼下完全切除。组织病理学检查结果支持眼眶平滑肌瘤的诊断。
尽管眼眶平滑肌瘤非常罕见,但在眼眶肿瘤患者的鉴别诊断中应考虑到该疾病。